| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs111475972 | snp | C/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147437 | GAACAAGTATTTCCC[C/G]TACCCTGGATACTTA | 57630 |
| rs111490639 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142429 | CTTTTCATTCCACAA[C/T]TGTTTTAAATAAGAA | 57630 |
| rs111494087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128310 | ATCTCAGGGAAACCA[A/G]ATTTCACTAAAAGTT | 57630 |
| rs111535427 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187233 | AAACAGGGTCTCACC[A/G]TGTCACCCAGGCTAG | 57630 |
| rs111549277 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109577 | ATGCTTTCAATGGCA[C/T]ATTCTGATTTTTTCT | 57630 |
| rs111551385 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117359 | TAATACGCAGGGCAC[A/G]CTTAGCCCAAATAAG | 57630 |
| rs111563643 | snp | A/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153244 | CATAAGACATAGTGG[A/T]GTCAGACCCTTGGAG | 57630 |
| rs111604308 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145958 | TATTATTCTATATAA[A/T]ATATTACATATTCTA | 57630 |
| rs111616794 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272484 | AATAATAGCCCACTT[C/T]CCCTTCCATTAGAAG | 57630 |
| rs111641288 | in-del | -/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208150 | ATTTAAGTCCTCAAG[-/T]TTTTTTTTTTTTTCC | 57630 |
| rs111777989 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104091 | TAAGAGGAAGGGACC[A/G]GAATGCAGAAGCCGT | 57630 |
| rs111828535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183373 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC | 57630 |
| rs111836307 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121972 | AGGTAGAAGTTTGCA[G/T]GACACAGACCGCTTG | 57630 |
| rs111837776 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131435 | TTCTTATTAGACAGA[A/G]TCTCACTATGTTGAG | 57630 |
| rs111843679 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253965 | ATTTCTAGACCACCA[C/T]GGTGGGTGCAACCAA | 57630 |
| rs111865368 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123708 | CATTTTGGCTAACAC[A/G]GTGAAACCCCATCTC | 57630 |
| rs111887776 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157023 | ACTCATAAAAAACAA[A/G]CTTAACTTCCTACAT | 57630 |
| rs111897560 | in-del | -/A | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239866 | ACCCCGTCTCTAATG[-/A]AAAAAAATACAAAAA | 57630 |
| rs111902917 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267734 | ATTCTGTTAAAACTG[C/T]CTGGTATCCACATCT | 57630 |
| rs111925768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199804 | TATAAATAAAATATT[A/G]AGGTAAGGTGACAGT | 57630 |
| rs111930024 | snp | A/C | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217862 | CATTTTACCAAAAAA[A/C]AAAAAAAAGTTTAAT | 57630 |
| rs111932102 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250964 | GTGCAAAGGCCCTAG[A/G]CTTTGGTGGTTTGAT | 57630 |
| rs112001275 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183367 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 57630 |
| rs112001485 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243382 | GCTAGGCATTACAGC[A/G]CATGCCTGTAATCCC | 57630 |
| rs112032371 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097889 | AAACTGGCTGCCATG[C/T]TGTGAGGACACTCAA | 57630 |
| rs112043424 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109962 | AGTTGCAGTGAGCTA[C/T]GACCATGCCACTGCA | 57630 |
| rs112057793 | snp | A/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229031 | CTGATTTATTTTTTT[A/T]AAAAAAGGCATGACA | 57630 |
| rs112079816 | snp | G/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154840 | AATGAAAATCTACTA[G/T]GAATTGTAACTCCTT | 57630 |
| rs112099272 | snp | C/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238685 | TCAAGGTTTGTTCTT[C/G]CACATGGTCTAACTG | 57630 |
| rs112115531 | in-del | -/T | 0.154572 | 0.23107 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114526 | AGTCACTATTCTGTC[-/T]TATCACAAGTACCTT | 57630 |
| rs112166659 | snp | A/C | 0.0260105 | 0.111035 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271692 | CCGCGGCCACCTGTC[A/C]GCACCCAGCCATCAG | 57630 |
| rs112168666 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264047 | GGATTGGCAGTGGAC[C/T]GAGAGGCCACTCAAG | 57630 |
| rs112170913 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230520 | TATTTCAATCTAAAA[C/T]AAAAAATCTCAAAGC | 57630 |
| rs112198424 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191888 | CTTATACACAAATCA[A/G]CTCAAGATGGATTAA | 57630 |
| rs112219572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208331 | GCCCACTGGAACACA[C/T]TGTGCCCTCATTTTC | 57630 |
| rs112245330 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242359 | GCAATGTTTTTAAAA[C/T]GAAATATCGCTTCTA | 57630 |
| rs112257921 | snp | A/G | 0.159622 | 0.233092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193008 | ATGAGACTGGATACT[A/G]TTATTCTAAGTGAAG | 57630 |
| rs112291274 | in-del | -/AT | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206262 | CTTAGCATGCCACAC[-/AT]GATTCAATCTAAAAT | 57630 |
| rs112321683 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250685 | TGCCTATTGTGGGGT[A/G]GTGGGGATGGGGGTA | 57630 |
| rs112339706 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121172 | TGCTGTCTACATTTT[A/G]AAAGTAGGCAGAGGC | 57630 |
| rs112339823 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130010 | ACATGACTAAAGACC[C/T]AAAAGAGAAATAAAA | 57630 |
| rs112346162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156796 | CACACTGTAACCCTT[G/T]AAGAAAATCTCACAC | 57630 |
| rs112349004 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203235 | GCATCTTGCTCTTTG[C/T]AGTTGAAAGAGCAAA | 57630 |
| rs112366388 | in-del | -/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141639 | GACTGATATAAATAC[-/T]TTTTTTTTTTTTTTT | 57630 |
| rs112419785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140406 | CTAAAATACCTTCTT[C/T]CAAGCATTTGGTAAG | 57630 |
| rs112422892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126080 | TGTAAATTGTCTTTC[C/T]CAGTGCCCTGGAACA | 57630 |
| rs112428795 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102952 | TTTGAGATGGAGTCT[C/T]GCTCTGTCAGGCTGG | 57630 |
| rs112440351 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118193 | TTGCCTCCAGCTCCA[C/T]ATCACACATGTGCCC | 57630 |
| rs112459313 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254251 | GAACTGACCACCTAC[C/T]ACTTTTTCCACAGTC | 57630 |
| rs112463525 | snp | C/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155877 | TAGCCTCCTGAGTTT[C/G]TTTTAGATTGATTCT | 57630 |
| rs112475560 | snp | A/C | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112828 | GAAACAAGAAGAACA[A/C]GAAAGACACAGACCC | 57630 |
| rs112494565 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170705 | CTTCATTCCATCCTA[C/T]ATAGATCTGCCAGAT | 57630 |
| rs112545034 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148500 | TACCAAAATTATACA[C/T]GATGAGACTTAGGAT | 57630 |
| rs112549843 | snp | G/T | 0.120326 | 0.21374 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249977 | AAAAAACGATTATCT[G/T]AAGTCTGATTTGAAT | 57630 |
| rs112555385 | snp | C/G | 0.130008 | 0.219321 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183362 | CCTGGCTCACTGCAA[C/G]CTCCGCCTCCCGGGT | 57630 |
| rs112567672 | snp | C/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267751 | TGGTATCCACATCTG[C/T]GAATTATGGGAACTA | 57630 |
| rs112578159 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250364 | TTTTAAATCATTCCA[C/T]ATTTATCTTCATAAA | 57630 |
| rs112613790 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148504 | AAAATTATACACGAT[A/G]AGACTTAGGATTATT | 57630 |
| rs112631874 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204707 | AGGCATGCACTACCA[C/T]GCCCGGCTAATTTTT | 57630 |
| rs112634154 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141337 | CATCTTTGCATATCA[A/G]TAGGGATAGGCTGAT | 57630 |
| rs112663895 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139927 | TGTATAATGCATAAT[C/T]TCACTTTAAATGGAC | 57630 |
| rs112678817 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174841 | GACTCTCATATGAAG[C/T]GCTAAGAACTGTGGA | 57630 |
| rs112682025 | snp | C/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157860 | ATTTTAACGCTTCAG[C/G]CTCCCAAGTAGCTGG | 57630 |
| rs112686588 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165135 | CACAGGATGGGGACT[A/G]TTTCCTGGGAAAAGG | 57630 |
| rs112705247 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145181 | AGTCACGAAATCAAC[C/T]TGAGTGTCCATCAAC | 57630 |
| rs112707974 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141844 | TTGAGATGGAGTCTC[A/G]CTCTGTTGCCCAGGC | 57630 |
| rs112721072 | snp | A/C | 0.164219 | 0.234823 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231389 | TGACCAATATGGTGA[A/C]ACCCAGTCTCTACTA | 57630 |
| rs112728042 | snp | C/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179421 | TAAAATTACTTTGTA[C/G]TTTTAAGCCATTGAA | 57630 |
| rs112741265 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252134 | CTTAAGAGGGCCTGC[A/G]TTTTCACATTTTATA | 57630 |
| rs112743893 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261402 | AGATTCCCCTGCTAA[A/G]AGCAACATGAGGTCC | 57630 |
| rs112766244 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238770 | GAAAACATTTCAGCT[A/G]CCCTAATATATTGCT | 57630 |
| rs112827438 | snp | C/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271790 | CGGTAGTACGGACTT[C/G]CAACCCAGGCTCGGG | 57630 |
| rs112840513 | snp | G/T | 0.0360663 | 0.129354 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193064 | TTGTATGTTCTCACT[G/T]ATAAGTGGGAGCTAA | 57630 |
| rs112861957 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223947 | GCTGGAAGAAAATAC[A/G]TGAATCAAAGAGGTA | 57630 |
| rs112933907 | in-del | -/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113112 | TTTTCTTTTTTTTTT[-/T]CCCCCCTGAGACAGA | 57630 |
| rs112944475 | snp | C/G | 0.107694 | 0.205546 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248422 | TGTTCTCACTCATAA[C/G]TGGGAGTCGAATAAT | 57630 |
| rs112971153 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110096 | ATGAACGTTAGAGGC[C/T]GGGCACAGTGGCTTA | 57630 |
| rs112976591 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154340 | GATTTTTTATGAAAA[C/T]GTTGGCAATCTCACT | 57630 |
| rs112976893 | snp | A/T | 0.130008 | 0.219321 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183370 | ACTGCAACCTCCGCC[A/T]CCCGGGTTCAAGTGA | 57630 |
| rs112998703 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126811 | GCCCATGCTGGTCTC[A/G]AACTCCTGGCCTCAA | 57630 |
| rs113001434 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146671 | CTAACACTAACTGCA[A/G]GGAGTAAGAAAGCAG | 57630 |
| rs113013678 | in-del | -/A | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100689 | CAGCTACCCACTGCC[-/A]AAAAAATCATTAACA | 57630 |
| rs113038353 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242863 | TGGACTTCCCAGCCT[C/T]CAGAACCATGAGCCA | 57630 |
| rs113068066 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182057 | TAGTAGGCACTCAAT[G/T]TTTGTTGCAGAAATA | 57630 |
| rs113079806 | snp | A/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163347 | CAGAAAACAAACTGA[A/T]ATACATTTGTCCCAC | 57630 |
| rs113096475 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253230 | TACCAAACCTTCCTA[A/G]CATGTTGCTTCTCAA | 57630 |
| rs113138800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240531 | TAAGAAAGCAGTTTG[A/G]GAAACTGTTCAATTT | 57630 |
| rs113151286 | snp | C/T | 0.444444 | 0.157135 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175865 | AAACCCTAACCAGTG[C/T]GAGAGTATTTGGAGG | 57630 |
| rs113165277 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203055 | TCTGAGAAGTTCTGC[A/G]GCAAAGAAACCTGTT | 57630 |
| rs113167750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259042 | AAACTAGATATGAAG[C/T]ATCCTATAGCTAACT | 57630 |
| rs113174518 | snp | A/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204303 | AACTAATTCAATGAA[A/T]TTCCAGCACCTCATT | 57630 |
| rs113183020 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143582 | ATGACTCCCCTGACT[C/T]CCTATGGCCCACATT | 57630 |
| rs113215011 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098955 | AGAGGCCTGGCACTT[C/T]AAGGAGGTGAAGAAT | 57630 |
| rs113233932 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145458 | TTTACCTATTGGGTA[C/G/T]GATGTTCACCATGTG | 57630 |
| rs113254110 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198824 | CTTCAACGGAAACAA[C/T]AGAGGCCAATGGTTT | 57630 |
| rs113263674 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249993 | AAGTCTGATTTGAAT[C/T]CACACTATATCAAAT | 57630 |
| rs113294361 | snp | A/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157743 | AAGCTTTTACTTTTT[A/T]TTTCTTTTTTTTTTT | 57630 |
| rs113297251 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125064 | AACAATATTCTGCTC[A/C]CCAAAACTAGGACTT | 57630 |
| rs113306660 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238150 | TGTAATACTCTAATG[C/T]AATATAGTCTTCAAT | 57630 |
| rs113321927 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195133 | AAAATTTTCCAGTTT[G/T]GCTGAAAATGTCTTT | 57630 |
| rs113326959 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146264 | AGACCAAGTCTCGCT[C/T]TGTAGCCCAGGCTGC | 57630 |
| rs113335119 | snp | C/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157863 | TTAACGCTTCAGCCT[C/G]CCAAGTAGCTGGGAT | 57630 |
| rs113350622 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180082 | ACAAAAGAAAAAACT[G/T]GTAGTTCCAGTGCTG | 57630 |
| rs113377416 | in-del | -/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111432 | GCTAATTAAAAATAA[-/T]TTTTTTTTTTTTGGT | 57630 |
| rs113385619 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160598 | ATCTAACCCATGAAC[A/G]AACATTTGTGCATCT | 57630 |
| rs113386553 | snp | C/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152234 | AAGAGAGGTCTGAAA[C/G]AATCTCCGGAGGGGA | 57630 |
| rs113422209 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241184 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 57630 |
| rs113442723 | snp | C/G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224127 | AATTTAGAAGCTCCA[C/G/T]TAATTTCTAAACACT | 57630 |
| rs113472843 | snp | A/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112783 | AAAGACAAAAAAAAA[A/T]TTTGTAAGAGCTCTT | 57630 |
| rs113473503 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133503 | AAAAAAGAGGCTGTG[C/T]GTGGTGGCTCACACC | 57630 |
| rs113474481 | snp | C/T | 0.5 | 0 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093922 | TTATCATACTATTGG[C/T]TGATAGGTCTGCTTT | 57630 |
| rs113542375 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259515 | CTAGGCATTGGCAGA[C/T]ATATACGCGACAAAA | 57630 |
| rs113543224 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206263 | TTAGCATGCCACACA[C/T]GATTCAATCTAAAAT | 57630 |
| rs113550040 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181496 | TCGATCTCCTGACCT[C/T]ATGATCCACCCGCCT | 57630 |
| rs113566500 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268476 | TGTAATTATGACTCT[C/G]AGCCCCATCAAAATG | 57630 |
| rs113608345 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120596 | ACTTAAAACCCAGTA[C/G/T]ATTTACTGGTAGAAA | 57630 |
| rs113687926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175113 | GATGCCTCCGTTCCC[A/C]TTCTTTCACATTGCA | 57630 |
| rs113700302 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122862 | TTGGTACTATCGAGG[C/T]TGGTAATCTTTAACA | 57630 |
| rs113715183 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157742 | CAAGCTTTTACTTTT[C/T]TTTTCTTTTTTTTTT | 57630 |
| rs113734802 | snp | C/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164131 | TGAATACTGTTATCA[C/T]GGCCCTTATCTTACT | 57630 |
| rs113737971 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145785 | ATATTATATATTCTA[A/T]ATATTATTCTATATA | 57630 |
| rs113758971 | in-del | -/AAAC | 0.0444908 | 0.142359 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262986 | AACATGGTTTAGCCA[-/AAAC]AAACAAACAAACAAA | 57630 |
| rs113772966 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136810 | TTGTATCTATATCAC[A/G]GGTAGATATTAAATC | 57630 |
| rs113794102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200569 | GAATCAGAAACATAA[C/T]GTGAGGAAAAAAACA | 57630 |
| rs113801214 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105258 | AAAACAGATGACACT[G/T]AAGACAAATACTATA | 57630 |
| rs113801242 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256570 | TTACCAGACTACATA[C/T]ACACCAATAGTCTGT | 57630 |
| rs113809948 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147285 | ACCAGATGTAGGGAT[A/G]CTATAAAAGAAATAT | 57630 |
| rs113840035 | snp | A/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166523 | GTTGAAAAGAAAAAG[A/G]AGAAAGTTCTTGCAA | 57630 |
| rs113842713 | in-del | -/CTCTAA | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204051 | GTCTCTCTTCACTCC[-/CTCTAA]CTCTAACTCATTTTA | 57630 |
| rs113901714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149252 | TTACCTAAACAACTC[A/C]TTTTTAGATTGAGTC | 57630 |
| rs113908575 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121824 | AGTATTCTTATGCAA[G/T]AAATGAAAATAAAGA | 57630 |
| rs113934068 | snp | G/T | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168969 | AATCAAATCAAGCCA[G/T]CTTCAATACTCCAAA | 57630 |
| rs113987875 | in-del | -/G | 0.5 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098677 | ATAGACCACAAGGCT[-/G]GGGTTTGATCAAGCA | 57630 |
| rs114036592 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140929 | TAGCCCAACACAAAT[C/T]TGTAAACTTTCTTAA | 57630 |
| rs114054468 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173447 | GATTAAAAAAAAAAA[A/G]GTAGCAAAAGAACAC | 57630 |
| rs114074067 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260140 | GGGGCTCGTGGAATG[C/G]TGAGAAAAGACCACA | 57630 |
| rs114086129 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213253 | CCTGGTGGTAGCTCA[C/G]TTTAATCTGCATTCC | 57630 |
| rs114098947 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137134 | ATGTGCTTCCATGTA[A/T]ATTTACCTCCTGCCT | 57630 |
| rs114110423 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240355 | GCACAAACCACCATG[C/T]CCGCCTGATTTTTTT | 57630 |
| rs114141959 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207609 | ATTCTGTCCATAGTA[C/T]GTGGTCAGCTCTGCA | 57630 |
| rs114144112 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211645 | CAAATGAAGGCCTGC[A/G]TGCTTCTAGAGCATT | 57630 |
| rs114199661 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140464 | TAAGGTAAAATTCAG[A/T]ATACTGGAGATAAAA | 57630 |
| rs114202083 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100875 | CCTTTACTTCCCCCA[C/T]GCCACACCTTGGCTC | 57630 |
| rs114263787 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240913 | TGCAAGGAAGCCTTT[C/T]AAGTGAAGTGAAGCT | 57630 |
| rs114283461 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172104 | AGGTAGAAGTACTCT[A/G]AATTTTCCACTCTGA | 57630 |
| rs114310691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113932 | AGGAGATCTGCATTT[C/T]CTATGTGGGCCCTCA | 57630 |
| rs114359946 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220696 | TCAAACAACTGACCC[A/G]CAAACTCTATAGTTA | 57630 |
| rs114360054 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129475 | TGTTTTTAAGCAATT[A/T]GCCGTTTAGACTCTA | 57630 |
| rs114486555 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144153 | GGCATGGGTTAAAGT[A/G]CTCTGTAACATGTAA | 57630 |
| rs114490346 | snp | C/T | 0.159622 | 0.233092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192825 | TATATATGTGATATA[C/T]ATATCATATAGATGT | 57630 |
| rs114499396 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184463 | GCATCCAGGTGGCTT[C/T]ACTTCATTGCAAGCT | 57630 |
| rs114501310 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229729 | CAGCTTACTCATCAC[A/C]ACTGGGAACAAAACC | 57630 |
| rs114504131 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102408 | AGATTTTTTTTTTTC[C/T]CCCAATTTAGGAGAT | 57630 |
| rs114510940 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148578 | ATAAAATCATTAAAA[A/G]TATCCTTTACATAAG | 57630 |
| rs114525742 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238140 | TGCCTCCTACTGTAA[C/T]ACTCTAATGCAATAT | 57630 |
| rs114535034 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232194 | TCAGACCCAACAGGC[A/T]CTTGGAGACAGTGCC | 57630 |
| rs114553300 | snp | C/T | 0.029116 | 0.117091 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215226 | CATATAGTTTTTCTT[C/T]TTTAGTTTGTTGCTG | 57630 |
| rs114595139 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250492 | ATTCTCCTATTTGCA[A/T]TATTTTTCAACATGA | 57630 |
| rs114604230 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105675 | GGGGCAGGAGAATGG[C/T]TTGAGTTCAGGAGTT | 57630 |
| rs114640140 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249575 | ATATAAGGGTATTCT[C/T]TAATTCTATGTGGAA | 57630 |
| rs114654910 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258208 | GAAAGCAGGTCTCCT[A/C]ATTCTTTCCACCATA | 57630 |
| rs114713200 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225254 | AGTATGACCTGCTTC[A/G]GCTTCAGACATATTA | 57630 |
| rs114731121 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113422 | GCCCCAATTTTCAAA[A/C]ACATGACACCAAAGC | 57630 |
| rs114816440 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245842 | GGCAACAGGGGAGTA[A/T]CCGTACAAGACCACC | 57630 |
| rs114847487 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103873 | CCCCTTTCCCACTTG[C/T]AAAAATTTAAATGGT | 57630 |
| rs114853701 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149299 | AAACAGCCGTTCCTG[G/T]AGCTCAGAGGAGACC | 57630 |
| rs114876653 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098152 | ATGCTTATTATTGTT[C/T]TAAGCCACTGACTTT | 57630 |
| rs114927689 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262360 | AAATCTACATTCTTT[C/T]TCATTTTAAAAATGA | 57630 |
| rs114927810 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100663 | AATATTCTTAAGTGG[C/T]AACTCTATTTGCAGC | 57630 |
| rs114928344 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235970 | ATAGGCGTGAGCCAC[C/T]GTGCCTGGCCTACTT | 57630 |
| rs114936590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193192 | AGCTCAGTGCATACT[A/G]CCCAAGTGATGGGTG | 57630 |
| rs115030333 | snp | A/T | 0.208474 | 0.246527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229933 | ATGCTTGGCCAGGCG[A/T]GGTGGCTCATGCCTG | 57630 |
| rs115034822 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143123 | TGTCTCTTAGAACTA[C/T]CAAGGGAAGGAAGTG | 57630 |
| rs115035753 | snp | A/C | 0.00166344 | 0.0287915 | missense | SH3RF1 | GRCh38.p7 | 4:169269037 | GGAAGCTCCTCGACA[A/C]CCGAGCCAACAAGAG | 57630 |
| rs115118234 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240439 | CTGGGCTCAAGCAAT[C/T]GACCTACCTCAGCCT | 57630 |
| rs115141819 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105295 | TATAAGATATAAAAA[G/T]AGTCCACTATTTTGA | 57630 |
| rs115153544 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267932 | TCTTACAAAAATGAA[A/G]TTGTTTTAATTACTG | 57630 |
| rs115187539 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209371 | GTTCTCAGATAAGGA[G/T]CCACTTCATCCGGGA | 57630 |
| rs115188127 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111583 | ATCTTTTTATAACAA[C/T]AAAACACAATAAAAC | 57630 |
| rs115189411 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260345 | ATGGAGAAGGACTGC[C/T]TTCCTGCTCCCCCTG | 57630 |
| rs115191456 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160545 | GCTAAAATTGTTTCA[A/G]TGATCAATAACCACA | 57630 |
| rs115195887 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213043 | GTTTTCGACTAACTT[A/T]GGCAAACACCAAGCA | 57630 |
| rs115234773 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198290 | CTGGCACAATGAATA[C/T]TTTTAACATCCCCAG | 57630 |
| rs115239558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182326 | CACAAAGGAGGGTGA[C/T]CCAAAAATCACTGAG | 57630 |
| rs115308667 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099078 | AGATCAACACAGTTA[C/G]GGTTTTGGAATCCCT | 57630 |
| rs115311105 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143996 | CCCTGAACTTCACAC[C/T]GAAAGGTTTAGGTTA | 57630 |
| rs115315149 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129430 | TATCTCCTGGCTACC[C/T]TAATTCTCCCTATTA | 57630 |
| rs115316796 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152781 | AGTCACTGTACCACC[A/G]TCGCTATTTTATCAC | 57630 |
| rs115317896 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171361 | GTTGAGTTTGTTTCT[C/G]TTTTAACACACCCAA | 57630 |
| rs115380194 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199039 | TTGTAAGAAGGAAAA[A/G]GAAGCAAATAAATTG | 57630 |
| rs115396377 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225285 | GGTTTGAATGCTGGC[C/G]AACTTCACAGGTAGG | 57630 |
| rs115401496 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176965 | TAAAGACAGGGTTTC[A/G]CTATGTTGCCCGGGT | 57630 |
| rs115432766 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157087 | ACTGAGGAGAAATGA[C/T]AGATACTGAGGGGAA | 57630 |
| rs115447922 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158167 | AATGATAAAGATATG[C/T]ACACCATTTATGGGG | 57630 |
| rs115466424 | snp | A/G | 0.0248432 | 0.108648 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096182 | GTATCTATTATACGA[A/G]AAGTTCAAGTTTAAA | 57630 |
| rs115469794 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237878 | TTATGATTTCCCCCC[C/T]GCTCCACACCCTTGA | 57630 |
| rs115480041 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179793 | TTACTTTGAATAAAT[G/T]TTGCAGTGCTCTACT | 57630 |
| rs115491430 | snp | C/G/T | 0.0201874 | 0.0986251 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139751 | CCTGGAGTGGTGTAA[C/G/T]AAGCCAACTGGCAAG | 57630 |
| rs115572762 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134737 | GATATGATTAGTTAA[A/C]TGTAAAATGACATGG | 57630 |
| rs115574930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163964 | TCTTGTGTGGGTCAA[C/T]AGGACAGTCTCTATT | 57630 |
| rs115578411 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125434 | CCTTTCATGCAACCC[A/G]CCCAGGTAGTGATTG | 57630 |
| rs115646064 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164994 | AGTTTGTGTCACTCA[C/T]TGCCTTGAATATTAG | 57630 |
| rs115648639 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132687 | TAAGGTGGGGAAGAG[C/T]TGGGGTAAGCAAAAA | 57630 |
| rs115651394 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195515 | CTATTCAAATACTGC[A/G]GTGCTCCACTTTAGT | 57630 |
| rs115655858 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127939 | TAAAATATTTACTTC[A/G]CCAGTTAAGCATCCC | 57630 |
| rs115701127 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167214 | AAGATGTTTGTATAG[C/T]CATGGAAGGGCACTC | 57630 |
| rs115753026 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223550 | AACATATGGTCCCAG[A/T]TGTGGGGGATACACC | 57630 |
| rs115754399 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199514 | AAAGCCTTGGCCCCA[A/G]CATGGTAAAAGTCAC | 57630 |
| rs115766579 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123629 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57630 |
| rs115793406 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115956 | GGAAATTCCTCCACG[A/C]GACTGTAAGCTGCAC | 57630 |
| rs115800571 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262802 | ATTATCAATTAGTAT[A/G]CACCACAGACCCCCT | 57630 |
| rs115802391 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253335 | CTTAGTCTCCTGAGA[A/G]AAGTAATAACTCAAG | 57630 |
| rs115822074 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097693 | AGCCAACCTCCAAGA[C/T]GGCCCTAGTGATCCT | 57630 |
| rs115866392 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215115 | AAATTTTTTTTCTTA[C/T]CAAGTTGAGGTAGTC | 57630 |
| rs115873145 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229727 | CACAGCTTACTCATC[A/G]CAACTGGGAACAAAA | 57630 |
| rs115873468 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147680 | AAAGCAATGTTGTTT[C/T]ATAACACTTAGGAAA | 57630 |
| rs115887677 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225545 | TGTAAAGGAGGGTAA[A/G]CTGGGTAAAAGGCCA | 57630 |
| rs115892955 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141289 | AAAACCAAGCAATCC[A/G]TTCTATTCTCTCATG | 57630 |
| rs115893122 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124610 | GTGCATGCATGTTTG[C/G]ATGTGTAAATTTGTG | 57630 |
| rs115932847 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162152 | ATAGAGTGAGACTCC[A/G]TCTCAGAAAAAAAAG | 57630 |
| rs115939006 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237251 | ACACGGTGAAGGTGA[C/T]TTGAAAGTCATACTT | 57630 |
| rs115968771 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218140 | GTGTAATATATATTA[C/T]TATATATTGATTATA | 57630 |
| rs115983637 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201852 | AGAAAACCCATCTGT[C/T]GTCGCTACAGAGGCA | 57630 |
| rs115991914 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168973 | AAATCAAGCCAGCTT[C/T]AATACTCCAAAGTCT | 57630 |
| rs116005626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108910 | GGAAGGAAGGAAAAA[C/T]ATAGCTAGTGCCAGG | 57630 |
| rs116011793 | snp | C/G | 0.145978 | 0.227331 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219988 | CTAGCGTGTGGTACT[C/G]TAAATTACAGGAAAG | 57630 |
| rs116049376 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185084 | TAATAGGAGTGTCAA[G/T]ATTTCCTTCCCTATA | 57630 |
| rs116052521 | snp | G/T | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228517 | GAGTTCCTCATCACA[G/T]AACATCACTCGGACC | 57630 |
| rs116091561 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252404 | AATATTCCATAGGAT[C/G]AGCTTTTAAAATGTT | 57630 |
| rs116113995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119506 | TAAAAATGTTTTCCT[G/T]CATTAACTTTATTTT | 57630 |
| rs116116532 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198762 | GAAGACTTTACAAGA[C/G]AAAAAAGAGAATCTA | 57630 |
| rs116146634 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234567 | GGTGAGAATTAATTA[A/G]CAAACTTCTAACACT | 57630 |
| rs116146701 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105139 | GTAAGATTTCAAGTC[A/G]GCAACATAGAAAATG | 57630 |
| rs116173565 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123304 | ATCTGGCTGTTAATA[C/T]AGACATACATAGTTC | 57630 |
| rs116208849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096762 | TACTGTTAGTCTGCA[C/T]GAACCTTCAACATAA | 57630 |
| rs116259402 | snp | A/C | 0.00597247 | 0.0543191 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094982 | GGTAAGGATCTTATT[A/C]ATTACCAGGCTGTCT | 57630 |
| rs116289338 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191030 | TCCAGCATCCCTTTA[C/T]GATTAAAACTCTGGG | 57630 |
| rs116290712 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097488 | GGCAGAAGCTTAGTT[A/G]GTTTAATATTATCTG | 57630 |
| rs116291315 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231624 | TAAATTTCTCCTACA[C/T]TCAAGATTCTAAATA | 57630 |
| rs116308829 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244792 | TTAGTGTTTTTTGCC[A/G]TTGTTATAACCTGTT | 57630 |
| rs116313860 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158908 | ATATTAATTATTGCT[C/T]TCAAAATGCTATTGG | 57630 |
| rs116340306 | snp | G/T | 0.0103418 | 0.0711614 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134722 | TCTTTTTCTCACACG[G/T]ATATGATTAGTTAAA | 57630 |
| rs116340810 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169076 | ATCTTCTTATTTTTG[C/G]TGTTGAGAGTAATAC | 57630 |
| rs116348375 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257641 | CTGAGAAAAGAAATA[C/T]GGTTAGGTAATTCTA | 57630 |
| rs116349993 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211727 | GATGTGTGAATGTAT[A/G]TGTGTGGTTTATGGA | 57630 |
| rs116350283 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127178 | AGTATTGCTCATAAT[G/T]TTGGATATTTAAAAT | 57630 |
| rs116366000 | snp | A/C | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228519 | GTTCCTCATCACATA[A/C]CATCACTCGGACCTT | 57630 |
| rs116375217 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150416 | TGATGTTTTAAAATA[C/T]GTATACACTGTGGAA | 57630 |
| rs116389182 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265061 | GCAGGTCTTTCTTCT[A/G]TCCTCTCCCCTAGCT | 57630 |
| rs116404474 | snp | A/T | 0.0547245 | 0.156101 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247516 | TCCAGACTACCATGA[A/T]CTGTGTCTGAGAGTC | 57630 |
| rs116412876 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145031 | TGAAAAAGGCAAAGA[A/G]TTTCAGAGAGATTAA | 57630 |
| rs116427500 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117195 | AGCACACCCGTTAGT[A/T]GAGTATCACGCAATG | 57630 |
| rs116431539 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104006 | AAATGCCATCACCTG[C/T]CTGAGCTAGCAATTC | 57630 |
| rs116509229 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225524 | CAAGAGGGTTAAAAG[A/C]ACAGATGTAAAGGAG | 57630 |
| rs116599133 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188717 | TTTCAACCTGTATAC[A/G]GCAGTTCAATAAATT | 57630 |
| rs116604760 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097005 | TTCATTTCATTTCCC[A/G]AGAGGGGTATCATTT | 57630 |
| rs116631825 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105641 | GCTCACGCCTGTAAT[C/T]GCAGCATTTTGGGAG | 57630 |
| rs116651866 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213107 | TTTTGTAAGAGACTG[C/T]CAAATTGTCTTCCAA | 57630 |
| rs116661023 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260410 | GCCACTTGGAAAGAA[C/G]AGACCACAGTTGCAG | 57630 |
| rs116686989 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141590 | TTTCCATACTCTATC[C/T]ATATTTCTATTGGAT | 57630 |
| rs116723564 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161162 | AAGCCAAAGAGAAAC[C/T]GACTCTGCAGTCTAA | 57630 |
| rs116734530 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264185 | CAGTTCTGGAGGCTG[G/T]AAGTCCAAGATCAAG | 57630 |
| rs116740420 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162322 | CTCAAGATATCTACA[A/T]CAGATAATCACTCAA | 57630 |
| rs116827644 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188207 | TTTGGTAATTTGTTA[C/T]AGCACCCCTAGGAAA | 57630 |
| rs117012703 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193963 | TTCTCAGCTGTACTA[A/C]GACAATCTCAAGGAT | 57630 |
| rs117015368 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101102 | TTACCATCTGTGTCC[A/G]TCTCGTTTATTCTAC | 57630 |
| rs117047039 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230176 | GCTGCTCCAGCCTGG[A/G]CCACTAAATGAGACT | 57630 |
| rs117123818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244645 | TAACCAAAATGTAGG[C/T]AGAAAGAGTTAACCT | 57630 |
| rs117151673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144573 | AAAGAAAACCTAAGA[A/G]ACAGCATGATGGATT | 57630 |
| rs117166768 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254164 | CTTACAAGGATGTGA[A/G]TGTGTTCCGATGGAC | 57630 |
| rs117169530 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107328 | TTTTGTGGGTCCATA[A/G]TAGGTATATGGGGCC | 57630 |
| rs117181616 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132064 | GTGTACTTTCATTTT[G/T]AACAAATCTCTGCTT | 57630 |
| rs117220488 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210197 | ACTCCATCTGGAGTC[C/T]TTCTGCTATTTTACC | 57630 |
| rs117221816 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133973 | AGCCATTTCCCCATA[C/T]GCACTGATCTCCATG | 57630 |
| rs117291048 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229842 | CTACAATTAAAATCT[A/G]CTTGAAACAACACAA | 57630 |
| rs117330804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234598 | GGACTTGCCATTTAA[C/T]AGACTTTGCTATACC | 57630 |
| rs117436542 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184430 | ACATGGGCTGTGAAG[A/T]CAGTCAGACCCGGGC | 57630 |
| rs117495629 | snp | A/G | 0.000263696 | 0.0114795 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169269042 | CTCCTCGACACCCGA[A/G]CCAACAAGAGTCCTG | 57630 |
| rs117587744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170635 | TCATATCCTGGGGGC[A/G]CAACACACAGCAAAG | 57630 |
| rs117618103 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270030 | ACCAAAAGAATTCGA[C/T]AATGGAAGGTTGGAC | 57630 |
| rs117715120 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112154 | TAAGTAAATGGATGA[C/T]GATGCTCACAAAATG | 57630 |
| rs117759530 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213382 | GTTCATTTTCTTACT[A/G]TTGAGTTTTAACAGT | 57630 |
| rs117829677 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141342 | TTGCATATCAATAGG[A/G]ATAGGCTGATAGCAT | 57630 |
| rs118178415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118425 | AATTGTTTATGCTTT[A/G]GCCCTTGATTACAAA | 57630 |
| rs118191807 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253720 | AAAGAAGCCATTATA[C/T]ATGTAACATTTTGCA | 57630 |
| rs137871454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217132 | CATGCTATTGCACTC[C/T]AGCTGGGTGACAAAG | 57630 |
| rs137893048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141145 | AAAGGCCTCAGCCAG[C/T]TCCCCACATCTGTCT | 57630 |
| rs137893388 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103721 | GATCTAAGAATCCAA[C/G]GTAAATAAATACTAT | 57630 |
| rs137903926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171282 | GACCACACAGCAGCA[C/T]CAGAGTTGCTCTGAA | 57630 |
| rs137911203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221963 | TCAAAGTAAGTCTTC[A/G]TTCCCCTCATCCATC | 57630 |
| rs137965884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207866 | TAAAGGGTCCTCACA[A/G]AAGCAAACCTCTCCC | 57630 |
| rs137970736 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175912 | TAATTAGGTTTGGTT[A/T]GTATGAGAGTGGAAC | 57630 |
| rs137974213 | in-del | -/TGTTGT | 0.157932 | 0.232429 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176927 | TGCCTGGTTAATTTC[-/TGTTGT]TGTTGTTGTTGTTGT | 57630 |
| rs137979366 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254578 | GGTAGTAAAAACTAA[C/T]CACTCGAGAGATGGG | 57630 |
| rs138002946 | in-del | -/A | 0.068335 | 0.171749 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107210 | TTTTTTTCTTTCTGG[-/A]AAAAAAAAATAATGA | 57630 |
| rs138018097 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165574 | CGTGCCTGTAGTCCA[A/G]TATTGTGCCACTGCA | 57630 |
| rs138067009 | snp | C/T | 0.000119545 | 0.00773033 | missense | SH3RF1 | GRCh38.p7 | 4:169117781 | AAGCATTTGTCACCG[C/T]CCTGCCAAGACACAA | 57630 |
| rs138068274 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201921 | CTGCAAGGACCTGTA[A/C]CAGGAGTCAGTGAAC | 57630 |
| rs138083790 | snp | C/T | 0.00288172 | 0.0378491 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120778 | AAAAGAACAAAGCTT[C/T]TCTGTTTAGAACATA | 57630 |
| rs138085813 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169529 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 57630 |
| rs138098567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134359 | TCAGGCATGCTCACA[C/T]CTGAATGCTGAGCTC | 57630 |
| rs138162973 | snp | A/G | 3.6616e-05 | 0.00427863 | missense | SH3RF1 | GRCh38.p7 | 4:169116607 | TCACTGCTGCCGTGG[A/G]GCGTTCCTGGTTGTG | 57630 |
| rs138167449 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197470 | GTCTCTACTAAAAAC[A/G]CAAAAATTAGCCAGT | 57630 |
| rs138180469 | in-del | -/CTT | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171910 | GAAAGGTTATATCTG[-/CTT]CTTCTCCATCCGCAC | 57630 |
| rs138239574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164595 | CTAGGCTGCTGGGAA[A/G]CCTGGGGCATGCTAA | 57630 |
| rs138267411 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147561 | TGACCATCAGGACTT[A/T]GCACGTTTGTTTGAG | 57630 |
| rs138289677 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151049 | ATGGGAGAATTAGCT[C/G]AAAAATGTAGAAGTT | 57630 |
| rs138352813 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156732 | ATGGTCTTAAAATGT[C/T]TCTGAAAATACAACT | 57630 |
| rs138364797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228337 | CAGTTCTGGAGGTCA[A/G]AGTACAAAATGGGTC | 57630 |
| rs138372683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100224 | AGGGGTCAATGAATA[C/T]TCTCCCATGACCTAC | 57630 |
| rs138377935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181645 | TCATGATGATGATAC[C/T]TGAGTGTGTAAAAAT | 57630 |
| rs138424148 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237863 | TCCTGCTAAATCAAT[G/T]TATGATTTCCCCCCC | 57630 |
| rs138454895 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100549 | GTTTCAATATATTGG[C/T]CAGGCTGGTCTCTAA | 57630 |
| rs138536928 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146916 | GATGAAAGGCCTAGG[C/G]AGAGAAGACAGCAAC | 57630 |
| rs138539671 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250254 | AAGGATTTGTATTCA[C/T]TTCTGGGAGCTAAAA | 57630 |
| rs138591454 | in-del | -/G | 0.0232847 | 0.105357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193593 | ATAGACATTTACCCC[-/G]TTACTAAGGATGCTA | 57630 |
| rs138608620 | snp | C/T | 4.9694e-05 | 0.00498443 | missense | SH3RF1 | GRCh38.p7 | 4:169117712 | TGGAAGGACTGACCA[C/T]GGTCACTCCCCGACT | 57630 |
| rs138614718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257202 | TTTCTGTCCAGCAGG[A/G]ATCACAGAGCACACA | 57630 |
| rs138618951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130797 | TTTACTAGAAAGAAA[C/T]TGAGTTATTCAGGTC | 57630 |
| rs138651269 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132349 | GGGATAAGTCCCTTC[A/G]TGTCTCTAGGCCCCT | 57630 |
| rs138665206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243928 | CAGATACTTTTACTT[A/G]AATAACTGCAAACAT | 57630 |
| rs138675771 | in-del | -/TTTG | 0.151668 | 0.229849 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107954 | ACAAATAAGCGTGTT[-/TTTG]TTTGTTTGTTTGTTT | 57630 |
| rs138698443 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134801 | TCATCCAACAAATAC[A/G]TGTTGAGTGCTTTCT | 57630 |
| rs138722723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213033 | AAAGACATAAGTTTT[C/T]GACTAACTTAGGCAA | 57630 |
| rs138722799 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261967 | ACAGAAAGAAAAATG[C/T]TATGAGAAAAATACT | 57630 |
| rs138734139 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162102 | GCAGAGGTTGCAGTG[A/C]GCCAAGATGGCGCCA | 57630 |
| rs138735697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157333 | ATCTGTAAGTGTATA[A/G]ACACGTGGTCTTTTA | 57630 |
| rs138761106 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216622 | GAGGTGGAAAAATCA[A/G]TTGAGCCCAGTGGTT | 57630 |
| rs138824007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125279 | TTGCTAGAGTGAGCA[C/T]CCAGGGAAGAAGTGT | 57630 |
| rs138884702 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104164 | GGAGGGAGGCTGCAG[G/T]GCCCATGCCAGTGCC | 57630 |
| rs138904365 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150683 | CATCTTAGGGCCCCA[C/T]GTCCGAGGAATGGAG | 57630 |
| rs138924214 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263028 | TTTTCCGTTTTAATT[C/T]AATCATTCTGAAACA | 57630 |
| rs138961315 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187263 | GAGCGCAGTGGTGTA[A/T]TCTTGGCTCATTGCA | 57630 |
| rs138994060 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191239 | AGTAGCTCTTCTATA[C/T]ACCAACAGCGACCCA | 57630 |
| rs138994220 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141607 | TATTTCTATTGGATT[A/G]TTAGTATTTTTCTTA | 57630 |
| rs138996640 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238312 | ACCTACCAGGTGTCA[C/T]GGGCATGGAAGGATG | 57630 |
| rs139013270 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265595 | TCTCCAGCCTTGGCC[C/T]CCTGAGTAGCTGGGG | 57630 |
| rs139035508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242901 | TTCTATCATTATAAA[C/T]CACCCAGCCTGTTAT | 57630 |
| rs139062074 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199426 | GGCTTCACCAACCAT[C/T]AGGGTCTTATAATCT | 57630 |
| rs139070494 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128224 | GAAGGAAAGGAGAGA[G/T]TCTCCCCTGGAGATG | 57630 |
| rs139091630 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115513 | AATGCCTGAGGATCT[C/G]TCACTGTCTGCCATC | 57630 |
| rs139165329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158981 | GTTAATTAGAACTTC[C/T]CTGAGAGGCCAATGT | 57630 |
| rs139167689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193279 | ATTCCCCAATAACCT[A/G]TGGAAATAGTGAATG | 57630 |
| rs139186743 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235829 | GGGATTACAGGTGTG[C/T]ACCACCAGGACTGGC | 57630 |
| rs139194288 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156707 | AGAGGGATGAATTTT[-/T]AATAAAATAATGGTC | 57630 |
| rs139200386 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148593 | ATATCCTTTACATAA[A/G]ATATGGCTCTAAGAA | 57630 |
| rs139232401 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230135 | GCTTGAACCCAGGGG[C/T]GGAGGCTGCAGTGAG | 57630 |
| rs139251398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101760 | TCCCTTTGAACAAAG[C/T]GCTGTGGAGGCATTA | 57630 |
| rs139260138 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120056 | GCCAGATTATGATTA[C/T]TTTTTGTGGGAGGCT | 57630 |
| rs139296355 | snp | C/T | 8.54898e-05 | 0.0065374 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117779 | GGAAGCATTTGTCAC[C/T]GCCCTGCCAAGACAC | 57630 |
| rs139338011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162856 | CCAAGGCCAGCCTTT[A/G]GGCTTTTTTAGCGCT | 57630 |
| rs139358685 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178071 | CATGGTGAAACCCTG[C/T]CTCTACTAAAAATAC | 57630 |
| rs139464384 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260025 | ATACTAGAGAGGGGA[G/T]AGATTAATAAATGGA | 57630 |
| rs139482224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159252 | TTCTAATTTTTCTCT[A/C]CCCTCACAGATGCCT | 57630 |
| rs139490019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167211 | AAGAAGATGTTTGTA[C/T]AGCCATGGAAGGGCA | 57630 |
| rs139496602 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165712 | AGTGTTTACATTAAC[A/G]CCTTGGAGAGAGGAT | 57630 |
| rs139505085 | snp | C/T | 0.306431 | 0.243548 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145965 | CTATATAAAATATTA[C/T]ATATTCTATATATTA | 57630 |
| rs139514068 | in-del | -/T | 0.133435 | 0.221162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206389 | ATCCATTCAAGGGGC[-/T]GGGGGAAGGGGGGTG | 57630 |
| rs139546524 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235368 | TAGCTAATACTCATT[C/G]AACATTTACTATATT | 57630 |
| rs139566971 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106288 | TATTTCTTTGTATTT[G/T]AGTAGAGACAGGGTT | 57630 |
| rs139583134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121454 | TAGAGGCTTGAGCTA[C/T]ACCTGCTTTTTATGC | 57630 |
| rs139584771 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138474 | CCATAAGCTTATTTA[A/G]ACACCTAGAAACAAA | 57630 |
| rs139608112 | in-del | -/TCAG | 0.0240643 | 0.107019 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220080 | CAAAATTGTTTCCAA[-/TCAG]TCAAAGTGAATCATC | 57630 |
| rs139608795 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263134 | CCATCCCCATCTGTG[A/C]GAAGACAACAACTCC | 57630 |
| rs139621686 | in-del | -/A | 0.135825 | 0.222405 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262682 | AAAAAATAAATAAAT[-/A]AAAATGATAACACTT | 57630 |
| rs139659041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223488 | AGAGCATGAGGCAGG[C/T]AGGGAAGAGACATCC | 57630 |
| rs139668450 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270667 | GCAGCTTCCTGCCCG[G/T]AGAAGGCAGAGGCCG | 57630 |
| rs139685286 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095479 | TAATACATGCAAGAC[A/G]TGGGGAAAGAATCAC | 57630 |
| rs139690961 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143284 | AGCCCAATGTATCTA[C/T]ACTATGATCACTTCA | 57630 |
| rs139719273 | in-del | -/AA | 0.0162398 | 0.0886349 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246125 | GTGTCTGAAGTTGGC[-/AA]AGTCATTCATGCAAA | 57630 |
| rs139721224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142105 | TTACAGGTGTGAGCC[A/G]CTGCACCTGGCCTTA | 57630 |
| rs139730155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102413 | TTTTTTTTTCCCCCA[A/G]TTTAGGAGATGAGCT | 57630 |
| rs139737191 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096302 | TCAGACAGTACAAGG[C/G]ACACCTTATACATCC | 57630 |
| rs139738010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184197 | GAAATCCATTTGGTA[C/T]GGCAGGAGATCTCTT | 57630 |
| rs139758058 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231025 | TAACGAAAAGGCCAC[C/T]GGTGCTAGGGCATAG | 57630 |
| rs139768997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224279 | TATAAACAGAGGAAA[C/T]GGCATATTGCCTATT | 57630 |
| rs139795296 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234367 | CAAGAGTGTGAGGTT[A/G]GGAAACCCTGATTTA | 57630 |
| rs139850941 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198665 | TAAGTATATTAAGCA[A/G]AACGATTACTAAAGA | 57630 |
| rs139861160 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247324 | TCTTCCCCCAAATAA[A/G]TATTTACTGAGAGAG | 57630 |
| rs139903414 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148415 | TTAGTAGTACTACAA[G/T]TATATGGCGAGAGGC | 57630 |
| rs139926739 | snp | C/T | 3.36005e-05 | 0.00409867 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106993 | GGCTGCTCCTGCCAC[C/T]GCAGTCGTGACCGGT | 57630 |
| rs139952820 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171667 | TATTTTTGAACACCC[C/T]AAATCTCAGAAACTT | 57630 |
| rs139961007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203988 | CTACTATGAAGAAAG[C/T]GCCTGGCATAATCTT | 57630 |
| rs139982521 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217584 | CCTGAAAGGTGTACA[A/G]GACAAGTTACTAAAC | 57630 |
| rs140088542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259333 | TTTCATGTTTCACAA[C/T]GCAAATAATCTACTA | 57630 |
| rs140125414 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118602 | CTGGGAGTACAGGCA[C/T]GCGCCACCATGCCCG | 57630 |
| rs140126837 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137331 | AAAAGCCCCAGTGTA[A/G]ATTAAGAGTACCAGG | 57630 |
| rs140146369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133252 | TGAATACTAACATTT[G/T]TAAGCCCCTTACTTT | 57630 |
| rs140146462 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183342 | CTGGAGTTCAATGGC[A/G]TGATCCTGGCTCACT | 57630 |
| rs140159415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163362 | AATACATTTGTCCCA[C/T]CTCCTGGATTTTCCT | 57630 |
| rs140171351 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140632 | AATAAAAACAACAAG[G/T]CAGCTTAAGAAATAT | 57630 |
| rs140173693 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264681 | GCTAATCGTCTCAGT[A/C]CCAATGGTCCCTCTT | 57630 |
| rs140181893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210704 | AAGACTGTAAACTAC[A/C]CTTGTGTCAATCACT | 57630 |
| rs140207710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232404 | CATAACTCTGTGTGG[C/T]GTGACAACTGTTATT | 57630 |
| rs140209433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186288 | TCTGTATAACAAACC[C/T]CATGACACATGTTTA | 57630 |
| rs140258776 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209086 | TTGAGGTCAGAAGTT[C/G]GAGACCAGCCTGGCC | 57630 |
| rs140290759 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152465 | AGATGTGGCTGGGTG[C/T]GGTGGCTCACGCTTG | 57630 |
| rs140291823 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103407 | TTACCAAAGGAACCC[G/T]GGGCTCCTTCTGCAT | 57630 |
| rs140292688 | snp | C/T | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169156654 | TAGTTGTATAATGCT[C/T]TGGCACATGGTAACT | 57630 |
| rs140326402 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128756 | GGTCCTAAGCACTCT[A/C]GCAGAGGGAAATAAA | 57630 |
| rs140373899 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133708 | CTTGAACCCAGGAGA[C/T]GGAGGTTGCAGTGAG | 57630 |
| rs140384139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260206 | TACTGCCCCTACTCA[C/T]ATGCCTTTTTTGAGC | 57630 |
| rs140399489 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249305 | TGATAAAGCCCCTTA[C/T]AAAAGAGGCTTCACC | 57630 |
| rs140425882 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215105 | GATTTGGGGTAAATT[A/T]TTTTTCTTATCAAGT | 57630 |
| rs140460248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211640 | CAATTCAAATGAAGG[C/T]CTGCGTGCTTCTAGA | 57630 |
| rs140483998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168608 | TACAGGCTTAAACTC[A/G]TGCATGCATTATTTA | 57630 |
| rs140507335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251863 | TTAACCTCTATTTTA[C/T]TAACAAAACTGTGAT | 57630 |
| rs140545290 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129004 | GAGGCTTAAAGAGGC[-/A]AGAGTACCTTTTCCA | 57630 |
| rs140551094 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130681 | CAGCTGCCTAGACAT[A/G]CTTAGAGCGGGCAAT | 57630 |
| rs140569486 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124225 | AAGGCAGAAAACTAA[C/T]GGCATGTGCTCAAAC | 57630 |
| rs140575956 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236623 | TGCTATGAGAATTAA[A/C]TAAGTTAATATACAT | 57630 |
| rs140576349 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144354 | TACCTATTCTCAACC[A/C]AAACAAAAATATCCC | 57630 |
| rs140603551 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214561 | AGCCTTCCTATCCAT[C/G]AATGTGGATTATCTC | 57630 |
| rs140611920 | in-del | -/ACAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168216 | AATGGCAAAATGAGA[-/ACAA]AAAGAAATCTGAAAT | 57630 |
| rs140617109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189359 | ATCTGGTATTCTATT[C/T]TGACCAGTCCCACAT | 57630 |
| rs140619010 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191775 | TTCGACAAGGCAAAC[A/G]AAAACAAAGTGGGGG | 57630 |
| rs140658147 | in-del | -/TA | 0.0584853 | 0.160693 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222511 | ATTTTTATACATATT[-/TA]TATATATATATATAA | 57630 |
| rs140738748 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105437 | CCTAGAACCCCAGTG[G/T]GGTATCAAACAGAAC | 57630 |
| rs140749722 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188397 | TCACTCTCACTGTAA[A/G]CAATAGTGTCCACAA | 57630 |
| rs140758406 | snp | C/T | 0.000106878 | 0.0073094 | missense | SH3RF1 | GRCh38.p7 | 4:169116580 | CGGCGGCATTCTGTA[C/T]CTGGATGGGTGTCAC | 57630 |
| rs140761038 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099142 | TTGTTGCCCAGGCTG[G/T]TGTGCAGTGATGCAA | 57630 |
| rs140768319 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227628 | TTCCATAACATCTAT[A/G]CATTATTTATTTTAC | 57630 |
| rs140775945 | snp | C/T | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169156532 | TGGTGGGGAAAAAGC[C/T]ATGGATTCCATTGAC | 57630 |
| rs140836070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108379 | AATCTAAATCCCTAA[A/C]AACATTGTTCCATTA | 57630 |
| rs140847982 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191185 | GGATGCCCACCGTCA[C/T]CACTCCTCTTCAACA | 57630 |
| rs140870117 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173504 | AAAACAAGATATAAA[C/T]TGTCACTACAATCAT | 57630 |
| rs140875400 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220931 | AAGATCAGGCACAGG[C/T]TAAATTTGCCTTCAA | 57630 |
| rs140912457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194281 | TCACAAAGGGAAACA[A/C]TCATGGAACAACCAC | 57630 |
| rs140948213 | in-del | -/AAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166520 | AGGTTGAAAAGAAAA[-/AAG]AGGAGAAAGTTCTTG | 57630 |
| rs140989132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123493 | AAATGAGGTGCAGAG[C/T]CACTTACAAAGTGCA | 57630 |
| rs141009884 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251512 | TTAAACAGGCTATCC[A/G]AAAAACAGAAGCATA | 57630 |
| rs141070450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196106 | AGGAGTGAGCCACCA[C/T]GCCCAGCGAACACAA | 57630 |
| rs141082795 | snp | A/G | 1.74989e-05 | 0.00295789 | missense | SH3RF1 | GRCh38.p7 | 4:169136404 | TGATGAGGACAGGGG[A/G]GCTGATCTCCATGGA | 57630 |
| rs141091356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252732 | ACAGAGAATAAATAC[A/G]TGCTGATGGACTGAC | 57630 |
| rs141099365 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206125 | AGGATTTTAGAACAG[C/T]GGTGCTAAAGAGCAT | 57630 |
| rs141128542 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255665 | CACACACACACACAG[A/G]GTCCAGATAGATCAA | 57630 |
| rs141168712 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262288 | CACACTTAATAACAT[A/G]TTCTTCTATATGGTT | 57630 |
| rs141194541 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170813 | TTTACCATCAGAGCA[C/T]GTGTCTCATCTGGAA | 57630 |
| rs141208805 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254527 | GCCAATTGCTGACAC[C/T]ATCGTAAAGATTACA | 57630 |
| rs141245674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221556 | AACATTAACATTGGA[A/G]AAGAAAGTTCAATCA | 57630 |
| rs141262043 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169344 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 57630 |
| rs141280594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239214 | TGCCAAGATTGTGCC[A/G]ACAAGACTGGTTATA | 57630 |
| rs141282164 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130274 | GTACTTTCTGTTATT[C/T]GGGGAAGGTAGAATC | 57630 |
| rs141285371 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226910 | AGTGGCTTATGCCTG[C/T]AATCCCAGCACTTTG | 57630 |
| rs141290779 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126926 | TGCAATCTGTTTATA[A/G]ATTGGCCATGAGTGG | 57630 |
| rs141302172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172603 | GGAGATGTGTATGGG[A/G]CTAAGTTGACAAGGG | 57630 |
| rs141406554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233124 | CGTGGTGGCAGGCAC[C/T]TCTAATTCCAGCTAC | 57630 |
| rs141439168 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242982 | CTAGGTGTTTCTAAT[C/G]CAGGTGGTCCTTGGA | 57630 |
| rs141441174 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161090 | ATCCACAGAGCTTAC[A/G]TTTCACTTGGAGACT | 57630 |
| rs141444808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236074 | TTGCCATGTGTTTTC[C/T]GACAGTTCTAGCCAC | 57630 |
| rs141448257 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181128 | AGTGAGCCGTGCTGA[A/T]AATAATAGCCTTTCT | 57630 |
| rs141474253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116110 | GCGTTTCTTCCCCAC[C/T]CTACTCCTAGCACCT | 57630 |
| rs141478293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148259 | GGGAAGCGATGAACT[A/G]CAGAGTGGAGGCCAC | 57630 |
| rs141563359 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095172 | GCCTTCCAGAGCTCC[A/G]CAGTCACAGGAGTAG | 57630 |
| rs141563402 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222478 | CTAAAAAATACATAT[A/G]TATGTATTTTATATA | 57630 |
| rs141568676 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177668 | GTGTTAACTGTCTGA[C/T]CTACTAATTTAAAAT | 57630 |
| rs141571299 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100331 | ATGACTTCATTACCT[C/T]CCACCTCGTCAAATA | 57630 |
| rs141580642 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110115 | CACAGTGGCTTACAC[C/T]TGTAATCCCAGCACT | 57630 |
| rs141626503 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202644 | AGAAACCAAAGCATC[A/C]GTTAATTCCAAGCCT | 57630 |
| rs141631211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200694 | ACTACGTGCTCCCTT[C/T]ACCATTTAAAAATCT | 57630 |
| rs141684476 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154198 | GTTGTTTGGTTTTTT[-/T]CTGTTGTTTGCTTTC | 57630 |
| rs141688897 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212838 | GTGTTCAAAAAAATC[A/C]TGCGTGCTCAACTTA | 57630 |
| rs141692036 | snp | A/G | 0.00558655 | 0.0525553 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211498 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAGAAACTA | 57630 |
| rs141697311 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207673 | CTGGATGCTTCGAGC[A/T]TTGCTATGAAGATAA | 57630 |
| rs141713675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198209 | TTCCATAATCACAAA[C/T]TGGTTTTCAGGTTAC | 57630 |
| rs141736035 | snp | G/T | 0.00155792 | 0.0278663 | missense | SH3RF1 | GRCh38.p7 | 4:169116460 | GGGCACTGGCTCGAC[G/T]GATACTGATGGCAGC | 57630 |
| rs141769951 | snp | A/C | 0.000280193 | 0.0118329 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169269039 | AAGCTCCTCGACACC[A/C]GAGCCAACAAGAGTC | 57630 |
| rs141781469 | snp | C/T | 3.36242e-05 | 0.00410012 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106999 | TCCTGCCACTGCAGT[C/T]GTGACCGGTCCGTCC | 57630 |
| rs141797976 | in-del | -/AT/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192922 | TCATATATATGTGAT[-/AT/TA]ATATATATATATGAT | 57630 |
| rs141799475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155038 | TGACTTATTTAACAA[A/G]TATTTATTGAAGCCC | 57630 |
| rs141814650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201566 | TGCTAAGTGTGTTCA[C/T]CTCAAATCTAAAAGC | 57630 |
| rs141829325 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164972 | GTCACTCAAGTAAAA[C/T]GCAAGAAGTTTGTGT | 57630 |
| rs141862795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120702 | CATGGATTTTTAAAA[C/T]CTTGGCTATGTAACA | 57630 |
| rs141865392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159611 | GATTTAGTGAATTCA[C/T]ATATATAAGCCACAC | 57630 |
| rs141868581 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162145 | CTGGGCAATAGAGTG[A/G]GACTCCGTCTCAGAA | 57630 |
| rs141876403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268469 | ACATACATGTAATTA[C/T]GACTCTGAGCCCCAT | 57630 |
| rs141885272 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142508 | TCTTTTTACATCTCC[A/G]TCTGTGAACCATATG | 57630 |
| rs141903561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187942 | AAATCCAATGCCTGA[C/T]GAAGGCCATGTGAAA | 57630 |
| rs141964982 | in-del | -/GTG | 0.147321 | 0.227941 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219980 | AGTACAAACTAGCGT[-/GTG]GTACTCTAAATTACA | 57630 |
| rs141988697 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262633 | GATCTCACCATCGCC[C/T]TCCAGCCTGGGTGAC | 57630 |
| rs141998852 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136212 | AAAGTTACTATCTTC[A/G]GAAGTTCAAAATAAG | 57630 |
| rs142014032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217232 | TATAGTCAGACAAGG[C/T]TTGGTTCAACACCCT | 57630 |
| rs142038811 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163064 | CCTTGCTGTTTTGCG[A/G]GGGGCATTAATGGTT | 57630 |
| rs142042214 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181483 | GGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCAT | 57630 |
| rs142043438 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263077 | ATCCAAACCACCACA[A/T]TAAATGTCTTGCTTG | 57630 |
| rs142076175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261115 | CCCACAACCACTCTG[C/T]ATGGAGCTTAGGTCC | 57630 |
| rs142079487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247660 | GAAGACAATAAAGGG[G/T]TTGTGGATCTTGCGA | 57630 |
| rs142095087 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232021 | CCACTGAAGGGAGAG[A/G]GCACCAGGCCAGGTT | 57630 |
| rs142095321 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187593 | CAACTTTTTAAGCTT[A/C]TTCCCTTTTTCACTA | 57630 |
| rs142100181 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140980 | GAGGTTTTGTTTTTT[-/C]TTTTCTTTTTTTTTT | 57630 |
| rs142125396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118490 | TTTTTGAGACAGAGT[C/T]TCACTGTTGCCCAGG | 57630 |
| rs142185140 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265866 | AAATCATTGGAACTG[C/T]GCATAAAAAGCAGAA | 57630 |
| rs142209914 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134670 | CCTTTCTGGATTAAC[C/G]TCACTTTGCCCTTCC | 57630 |
| rs142212001 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185147 | TTCATTTTGTTCAAT[C/T]ATCCCACAAATATTT | 57630 |
| rs142218653 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181059 | TGAAATGTAGCCTAA[C/T]CCAGACACAGAAAAA | 57630 |
| rs142220920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264101 | TACAGTCAGAGTACA[A/T]GTTGGCTAGGGCTAC | 57630 |
| rs142222321 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147039 | AAATACCTATTACTT[C/T]TGGAGCAACAGATGT | 57630 |
| rs142229926 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111249 | GAGGCTGCAGTGAGT[C/T]GAGATCACACCACTG | 57630 |
| rs142233852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193023 | ATTATTCTAAGTGAA[A/G]TAACTCAGGAATGAA | 57630 |
| rs142260027 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141799 | AGTGCCACCATGGCC[C/G]GCCTAATTTTTGCTT | 57630 |
| rs142322524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101475 | GGAATGAAGAGTTAG[C/T]GCTTAATGAGTACAG | 57630 |
| rs142382221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168187 | TGAGTAACAAGCCAC[A/G]CTGGCTTTCAAGAGA | 57630 |
| rs142409162 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160202 | GATTTAGCACTCTTA[A/G]AAACCATTCTGAACT | 57630 |
| rs142461259 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245234 | ACTACTAACTGTGAA[C/G]TCAGAACTGGATGGA | 57630 |
| rs142488713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248502 | TGGGGTGGGAGGCAA[A/G]GAAAGGGAGAACATT | 57630 |
| rs142489684 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203221 | ACTCATAACTCAAAG[C/T]ATCTTGCTCTTTGTA | 57630 |
| rs142502481 | in-del | -/ATT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145947 | CATATTCTATATATT[-/ATT]CTATATAAAATATTA | 57630 |
| rs142541615 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272516 | GAGCAAATACATGGG[C/T]ATTTGAGCTGAGAAA | 57630 |
| rs142576818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114200 | CAGGGCTGGTTCCTT[C/T]TGGAGGCCACTGGGG | 57630 |
| rs142578844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163539 | TAGGACGAAAACCAG[C/T]AAACTATAACCACAG | 57630 |
| rs142580535 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191024 | ACAAAATCCAGCATC[C/G]CTTTACGATTAAAAC | 57630 |
| rs142605358 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250036 | TCAAGTCACGACACA[A/G]CCAAGATTAATAGGT | 57630 |
| rs142640738 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119532 | ATTTTTTTGTTCTTT[C/G]TTGCATTTCTCTTAT | 57630 |
| rs142641669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125336 | GAACACTGGCAGGTG[A/G]CAATGCTAGTGACAC | 57630 |
| rs142650569 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263703 | CATCATTACCTATCC[C/G]TTGAGTAATGCCTTA | 57630 |
| rs142675689 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183791 | AACAAAAAAAACTGG[-/A]AAAAAAAAAGTCAAC | 57630 |
| rs142676649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121287 | AGTTTCCAAGAGTGC[C/T]TAACTTGCTACCAGA | 57630 |
| rs142683019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139224 | TGGGATTACAGGCGT[A/G]AGCCACTGTGCCTGG | 57630 |
| rs142683744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202069 | GAGAATTAAATGAGA[A/G]ACAATGCTGTCAGCT | 57630 |
| rs142721028 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213090 | AGTAAGAGTATGTTT[C/T]GTTTTGTAAGAGACT | 57630 |
| rs142724989 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132718 | GGAGGTGGGGGTGGG[G/T]GTTTATTGCTTTCCC | 57630 |
| rs142753366 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133504 | AAAAAGAGGCTGTGC[A/G]TGGTGGCTCACACCT | 57630 |
| rs142758113 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135642 | TGGTATACACAGTGC[C/T]TAGAAGGGTCTAATA | 57630 |
| rs142784625 | snp | C/T | 0.000165739 | 0.00910175 | missense | SH3RF1 | GRCh38.p7 | 4:169116355 | GGAGTCCAGGGAGAA[C/T]GGTCACTATCCGGCC | 57630 |
| rs142790863 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260072 | AGTGGAAAAAAGCAG[C/G]CATTCTTCCCAATAG | 57630 |
| rs142798045 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196908 | ACATGTTAATCTCTA[-/T]TTTTTAAGTCTGTTA | 57630 |
| rs142900184 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129347 | TCTTTCTCTACTACC[A/G]AAGGTTGCATTTGCT | 57630 |
| rs142910108 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178189 | GAGTTTGCAGTGAGC[C/T]GAGATTGCGCCAGCA | 57630 |
| rs142921895 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255386 | ATATCTGTTTATATA[C/T]GTCACAATTTTTTTA | 57630 |
| rs142942030 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210805 | AGACAGTTGTTTCTG[C/T]ACCTCAGTTCCATTT | 57630 |
| rs142952694 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192774 | AGAAGCTGTTTCATA[C/T]ATATATACATATATG | 57630 |
| rs143001441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228634 | CCAGGTCAGCTGATT[A/G]GCAACCTTAACTCTT | 57630 |
| rs143021993 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222418 | TGCAGTGAACTGAGA[C/T]TGCACCACTACACTC | 57630 |
| rs143028977 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141478 | GTAAGTTTAAAAATC[A/G]TTTTTTGAAGTAACA | 57630 |
| rs143031757 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103899 | ATGGTTATACAAAAA[A/G]ACCTATCAAAGAATT | 57630 |
| rs143042623 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187187 | TATATAGTGTACACA[C/T]GTATATATGTATGTA | 57630 |
| rs143073245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102855 | CTATGAGATTGCTTA[A/T]GTCTTTATACCACGT | 57630 |
| rs143074323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100728 | ATGCCTGTGAGCAAG[A/G]TTAATCCTCAGCCTG | 57630 |
| rs143080627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182414 | TAATTAAGAATGCCA[A/G]TATATTTTTTCTTTT | 57630 |
| rs143089684 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150832 | AAATAACCAGTAGAG[A/G]TTACAAGATCTAAGC | 57630 |
| rs143128834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194286 | AAGGGAAACACTCAT[C/G]GAACAACCACCAGGA | 57630 |
| rs143129670 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196458 | ACTATATTTTTTATG[C/G]TGTGCTACTGCTTTT | 57630 |
| rs143134757 | in-del | -/CC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238972 | AATTTCCGCCCCCCC[-/CC]ACCCCTTGCCCTTTT | 57630 |
| rs143223047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206011 | ATTCATATTTTTAAC[C/T]GATAGTTTTAAATGG | 57630 |
| rs143282177 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255189 | TGTTCACCCAGTGTC[A/G]TTTCTTACCCAAAAC | 57630 |
| rs143297522 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149275 | ATTGAGTCTTTAGCC[A/G]TATTTATTAAACAGC | 57630 |
| rs143299406 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198722 | GACATATTATCATAA[A/C]ATTGCAGAACATCAA | 57630 |
| rs143307010 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160552 | TTGTTTCAATGATCA[A/G]TAACCACAAAGAATC | 57630 |
| rs143322875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257577 | CCCCGCTCTTTCAGC[A/G]TAATAAATGCCCTGT | 57630 |
| rs143326909 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158439 | AAGAATTACGGAACA[C/T]AAAGGAGAGGTAGGC | 57630 |
| rs143349455 | in-del | -/C | 0.159622 | 0.233092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198444 | ACTTTAAAATATACA[-/C]ATTTGTGAATGTCCA | 57630 |
| rs143365799 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124141 | ATATGGAGAAACTGT[-/A]AAATTACCACTTCAC | 57630 |
| rs143369728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265534 | ACTGGAGTGCAAGGG[C/T]GCGATCTCAGCTCAC | 57630 |
| rs143370600 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171306 | CTCTGAACCTATTAT[A/G]GTTGGGGGAACTGAA | 57630 |
| rs143421279 | snp | A/C | 3.40165e-05 | 0.00412397 | missense | SH3RF1 | GRCh38.p7 | 4:169116546 | TGATGGGACAGGCCC[A/C]CAGATGCAGGGCTGA | 57630 |
| rs143437686 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262511 | ACCTCTACTAAAAGT[A/G]CAAAAATTAGCCAGG | 57630 |
| rs143448312 | snp | C/T | 0.030278 | 0.119257 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181969 | ATTTGTCTCTCCCAC[C/T]GAAATGAAGAGAGAA | 57630 |
| rs143458772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254823 | GCAGGGGTTGGATAG[C/T]GTCCAAAGGAGAGTG | 57630 |
| rs143495196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257001 | TTACTGAGCATGTAC[C/T]AGGTCTTGGGCATTT | 57630 |
| rs143502164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132083 | AAATCTCTGCTTTTG[C/T]TGCTTCATTCTTTCC | 57630 |
| rs143531569 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130872 | TGCATAGCAGGTCCA[A/G]CTGCAGAATGCAGTG | 57630 |
| rs143541830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128487 | CAACATTATTAGCTT[C/T]CATTTAAATACAAGA | 57630 |
| rs143564612 | snp | A/G | 0.031825 | 0.122064 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212380 | ATTTTCTAATTTCTA[A/G]AAGATTCTCTGAAAT | 57630 |
| rs143567645 | in-del | -/AAACAAAC | 0.497091 | 0.0380279 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135174 | CCCCATCTCTATTAA[-/AAACAAAC]AAACAAACAAACAAA | 57630 |
| rs143638103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164343 | AGTGGAAAAAGAACA[C/T]ATCTAAAGGAAAAGC | 57630 |
| rs143658922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259541 | CAAAAGGATTGCAGA[A/G]CCACGAAAAAGGGTG | 57630 |
| rs143669622 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249121 | TAGTCCCAGCTACTC[A/G]GGAGGCTCAGGCAGG | 57630 |
| rs143682961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133331 | ACTACAAAAATTAGA[C/T]GGGTGTGGTGGCACA | 57630 |
| rs143700651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234386 | AACCCTGATTTAGAA[C/T]ATGATCTCAGACGAA | 57630 |
| rs143723147 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179025 | ATGGCCCCCAAAGTA[C/G]ACCACACCCCAATCC | 57630 |
| rs143724767 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120519 | TGTATCAACACTATG[C/T]CTTTTCTAGTAGAAA | 57630 |
| rs143752479 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138065 | CATAAAGACTTCTTC[C/T]GATATGTGTTTAGGG | 57630 |
| rs143778857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242787 | CTCTCTTGCTATATG[A/G]TGCCTTCTGCCATGT | 57630 |
| rs143782615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151092 | AAACATGTTTGTTTT[C/G]AGTTTAGAACCTTTC | 57630 |
| rs143810109 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200055 | AAATGGACTCCATCC[-/A]AAAAAAAGGAATAAA | 57630 |
| rs143830569 | in-del | -/GAGT | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209326 | CAAGTTATAGAAAAA[-/GAGT]GAGTGTCCTTTCAGC | 57630 |
| rs143833818 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113452 | CACTTTGCAGACCAT[C/G]TGGGAAATTCTAAAA | 57630 |
| rs143837840 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194467 | TATTTAAATGGATCA[C/T]GCAGGCTGTATTCTT | 57630 |
| rs143862731 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208928 | TAAGCAAGGGACTGA[A/C]AAAAAGAAAAAAAAG | 57630 |
| rs143874445 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234266 | GCATCTAGTGGGTAG[A/G]TACCAGGTATGCTGT | 57630 |
| rs143900749 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110172 | TTGAGCCCAGGAGTT[A/G]AGAGCAGCCTGGGCA | 57630 |
| rs143901764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237983 | GAGTCCTATTAGGTC[A/G]GGTTAGCAAGAATCC | 57630 |
| rs143922079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105129 | ACACTTTATAGTAAG[A/T]TTTCAAGTCGGCAAC | 57630 |
| rs143922086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156845 | TTACCAATAAATAGA[A/G]AACACAAAACAATTG | 57630 |
| rs143977928 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163017 | CTCAGCTCTTGACCA[A/G]ACAGCAATCAGTCAA | 57630 |
| rs144025259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240771 | ATTATTACTAACCAC[A/G]GTCACCATGCTGCAC | 57630 |
| rs144034469 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113068 | AATCTGGGATGAGGG[C/T]CAACTGAACAGGCAA | 57630 |
| rs144057292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159043 | TAATGACACCCTCCT[A/G]TGACCTCTGACTTTC | 57630 |
| rs144091276 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238430 | CTGCTGCCCTCTTAA[C/T]TTACCATTACCATGA | 57630 |
| rs144120791 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229475 | ACCACCCCCCCACCC[-/A]AAAAAAAAAACCTAT | 57630 |
| rs144122527 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118234 | ATGCACACACATACA[C/T]GCACTAGTGGAAAGT | 57630 |
| rs144187577 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157927 | TGTATTTTTACAAAA[C/T]GGGGTCTCGCCATGT | 57630 |
| rs144219958 | snp | C/G/T | 0.000478043 | 0.0154531 | missense | SH3RF1 | GRCh38.p7 | 4:169120979 | GAGTGTATGGATATA[C/G/T]AGCAACATACCTAGA | 57630 |
| rs144221789 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214758 | CTTCTAGTTTCATTT[A/G]TTGATGCCATATAGA | 57630 |
| rs144260194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218709 | ATTAGAGCAGCATTA[C/T]TGCCTTTTTATAGCT | 57630 |
| rs144286616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172252 | ATACAGAATGAGTAG[C/T]AGAAGAAGGCAGTTA | 57630 |
| rs144339794 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147600 | TCCTCTCAACATATG[A/G]AGGAATTTTCGCCCC | 57630 |
| rs144346060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214170 | TGAGTAGCTTGGTAC[G/T]GTCCTTGCAATAATG | 57630 |
| rs144367316 | in-del | -/TTCT | | | frameshift-variant | SH3RF1 | GRCh38.p7 | 4:169136427 | TCCATGGAGTGGCGG[-/TTCT]GGGATGCCTGGGAGG | 57630 |
| rs144400089 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264326 | CTTCTTATAAGAACA[C/T]TGGTCTTACTGGATT | 57630 |
| rs144425191 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135691 | GTCTGCCAAATGAAT[A/G]AATGAATGATTGAAT | 57630 |
| rs144441623 | snp | C/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271280 | TGCAAGAGCCTAGAG[C/G]ATGGGGAGCGGGGCC | 57630 |
| rs144449973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250619 | GTTCTACCTGCTGGG[A/G]ATACAGACAGGAATA | 57630 |
| rs144452780 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095923 | TACCCCAGGCCCTAA[C/T]TGATACTGATTCATT | 57630 |
| rs144481797 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226303 | CTTGGTTTGTCTTTC[A/G]CAGTCACTTGACATT | 57630 |
| rs144502162 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097862 | ACTTTCTCTTGGATC[A/G]GTCACTCAGGAAAAC | 57630 |
| rs144504544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148499 | TTACCAAAATTATAC[A/G]CGATGAGACTTAGGA | 57630 |
| rs144516359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122452 | ACAAATTCATCTCTT[A/G]TTCTCCTTTAAAATA | 57630 |
| rs144520457 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202771 | TTGAATCCCTTAGAT[A/C]TGTTGTTGTCATCAG | 57630 |
| rs144521097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230695 | GAAACTCCATCTCTA[C/T]TAAAAATACACAAAT | 57630 |
| rs144541976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144449 | CAGAATCAAACCTAA[C/T]GGAGCCTTTTACTCA | 57630 |
| rs144599726 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272923 | GAAAGCAAGGGACAG[G/T]TTTTATTGTGTTCTT | 57630 |
| rs144605961 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191186 | GATGCCCACCGTCAC[C/G]ACTCCTCTTCAACAT | 57630 |
| rs144629121 | snp | C/G | 0.00312695 | 0.0394169 | missense | SH3RF1 | GRCh38.p7 | 4:169156619 | TGCTGAATTTAAGGT[C/G]TCCAGGCTCTTTTCC | 57630 |
| rs144654339 | snp | A/G | 3.29625e-05 | 0.00405958 | missense | SH3RF1 | GRCh38.p7 | 4:169122122 | GGCGAGTCTGCGGCC[A/G]TAAATGTGCAATCTG | 57630 |
| rs144655670 | snp | C/T | 0.000461308 | 0.0151803 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117620 | GATGTGAGCTGCTGA[C/T]ACCACAGCTGCGGGG | 57630 |
| rs144667469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225635 | AAAGGTGACTGCAAT[G/T]TTAAAGGAAGTGAGT | 57630 |
| rs144675070 | in-del | -/AT | 0.15665 | 0.231917 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166167 | ACCACAGATTGGGAA[-/AT]ATATATATATATATA | 57630 |
| rs144681206 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111131 | ACATGGTGAAACCCT[A/G]TCTCTACTAAAAACA | 57630 |
| rs144707355 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233823 | ATTTCATTAAGAGAC[A/G]TAATTGAAAATCTAG | 57630 |
| rs144745847 | snp | A/G | 0.000198666 | 0.0099646 | missense | SH3RF1 | GRCh38.p7 | 4:169116445 | CTGCACAGGCCAGAG[A/G]GGCACTGGCTCGACT | 57630 |
| rs144776007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172128 | ACTCTGAAATTGATA[C/T]TGTATGAGCCTAAGA | 57630 |
| rs144791336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187679 | GACCAGGCAACTGCA[A/G]TCTATAAATTAGTTC | 57630 |
| rs144792617 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255237 | GCTACAAAATCAGTA[C/T]GTGAATATTTTAACT | 57630 |
| rs144800001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253197 | CCTAGAAACCACAGC[A/G]TGGCACATTTCTAAA | 57630 |
| rs144817324 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248597 | CACCATGGCACATGT[A/G]TATCTATGTAACAAA | 57630 |
| rs144841019 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255729 | GCATTAAAACATCCA[C/T]GTTTTAACAATGGGC | 57630 |
| rs144854345 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251653 | AATGGAATGCACTGG[G/T]AGCGGTCCCCATCTC | 57630 |
| rs144878980 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130735 | CAATGTCAAGCCAAA[C/T]TAGTTGTTTTCAAAG | 57630 |
| rs144910796 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128783 | TAAAATCTTTACAAC[A/G]TGTATAAAACCCACA | 57630 |
| rs144915817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126382 | CTGATTTTTAGATCT[C/T]CTGCCAATTCCAAAG | 57630 |
| rs144920327 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129567 | GAAGGTGCCTTTAAA[-/C]CAGCCACAGCTACAG | 57630 |
| rs144923998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206426 | ACCCATAATTCCAGT[A/G]CTTTGGGAAGCCAAG | 57630 |
| rs144931015 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209858 | GCAATGACACAATCA[C/T]GGCTCACTGCAGCCT | 57630 |
| rs144931634 | in-del | -/AAGT | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156765 | GTTGTCATTGTTTTA[-/AAGT]CAAAGTCAAAACCAC | 57630 |
| rs144948802 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123750 | CAAAAAAATTAGCCG[A/G]GTGTGATGGCGGGTG | 57630 |
| rs144949994 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125029 | CCTTCTAGAAAATGA[C/G]ACAAAATTCACATTT | 57630 |
| rs144957153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203989 | TACTATGAAGAAAGC[A/G]CCTGGCATAATCTTG | 57630 |
| rs144983953 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260528 | TGCTAAAGCCAGAGA[G/T]CCAGGGCAGAGGTGG | 57630 |
| rs144988142 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102524 | TCTTTATATATATAT[A/T]TTTTTTCTTTGGAAG | 57630 |
| rs144988399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231895 | GTCTTTAAAAACCTG[C/T]TATTCTAGAAGGAGA | 57630 |
| rs145003717 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215854 | CATCGCACAGGCTGG[A/G]GTGCAGTGGTGCAAT | 57630 |
| rs145006915 | snp | C/T | 0.305934 | 0.243663 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145998 | CTATATAAAATATTA[C/T]ATATTCTATATATTC | 57630 |
| rs145008810 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149209 | GAAGCCTCTGAATAA[C/T]AGATGGAGCATAAAC | 57630 |
| rs145068153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130415 | CAGAATTCAACTGCC[A/C]TTGGCTTTCACGGTA | 57630 |
| rs145175806 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138967 | TATTTTTGGGGGGAC[C/T]GGGGGGAAAGGTCTC | 57630 |
| rs145196664 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252132 | CACTTAAGAGGGCCT[A/G]CGTTTTCACATTTTA | 57630 |
| rs145201422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103519 | TGATATAAAAGTTAA[A/T]CTTTCCTTCATTTTC | 57630 |
| rs145203029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184147 | CAGGGCACTCCCACC[A/G]GCAGGCTTACTGTGA | 57630 |
| rs145232877 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227017 | ATAAAAAGTGAAAAA[C/T]TAGCCAGGCGTCGGG | 57630 |
| rs145287011 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106206 | CAACCTCTGCCTCCT[A/G]GGTTCAAGCGATTCT | 57630 |
| rs145291489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124753 | TGTGACAGACTAGGA[A/C]ATTTTGTGGGTTGCT | 57630 |
| rs145292880 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188913 | TTATCAATGTACCAC[C/T]TGTAACTGACTTTTT | 57630 |
| rs145307093 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102522 | ACTCTTTATATATAT[A/T]TTTTTTTTCTTTGGA | 57630 |
| rs145312383 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184804 | GTACAATCTAAATCA[C/T]ATCTTGATTAGCATC | 57630 |
| rs145324505 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101927 | TCCACAGACTTCCAA[C/T]GCTATGGTATTTTAA | 57630 |
| rs145336773 | in-del | -/TC | 0.10237 | 0.201756 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123239 | ACCAGTCATCTTATT[-/TC]TGTTTTTTGGAATAA | 57630 |
| rs145371295 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107673 | TCTAATTACTGTAAG[A/T]GAGCTGACTATGCAG | 57630 |
| rs145382708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199782 | ATGGATAAAAAGGTG[C/T]GACAAATATAAATAA | 57630 |
| rs145405150 | snp | A/T | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169268936 | TTAATGCATTTGTGC[A/T]GTTGGTCCCACTTCC | 57630 |
| rs145468705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113323 | ACTATGTTGGCCAGG[C/G]TGGTCTCAACTCCTG | 57630 |
| rs145512800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249758 | AGGAAGCAAGTGCAG[A/T]TTAAAGTACAGTAAC | 57630 |
| rs145535876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235656 | CATTACATCAGCAAT[A/G]AGCATATATTATAAA | 57630 |
| rs145544864 | snp | A/G | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169130120 | CTGGGCTGCTTGGGG[A/G]CGGGGTCACAATTAA | 57630 |
| rs145561500 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169477 | TGGTGCATACCTGTA[G/T]TCCCAGCTACTTGGG | 57630 |
| rs145566255 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256424 | CCAGTGTCACACTAT[A/C]GTCGTAAAACCAGAA | 57630 |
| rs145571212 | snp | A/G | 0.00218228 | 0.0329602 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106933 | AGCGATGGGAACTGC[A/G]GAGTCCAGGGAACTT | 57630 |
| rs145575230 | snp | C/G | 0.046775 | 0.145601 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190727 | AATCATTCTATGAAG[C/G]CAGCATCACCCTAAT | 57630 |
| rs145601248 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164979 | AAGTAAAATGCAAGA[A/G]GTTTGTGTCACTCAT | 57630 |
| rs145651043 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167562 | CATCAACATGGGAAT[A/C]AATGGAATCCTGTTT | 57630 |
| rs145695215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097333 | CAGACATGGAGGGGA[A/G]GGCTATGGCCACAAG | 57630 |
| rs145700315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179682 | TCCTGAGAGCCCCAC[C/G]CAAAGACAACACTGC | 57630 |
| rs145713939 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211593 | GCACTTGTCTACTAT[A/G]AATAAGGGACGAGTC | 57630 |
| rs145729765 | in-del | -/AACTCCAC | 0.369046 | 0.234143 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241570 | ACATCAGCACTCCTG[-/AACTCCAC]AACTCCACCAGAGGA | 57630 |
| rs145737185 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163906 | ATGACTGCTTTTGTT[G/T]TTTGGAATCAGGTGT | 57630 |
| rs145779154 | in-del | -/T | 0.0807149 | 0.183963 | | | GRCh38.p7 | 4:169250812 | AGTGAGGGGTGGGGC[-/T]TTTTTTGGATATGGT | 57630 |
| rs145786012 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 4:169257051 | AATCCTCACAAACTT[A/G]GAAAGCAGCTCTTCA | 57630 |
| rs145824726 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261298 | CACTGTCATTGTAAA[A/G]GAGCTTTATTTGTCC | 57630 |
| rs145849076 | in-del | -/G | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139812 | CCATTACCTAACTTT[-/G]GGGCCTTAAGGGAGC | 57630 |
| rs145854781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228469 | CTGCATCACTTGCCT[C/T]GGGGCCCCTTCCTCC | 57630 |
| rs145871058 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134730 | TCACACGGATATGAT[A/T]AGTTAAATGTAAAAT | 57630 |
| rs145883162 | snp | A/T | 1.64817e-05 | 0.00287064 | missense | SH3RF1 | GRCh38.p7 | 4:169156498 | GGCTGAGGTAACGGT[A/T]TAATAATCTGCACAA | 57630 |
| rs145894569 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149788 | GATGCTATCTTTTTA[A/T]ATAGTTCAATCAACT | 57630 |
| rs145914260 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140136 | CCTGTATCAGTTCCA[G/T]AGAAAATCATAAAGT | 57630 |
| rs145914591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147147 | CTGGTTCTGACAATA[C/T]ATGAAGTTTTATATA | 57630 |
| rs145983714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247107 | AGAGTAAGACATGAT[A/G]TGCTCACTGGGAAAA | 57630 |
| rs145990699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121368 | CTTGAGAAGTAGCCC[C/T]AAATGAGAACATATG | 57630 |
| rs145992964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202325 | TAGTTCTTGGTATGA[C/G]GTCAACCTTGACTCT | 57630 |
| rs145995216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250073 | ACCCACTCCTTAAAC[A/G]GTTTTAGGTACAAAA | 57630 |
| rs146002278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118245 | TACACGCACTAGTGG[A/G]AAGTCCTCTCCGTCT | 57630 |
| rs146004104 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198309 | TAACATCCCCAGTTA[C/T]ATTAATATTAGTGTT | 57630 |
| rs146014701 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221080 | ATCAGAAATGAGAGG[A/C]GCACATAGCATTTTA | 57630 |
| rs146038826 | in-del | -/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271449 | CCGCCGCCTCCTCCT[-/C]CCCCCCGGCGGGGCT | 57630 |
| rs146111917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101420 | GAAGTCACTTACGGG[C/G]AGAGAAAGTAGAAGG | 57630 |
| rs146118380 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228784 | TTTTATTTTTCATAC[A/G]GACTCACAGACATAT | 57630 |
| rs146124616 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096122 | GCTTCTCCTTACCTA[A/T]CATTTCATAAATTAA | 57630 |
| rs146127151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178822 | TCCAGATCAACACAA[A/T]CTGCTCTCCCCCAAA | 57630 |
| rs146178713 | in-del | -/TACACTCTCTAC | 0.10237 | 0.201756 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124979 | ACCAGAGGCCAAGTA[-/TACACTCTCTAC]TACAGGCAAAAAACA | 57630 |
| rs146246110 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158676 | TAGTTGAATATTTTT[G/T]AAGTTTAATATTTCC | 57630 |
| rs146248693 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244639 | CCTGACTAACCAAAA[C/T]GTAGGTAGAAAGAGT | 57630 |
| rs146254408 | snp | A/G | 1.67534e-05 | 0.0028942 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117758 | AGACATAGGGACTTT[A/G]GCTTGGGAAGCATTT | 57630 |
| rs146265575 | snp | C/G | 8.4163e-05 | 0.00648648 | missense | SH3RF1 | GRCh38.p7 | 4:169107007 | CTGCAGTCGTGACCG[C/G]TCCGTCCCCGTCCAC | 57630 |
| rs146269274 | in-del | -/CG | 0.129664 | 0.219133 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181549 | ACAGGCGTGAGCCAC[-/CG]CGCGCCAGCCCTGGG | 57630 |
| rs146346246 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263078 | TCCAAACCACCACAT[A/T]AAATGTCTTGCTTGG | 57630 |
| rs146348154 | in-del | -/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228387 | GTTGGCAGCGCTGTG[-/G/T]GTTTTTTTTCTGGAG | 57630 |
| rs146358935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265920 | GAACTACTTAAAAAC[C/T]ATGCTTTCCTTATCT | 57630 |
| rs146367077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138224 | GAAGCAAAGTAATGC[A/T]TTATATTATAGTGGG | 57630 |
| rs146370452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222808 | ACTTTAATGGAACAT[A/G]TTTATTCCTTCCTGC | 57630 |
| rs146375577 | in-del | -/TA/TATATA | 0.561178 | 0.110656 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173999 | TGTAATTTCCTGAGT[-/TA/TATATA]TATATATATATATAT | 57630 |
| rs146400483 | in-del | -/A | 0.163922 | 0.234714 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156684 | TGAGGTATACCCTTT[-/A]AAAAAAAAAGAGGGA | 57630 |
| rs146403033 | snp | A/T | 0.00795532 | 0.062565 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095208 | TGGTTAACTCATCCT[A/T]GATGTCTGTCTGCTG | 57630 |
| rs146405911 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238004 | GCAAGAATCCCCCTA[C/T]ACTTGATGTCTCCTC | 57630 |
| rs146411221 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145026 | AGAAATGAAAAAGGC[-/A]AAGAGTTTCAGAGAG | 57630 |
| rs146416267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108228 | CTTCATAGAGAACTA[C/T]TTCTTTAGAAAATTC | 57630 |
| rs146419401 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191180 | GACAAGGATGCCCAC[C/T]GTCACCACTCCTCTT | 57630 |
| rs146439620 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194233 | AAAGCATATAAAACT[A/G]CACAAAACCAAGATG | 57630 |
| rs146466853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113119 | CAGTTTTCTTTTTTT[C/T]TTCCCCCCTGAGACA | 57630 |
| rs146468875 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242867 | CTTCCCAGCCTCCAG[A/T]ACCATGAGCCAAATA | 57630 |
| rs146506519 | in-del | -/A | 0.0383715 | 0.133092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249243 | AAAAAAAGAAAAAAG[-/A]AAAAAAAAGAGGCAA | 57630 |
| rs146539862 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214906 | TTATCATGTCCTCTG[C/T]AAACAGACATTTTTA | 57630 |
| rs146541625 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115425 | CAGGGGCATTAGATT[C/T]TCATAGGAGCATGAA | 57630 |
| rs146543023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168964 | ACAGAAATCAAATCA[A/T]GCCAGCTTCAATACT | 57630 |
| rs146550580 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219524 | CGCTTACAAAAAAAA[A/C]CAAAAACCCCCAAAA | 57630 |
| rs146592218 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172407 | TTTACTTCCTTTCTT[A/C]TTCCTTTATCATGTA | 57630 |
| rs146661296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199327 | AGTGGCTTAACACAT[C/T]ATTCTCATAACAGTC | 57630 |
| rs146661363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149291 | TATTTATTAAACAGC[C/T]GTTCCTGGAGCTCAG | 57630 |
| rs146672138 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194302 | GAACAACCACCAGGA[A/C]AAGACACAGAGTTTG | 57630 |
| rs146678525 | in-del | -/G | 0.168135 | 0.236216 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165637 | CAGAGAAAAAAAGGC[-/G]GGGGGGGGGAGTCAG | 57630 |
| rs146684405 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119941 | TTCTTTCCTCAGTGA[C/T]CAAAAGCTGAACTAT | 57630 |
| rs146704235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199895 | GATATTATAATGTAT[A/T]TTAAAACAATAACAA | 57630 |
| rs146710065 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152353 | TATAGCCATTCTTTC[C/G]CCTACTCACTTCTCC | 57630 |
| rs146777014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196170 | ATGAAGCTTTAATGT[A/G]TTTTTTTCTATTGCT | 57630 |
| rs146789875 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259958 | TTTGACCTTAAAATT[G/T]TAAAGTCTTTTTACA | 57630 |
| rs146830698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214281 | GAGGTACCTGCTCCC[A/G]CTTCATTGTCTGCCA | 57630 |
| rs146946574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221859 | CAAAATCGTTACACA[A/G]TACAAACAGTGAACT | 57630 |
| rs146956107 | snp | C/T | 0.00517822 | 0.0506191 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093915 | TTACGGGTTATCATA[C/T]TATTGGTTGATAGGT | 57630 |
| rs146984385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174188 | TCTCTTCAGCCCCTC[A/G]AAAGCTGTGACTACA | 57630 |
| rs147029784 | snp | C/T | 0.106987 | 0.205054 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197454 | AACATTGTGAAACCC[C/T]GTCTCTACTAAAAAC | 57630 |
| rs147072229 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200972 | TCTTCAGTGTGCTCT[C/T]GAGCCAGTCAGACAC | 57630 |
| rs147078784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159965 | TTCACTGACATGTAC[C/T]GTTTAATAGGGGATG | 57630 |
| rs147085211 | in-del | -/CATCCC | 0.0232847 | 0.105357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263113 | GTATGAGTTAATACA[-/CATCCC]CATCCCCATCCCCAT | 57630 |
| rs147088277 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156236 | TCTGTGCATAAAATT[A/G]CCTTCCTTGTGACTT | 57630 |
| rs147088585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205042 | CATTAAAAGGGAAAT[C/T]TACTAGCAACATGCA | 57630 |
| rs147117658 | in-del | -/CAG | 0.0225045 | 0.103662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103703 | ATTTTTACTGTGAGA[-/CAG]CAGATCTAAGAATCC | 57630 |
| rs147133099 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128682 | AACAATAAAACTAGC[C/T]GGAGCCAACATTTTG | 57630 |
| rs147133180 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177175 | AATTCAATTATTACA[A/C]AGCAAATAAGGGATG | 57630 |
| rs147135476 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255030 | AGTACATTGCAAGGA[C/T]AGGAATTTATGTTTA | 57630 |
| rs147142758 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171572 | ACAGCAGAAAAAAGG[C/T]TTTACATTTCTAAGG | 57630 |
| rs147175661 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132276 | TTATTGATTGACATT[C/T]CTCTAAAAGCCCAGA | 57630 |
| rs147231849 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189113 | TCTTGTCAGTTCAAG[C/T]AGAAGCTTTTGTAAA | 57630 |
| rs147237924 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105195 | AAGCAGAAATTTGCT[C/T]TATTTATGAAATGCA | 57630 |
| rs147247247 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151160 | ATATTTATTGAAAGC[C/G]TACTACAGGCGCTGT | 57630 |
| rs147280929 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110182 | GAGTTGAGAGCAGCC[C/T]GGGCAACATAGCAAG | 57630 |
| rs147283623 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192242 | CTCAGGACATGAATA[C/G]ACAGTTCGCAAAAGA | 57630 |
| rs147337585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251415 | AGCAGCCTTAAAATC[A/G]TGCACAAAACAAGAT | 57630 |
| rs147338242 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167671 | AACAGGTGAAACGAA[C/T]CTCTTGTGGTAAAAA | 57630 |
| rs147346380 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167057 | TCCTCAGCTCCAGGG[C/T]TACCTATAATCTGTG | 57630 |
| rs147348675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213134 | CCAAAGTGACTGTAC[C/T]ATTCTGCATTTCCAC | 57630 |
| rs147389124 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171218 | TGTTTCTGTACCTCA[C/T]TTCTGTTTTCTGTGA | 57630 |
| rs147402241 | in-del | -/TT | 0.0185938 | 0.0946107 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151465 | GTAGTAGAGTCAAGA[-/TT]GGAATCCTGGCCATC | 57630 |
| rs147443414 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230811 | CAGTGAGCTGAGATC[A/G]TGCCATTGCACTCCA | 57630 |
| rs147460447 | snp | G/T | 0.135825 | 0.222405 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192880 | TATATATATCATATA[G/T]ATGTGATATGTTTCT | 57630 |
| rs147466303 | in-del | -/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148171 | AAAGTTGGATAATAA[-/T]AGTGATTCTGCCCAA | 57630 |
| rs147478073 | snp | A/G | 0.000115396 | 0.00759505 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122138 | TAAATGTGCAATCTG[A/G]TCAGTGGATCCTGCC | 57630 |
| rs147493521 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150891 | AAAATTCTAAACTAG[A/G]TACAATCAAATAGCC | 57630 |
| rs147548901 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210336 | ACCTTCTAATTCACA[A/T]GAAGACAAAACACCT | 57630 |
| rs147564372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123073 | CTGAACCGCTACCTC[A/G]TCCTCTCCAGATCTT | 57630 |
| rs147611066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184837 | CTAAACCTAAACTGG[A/C]CTAAGCAGTAGAAAA | 57630 |
| rs147616582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263838 | TCATTTCCTCCAGAA[C/T]TTTCTGTGCATCTGG | 57630 |
| rs147650398 | in-del | -/TA | 0.136506 | 0.222754 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192797 | CATATATGTTTCTTT[-/TA]TATATATATGATATA | 57630 |
| rs147653742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139354 | TAAAAATAACACAGT[A/G]CTTTCCATAATTTCT | 57630 |
| rs147669754 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102295 | TCAAAGAAATTAATC[A/G]TGCTGGTTAAGCCCA | 57630 |
| rs147711918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242855 | CTCAATCTTGGACTT[C/T]CCAGCCTCCAGAACC | 57630 |
| rs147715417 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163431 | AGCATGTTTAAAAGG[A/C]AATGTTGCAGGAAAA | 57630 |
| rs147744713 | snp | A/G | 3.34146e-05 | 0.00408732 | missense | SH3RF1 | GRCh38.p7 | 4:169116516 | AGAGGCGCAGGTTGT[A/G]GGGAGGCCAGCGAGT | 57630 |
| rs147756978 | snp | C/T | 0.10237 | 0.201756 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119142 | GGAGTCTTGCTCTGC[C/T]GCCCAGGCTGGAGTG | 57630 |
| rs147774891 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163084 | CATTAATGGTTTCGG[G/T]GGCAAGGTAGAGGGA | 57630 |
| rs147806982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264442 | GAGTTAGAACTTCAA[C/T]GTAGCAATGTTGGGG | 57630 |
| rs147817013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221086 | AATGAGAGGCGCACA[C/T]AGCATTTTATACTGT | 57630 |
| rs147817159 | snp | G/T | 0.0205511 | 0.0992634 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271611 | CCGGACACTTACTTG[G/T]TAGAGTCGGAGCGAA | 57630 |
| rs147826753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226389 | TCGTGTCTACATATC[A/C]AGGTTTTCCTGGTCA | 57630 |
| rs147862302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097995 | ATGTGAATAAGCCAT[C/T]TTAGAAGGGGATCCT | 57630 |
| rs147876415 | in-del | -/GACCATCTGGAA | 0.0217236 | 0.101931 | cds-indel | SH3RF1 | GRCh38.p7 | 4:169096422 | CTTTGCTCATCTCCT[-/GACCATCTGGAA]GTCCACAAATGTGCT | 57630 |
| rs147879923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143988 | AGGAAAAGCCCTGAA[C/T]TTCACACCGAAAGGT | 57630 |
| rs147893762 | in-del | -/TTAT | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122812 | TGTTGCTACTTTTGC[-/TTAT]TTATTCTTTTCTTAA | 57630 |
| rs147913581 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248678 | ATTCAAAAAAAGTAA[C/T]AGGAAAAGGGGAAAC | 57630 |
| rs147918956 | in-del | -/AAC | 0.161267 | 0.233723 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120713 | AAACCTTGGCTATGT[-/AAC]AACAGGCAATTATAA | 57630 |
| rs147921585 | snp | C/T | 1.65748e-05 | 0.00287874 | missense | SH3RF1 | GRCh38.p7 | 4:169116451 | AGGCCAGAGGGGCAC[C/T]GGCTCGACTGATACT | 57630 |
| rs147923439 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251728 | ACCTATAAGGAATGC[A/T]TCAGTGACATGGAAC | 57630 |
| rs147924465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123944 | TGTACTGAGGCTTAG[A/G]GCCTCCAAAACCTTT | 57630 |
| rs147936754 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200308 | TCCAAAACCTGTTTA[C/T]ATGTTAAGCCACAAA | 57630 |
| rs147968175 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166788 | CCGGCTCGTTACTTT[-/G]GACTGGACCTCTGGT | 57630 |
| rs147986774 | snp | A/C/G | 0.000299185 | 0.0122273 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116569 | AGGGCTGAGGCCGGC[A/C/G]GCATTCTGTACCTGG | 57630 |
| rs147988327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136207 | CCAGAAAAGTTACTA[C/T]CTTCAGAAGTTCAAA | 57630 |
| rs148016263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256756 | TGCATGCCACCATGC[C/T]CAGCTAATTTAAAAA | 57630 |
| rs148025970 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212599 | CAGGAAGTACAGAGA[A/G]TTCCCATATACTCCT | 57630 |
| rs148038196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098974 | GAGGTGAAGAATGGG[C/T]CAGTCAGTGGCTGGA | 57630 |
| rs148040332 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131171 | CACTGGGGTAGGCCC[A/G]ACCAAAGCCAGGCAT | 57630 |
| rs148078314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249268 | AGGCAATTAGGCCAT[A/G]AGGGCTCCTCCCATG | 57630 |
| rs148083566 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120572 | AACCTTCTCCCATTA[A/T]AGCAAATAACTTAAA | 57630 |
| rs148085534 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201272 | AGCTGGCTTTAACAA[C/T]TGACGAATACTTATT | 57630 |
| rs148104552 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187831 | CATATCTAGCTGGTA[C/T]CTCAGAATGCAGCCT | 57630 |
| rs148112842 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234174 | CCACCTGCCAGGAAC[A/G/T]TGTGACAATGTCAAT | 57630 |
| rs148138074 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195100 | ATTTCCTTTAGCTAA[A/C]GTCTGTTTGTTGGTA | 57630 |
| rs148154534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150032 | AGCTAGCACCCCCAC[C/T]TTTAAGGCCACTTGT | 57630 |
| rs148157050 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182357 | CAGTTGCTTGTGCAT[G/T]ATAACAGAGTGTAAT | 57630 |
| rs148198660 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095117 | GGCTCTTCTGGATCC[C/T]GCCACAATTGTAAGG | 57630 |
| rs148201453 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177516 | AGCACACAATAAATT[C/T]GTAAATGCAATAAAA | 57630 |
| rs148253832 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170700 | TCTTCCTTCATTCCA[C/T]CCTATATAGATCTGC | 57630 |
| rs148296319 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160611 | ACAAACATTTGTGCA[C/T]CTGGCTGTGTTTTTC | 57630 |
| rs148306233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206023 | AACTGATAGTTTTAA[A/G]TGGAATACATAGTGA | 57630 |
| rs148357500 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208208 | CCCTCCTTCATCCCC[A/C]CCCCCACTGCCTGAC | 57630 |
| rs148364234 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109814 | CAGGAGTTCAAGACC[A/C]GCCTGGGCAACATAG | 57630 |
| rs148385326 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222428 | TGAGATTGCACCACT[A/G]CACTCCAGCCTGGGT | 57630 |
| rs148391947 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250656 | ATCAAAGTCCTGGTT[C/T]TCATGGAGCCTACTG | 57630 |
| rs148401811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122754 | CCTTTGATGCCTGGT[C/T]TACAAAAAGCCCAAA | 57630 |
| rs148472676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151188 | TGTGCAAAGACCCTG[C/T]GGAACCGGCCCTTGG | 57630 |
| rs148482217 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197837 | TAGAATAATATTATA[C/T]TATATCCCTTTAAAA | 57630 |
| rs148486491 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263528 | GCTGGCAGTTGCTTT[C/T]CACACCAAACCTGGA | 57630 |
| rs148493340 | snp | C/T | 0.000926401 | 0.0215022 | missense | SH3RF1 | GRCh38.p7 | 4:169107034 | CCACAGGGCAGGAGC[C/T]TGCCCTGCCATGGCC | 57630 |
| rs148518280 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180433 | CTTAACACACTGCCA[C/T]AACCGGAGGAATTTT | 57630 |
| rs148523239 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104752 | ACTGAAAATACAAAA[A/C]AATTAGCCGGGCGTG | 57630 |
| rs148548488 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255332 | CACTGTTGCAGCATT[G/T]GCAAAATGCATCAGT | 57630 |
| rs148559828 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129026 | CCTTTTCCATGGTCA[C/T]ATAACAAATAAATGG | 57630 |
| rs148569398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172142 | ACTGTATGAGCCTAA[C/G]AAAGCAAGAGCTGAA | 57630 |
| rs148628694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118383 | TTTCATGTGGATTTC[C/T]TCTTTCATTCTGTTT | 57630 |
| rs148638366 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163036 | GCAATCAGTCAATTA[C/T]AGTCTCCAGCAGCCT | 57630 |
| rs148680465 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111180 | GGTGGTGCATGCCTG[C/T]AGTCCCACTACTTGG | 57630 |
| rs148689147 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238508 | TTGTCCTGATAGATG[C/T]CTGTGAGGTAGGCAG | 57630 |
| rs148696764 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225675 | GAAATGTGGATGAGC[C/T]TACACTATTTTTCAA | 57630 |
| rs148705588 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220317 | TGACACTTCACATGA[A/T]GATTGAAGAAGAATA | 57630 |
| rs148721890 | snp | A/C/T | 0.00159757 | 0.028218 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122117 | ACTGGGGCGAGTCTG[A/C/T]GGCCGTAAATGTGCA | 57630 |
| rs148733610 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148010 | GTTTTAATTAGTTTG[C/T]GATTTTTCTCATAAA | 57630 |
| rs148759534 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214199 | TGAGTGAGCTCTCAC[A/G]AGATCTGGCTGTTTA | 57630 |
| rs148776536 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101451 | GTGGTTGCAGGGCCT[A/G]GAGGAGGGGGAATGA | 57630 |
| rs148798269 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167825 | CAAAACCTACTAGAT[C/T]GTACACTTAAGAACT | 57630 |
| rs148836903 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146247 | CTTTTTTTTTTTTTT[-/T]GAGACCAAGTCTCGC | 57630 |
| rs148844095 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190761 | AAAACCAGGAAAGGA[C/T]ATAACCAAAAAAGAA | 57630 |
| rs148887040 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144996 | TTCCCAGGCCAACCA[C/T]CCAACCAACGACCCA | 57630 |
| rs148888477 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256481 | AACAGCTTGGGTATC[C/T]GAAGTTTAAGCCAGC | 57630 |
| rs148905228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130839 | TGTGTTAAGTTACTC[A/G]ATCAATTTCACTCAG | 57630 |
| rs148936586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097772 | GGATGACCTGTGTGG[C/T]CAATAAAATGTTGCA | 57630 |
| rs148947910 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120467 | CATATAGTACGCATT[A/G]TATAAACACATAAGT | 57630 |
| rs148950054 | snp | C/G | 0.125182 | 0.216612 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249010 | AGGTGGGCAGATCAC[C/G]AGGTCAGGAGATCGA | 57630 |
| rs148957898 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164163 | AGTTTATAACCTATT[C/T]CTTCCTGCTAGACTG | 57630 |
| rs148999671 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113399 | ACAGGTGTAAGCCAC[A/C]GCGCCCGGCCCCAAT | 57630 |
| rs149001583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194392 | ATGCAACCACAATCA[C/T]GGCTTTTGCCTAAGT | 57630 |
| rs149010427 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228349 | TCAGAGTACAAAATG[G/T]GTCTCTCTGAGCTAA | 57630 |
| rs149064631 | snp | C/G | 0.0333695 | 0.124785 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231951 | TTAAAATTTTTTCCT[C/G]TAATGGAGACATATT | 57630 |
| rs149094170 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102688 | TTCTGCTGTCATCAA[G/T]TATACATTTTCTGCC | 57630 |
| rs149098537 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216216 | CATATTCTTAGTTTG[G/T]TATAACACATTTGGA | 57630 |
| rs149115215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169891 | GAGGCTTTAAAAATA[C/T]TTTGTAAATATTCTG | 57630 |
| rs149147737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139090 | CTGAGTAGTTGGGAC[C/T]ATAGGTATGCAACAC | 57630 |
| rs149151138 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252133 | ACTTAAGAGGGCCTG[A/C]GTTTTCACATTTTAT | 57630 |
| rs149166146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124916 | TTCATTCACCCGGAG[A/G]TGACCTGGAGTCCTG | 57630 |
| rs149168746 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205859 | TTGAGAAAACAAACA[G/T]GTATCCAAAGGAGAT | 57630 |
| rs149211653 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152662 | GAATTGCTTGAACCC[G/T]GAAGGCAGAGGTTGT | 57630 |
| rs149220551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265401 | GCATCATGAAATCAT[C/T]AAGTAATAATATCTA | 57630 |
| rs149220793 | snp | A/C/G/T | 8.39142e-05 | 0.00647702 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116527 | TTGTGGGGAGGCCAG[A/C/G/T]GAGTGATGGGACAGG | 57630 |
| rs149221558 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199825 | AGGTGACAGTAACAA[C/T]ATCAAACATTCAGCA | 57630 |
| rs149258054 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181694 | TCTACTTTATGTGGA[G/T]AATTAATACATTCAT | 57630 |
| rs149263883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250577 | GTTAACAAATTCTTA[C/T]TGAGAACCTACTATG | 57630 |
| rs149266412 | snp | A/G/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121952 | CCCTAGTTACATGCA[A/G/T]GACCAGGTAGAAGTT | 57630 |
| rs149276512 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165860 | TTCAACTGAGAAAAA[C/T]AAAGTCTTTTCAAAA | 57630 |
| rs149316992 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243950 | TGCAAACATGGCAAG[C/T]TACCCTGGAGTTGCC | 57630 |
| rs149320891 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197602 | GTACTCCAGCCTGGG[C/T]GACAAAAGCAAGACT | 57630 |
| rs149362557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110324 | ACCACTGCACTCCAG[C/T]CTGGGTGACAGAGTG | 57630 |
| rs149379992 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233762 | CCTATTATTTCACAG[A/G]ACCATTACTCTTTCA | 57630 |
| rs149414555 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217589 | AAGGTGTACAAGACA[A/G]GTTACTAAACCAGGG | 57630 |
| rs149415257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104207 | GGGCAAAGTGAACCA[C/T]CACTCAAAAGAGTCA | 57630 |
| rs149469254 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141463 | TTGCTAGATCAAAGT[G/T]TAAGTTTAAAAATCG | 57630 |
| rs149469877 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222325 | AAAAAATTAGCCAGG[C/T]ATGGTAGCAGACACC | 57630 |
| rs149480392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162975 | AGCTCCTGCAATCCA[A/T]TCCACCATCGCTAAT | 57630 |
| rs149484684 | snp | A/G | 0.000153988 | 0.00877327 | missense | SH3RF1 | GRCh38.p7 | 4:169106910 | GAACAGGCCTGGCGA[A/G]GAGGTGGAGCGATGG | 57630 |
| rs149486210 | snp | C/T | 0.0138799 | 0.0821421 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095015 | CCTCCTTTTGTTTTC[C/T]GGACTACCCAGATCC | 57630 |
| rs149490335 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208600 | ATCTTAGTTATACCA[A/G]TTTCACTCTGTCTTA | 57630 |
| rs149532154 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157842 | TGCCTCCTGGGTTGA[C/G]TGATTTTAACGCTTC | 57630 |
| rs149538079 | snp | C/T | 6.59935e-05 | 0.0057439 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169120854 | ATTGCCAGGGAAAAC[C/T]CCTATCTTGCTGGTA | 57630 |
| rs149538473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238335 | GAAGGATGTGAGGAA[C/T]GCTAGCACTGGCCAA | 57630 |
| rs149623945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258450 | ATTTCAGACTTGTTT[C/T]ACAAAAATGAGTAGA | 57630 |
| rs149692854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235579 | GCCTAACTCAATAAC[G/T]CAATCCACATTCTTC | 57630 |
| rs149707336 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106585 | TTGACAGTTTTTACC[A/C/T]GGACACAATTCAGGC | 57630 |
| rs149709281 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189946 | AAACCATGCAAATAC[A/T]TGGAAATTAAATAAC | 57630 |
| rs149771927 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270832 | ACGCTGGGTCCCCGT[C/G]GACCCCGCGCCGGCC | 57630 |
| rs149850339 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159263 | CTCTACCCTCACAGA[C/T]GCCTCATTATATTCT | 57630 |
| rs149855649 | snp | A/C/T | 0.000317789 | 0.0126021 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136543 | GCTCTGGGCTGCTGC[A/C/T]GAGGAACATTCTCCA | 57630 |
| rs149857912 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171901 | GGGTCTGGTGAAAGG[C/T]TATATCTGCTTCTTC | 57630 |
| rs149903538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193689 | ATGTATAATAAGGAG[A/G]TAAGGTCTCACCACA | 57630 |
| rs149920225 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148612 | TGGCTCTAAGAAACA[C/T]AGGAAAATAATAAAT | 57630 |
| rs149991659 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263330 | CCTGATGCTTCACTA[A/T]CTGCTGCCTTACTTG | 57630 |
| rs149999509 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251942 | CAAAACTATATTTTA[C/G/T]TCAGATCACCTTTGA | 57630 |
| rs150015092 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138560 | CTCCTGTCCCAGTGA[A/G]TAAGAAGTAGAGGAG | 57630 |
| rs150017608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168945 | TGAGAATATGAATTC[A/G]CCTACAGAAATCAAA | 57630 |
| rs150061269 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199507 | CTCCCTAAAAGCCTT[A/G]GCCCCAACATGGTAA | 57630 |
| rs150066928 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133115 | TAGAAACCAGGGCAT[A/G]AGGACCCACTTATAT | 57630 |
| rs150094812 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228050 | TACTATTTTTGTTCA[C/T]GTAGTTACCTCCCTA | 57630 |
| rs150120873 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099907 | ACAGTCTTGATCGTA[C/T]GAAGACTACCAGGTG | 57630 |
| rs150175813 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173963 | CTGACTTTAAGGATA[C/T]GGCTAATGCTAGTTC | 57630 |
| rs150195247 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201644 | AGGCAGCTTATTTCC[A/C]AGTCAAAGTTATAAT | 57630 |
| rs150218614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163658 | CATTAATGGTCTAAA[C/T]CATGAGTTTTATGGC | 57630 |
| rs150237185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150457 | GAGCTAATTAACATA[C/T]GTATTACCTCAGATA | 57630 |
| rs150251422 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233276 | AAAAAAAAAAAAACC[A/G]TGGTTTACTCAGAAC | 57630 |
| rs150289101 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186291 | GTATAACAAACCCCA[C/T]GACACATGTTTACCT | 57630 |
| rs150303190 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264962 | CCCTAATTAATATCA[A/T]TTCACCCTTAAGATC | 57630 |
| rs150310553 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254531 | ATTGCTGACACTATC[A/G]TAAAGATTACAGAAA | 57630 |
| rs150332042 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141067 | CAATTCTTCTTCCAA[A/T]GTGATCCAGGGAAGC | 57630 |
| rs150356731 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260301 | AGCATTTTGAGAAGA[C/T]AACCCAGAGAAGCAG | 57630 |
| rs150366418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215816 | TAACTTCCTGTGTGT[C/G]TGAAGCGTGAAGGGT | 57630 |
| rs150383980 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134201 | GAAAACAGAACAAAC[C/T]GGAATATGGAAGGAG | 57630 |
| rs150403954 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161543 | ATAAAACATTCACTG[A/C]CAATTTATTTTATAG | 57630 |
| rs150446635 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110145 | TTTGGGAGGCCAAGG[C/T]GGCAGGATTGCTTGA | 57630 |
| rs150448564 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191815 | TTTTTCAACAAATGG[A/T]GCTGTGATAATTGGC | 57630 |
| rs150524455 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212925 | GTTTTGCTTTTTCCA[A/G]AATGTAATATAGTTC | 57630 |
| rs150556211 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151986 | TCCAAATTAATAGGG[A/T]TAAAAATCTTTCCTT | 57630 |
| rs150564120 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165700 | TTAGTTTTGTCCAGT[A/G]TTTACATTAACACCT | 57630 |
| rs150566149 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234398 | GAATATGATCTCAGA[C/T]GAAATACCATGGTCT | 57630 |
| rs150585496 | snp | A/C | 1.64876e-05 | 0.00287116 | stop-gained | SH3RF1 | GRCh38.p7 | 4:169269077 | CGGGACATCTGAGTT[A/C]ATTTCGAGAACCTAC | 57630 |
| rs150602547 | in-del | -/GG | | | frameshift-variant | SH3RF1 | GRCh38.p7 | 4:169136424 | TCTCCATGGAGTGGC[-/GG]GGTTCTGGGATGCCT | 57630 |
| rs150607633 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157168 | ATAAAAATCAGAGTT[C/T]GGCTTTTAGGCAAAT | 57630 |
| rs150609613 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188363 | TACTAACAACCACAC[A/G]ATCTTTACATTTCCT | 57630 |
| rs150618075 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269817 | TAAATACATATGTTT[A/C]TTCGCTGTTATTAAA | 57630 |
| rs150651785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142825 | TTTTGCCTCACATTA[C/T]AGTCCTTTGCAAAAT | 57630 |
| rs150670831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262884 | ATCAAGCCTAGCTCA[A/G]GAATGAAGTAAAGGT | 57630 |
| rs150680735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217460 | ATCAAGGCAGGTAAC[A/G]GGAGACAAAATCAAG | 57630 |
| rs150702695 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137116 | ACCATTCAAAATGAA[A/C]TCATGTGCTTCCATG | 57630 |
| rs150713085 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248024 | GAGAAACAGAAATGC[C/T]TTTACACTGTTGGTG | 57630 |
| rs150720363 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132778 | AAACACTGAATATTA[A/T]GAATCACTCCTCTGG | 57630 |
| rs150774644 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207779 | CCCTTTTTCTTAACT[C/G]CTTGTCTACTATGTC | 57630 |
| rs150802880 | in-del | -/AAAACCAACAGCAG | 0.161924 | 0.233971 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109677 | ACCATTATTTTTTCA[-/AAAACCAACAGCAG]AAATGAAAACTAAAT | 57630 |
| rs150816134 | snp | C/G | 3.34091e-05 | 0.00408698 | missense | SH3RF1 | GRCh38.p7 | 4:169116328 | CTGATGAAGCACTGT[C/G]AGGAGATGTGGGGAG | 57630 |
| rs150843446 | in-del | -/C | 0.0189856 | 0.0955633 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261166 | GCTGAAGAAATGAAG[-/C]CCCAGAGAAACCCCA | 57630 |
| rs150860800 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101501 | TACAGATTCAGTTTA[G/T]GATGAGAAAAAGTTC | 57630 |
| rs150916210 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178044 | TGAGGAGTTTGAGAC[A/G]AGCCTGGCCAACATG | 57630 |
| rs150917567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257614 | AAGTAGGGGTTCTCA[C/T]ATCAGTAAAAACTGA | 57630 |
| rs150931823 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272703 | TAAAACTGAAGCTCA[A/G]ATAGGTTAACTTTCC | 57630 |
| rs150936015 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203222 | CTCATAACTCAAAGC[A/G]TCTTGCTCTTTGTAG | 57630 |
| rs150968193 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227350 | ATTCTCTCTTATGTG[C/T]ATTTGAAAAATGTTC | 57630 |
| rs150974616 | in-del | -/GT | 0.395453 | 0.203331 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166113 | AAATTGAAAAATTAG[-/GT]TCAACAACAAAAGAC | 57630 |
| rs150975393 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185494 | AGCATTATTCTTTTC[-/T]TTTTAAGGAAGTATT | 57630 |
| rs151020220 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106247 | CTTCCCAAGTAGCTG[A/G]GATTACAGGGACTCG | 57630 |
| rs151021324 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220760 | AATCTGTTACTATTC[A/C]CTGGTGTGTAATGTA | 57630 |
| rs151027943 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187517 | TTTACAACGAATTTC[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57630 |
| rs151037598 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260359 | CTTTCCTGCTCCCCC[-/T]GTCTGTTCTACCGGC | 57630 |
| rs151039671 | snp | A/G/T | 4.96014e-05 | 0.00497982 | missense, synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116404 | AGAAGCACTGGTGAT[A/G/T]CTTGGGGAAGTCAGT | 57630 |
| rs151074030 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255460 | CCAAAACATGGAAAA[A/T]CTGACCAGTAATAAC | 57630 |
| rs151084199 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211240 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCGG | 57630 |
| rs151090575 | snp | C/T | 0.00243926 | 0.0348379 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169130121 | TGGGCTGCTTGGGGG[C/T]GGGGTCACAATTAAC | 57630 |
| rs151110618 | in-del | -/CCT | | | cds-indel | SH3RF1 | GRCh38.p7 | 4:169122199 | GCAGCGGCGGTGGCG[-/CCT]GGTGGTGTGGAGGCA | 57630 |
| rs151137287 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118523 | GGAGTGGAGTGGTGC[A/G]ATCTCAGCTCACCCC | 57630 |
| rs151157935 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186126 | AGGTTATATAGAAAA[A/G]TTAGTGCAAGTAAAG | 57630 |
| rs151182157 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103306 | GCTTGTTCTCATTAT[A/C]ATCTGTAGATGAATC | 57630 |
| rs151209504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181089 | ACCACATATAAAATT[C/T]GAATGTTCTTAGACA | 57630 |
| rs151231937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260185 | AGTCAGGGGCTTGAA[C/T]TGACATACTGCCCCT | 57630 |
| rs151253459 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173281 | GCTCCTGACCATTCC[C/T]GATTAAGATATTCAG | 57630 |
| rs151284328 | in-del | -/T | 0.391954 | 0.205789 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141640 | GACTGATATAAATAC[-/T]TTTTTTTTTTTTTTG | 57630 |
| rs151304684 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168582 | TGATTGGAACTCGCT[G/T]AATAAAAAAATACAG | 57630 |
| rs180715776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100313 | CTGTCACTATCCTGG[C/T]TGATGACTTCATTAC | 57630 |
| rs180719834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109966 | GCAGTGAGCTATGAC[C/G]ATGCCACTGCACTCC | 57630 |
| rs180721150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128161 | TCATGCAAGGCACTC[A/T]TCTGGAAATGAAAAT | 57630 |
| rs180721546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118617 | CGCGCCACCATGCCC[A/G]GCTACTTTTTTGTAT | 57630 |
| rs180752685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223187 | AGGTAACAGACCCTC[A/C]TCAAGTGCAAGGTGC | 57630 |
| rs180760108 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243470 | GTGAGCCAAGATCGT[C/G]CCACTGCACTCCAGC | 57630 |
| rs180763763 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202338 | GAGGTCAACCTTGAC[C/T]CTCAGCCCTCTCTAT | 57630 |
| rs180769436 | snp | C/T | 0.000807122 | 0.0200726 | missense | SH3RF1 | GRCh38.p7 | 4:169156540 | AAAAAGCCATGGATT[C/T]CATTGACTTCCCCAT | 57630 |
| rs180775917 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186362 | AAGTTAAAAAAAAAA[A/C]GAATTTATTTGGGCA | 57630 |
| rs180775935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139028 | ACATTCATTGCTCAG[G/T]GCAGCCTCGAACTCC | 57630 |
| rs180781057 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176609 | GCACTGGCCTAATCT[C/T]GGCTCACTGCAACCT | 57630 |
| rs180783193 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164205 | AGACCTGGGACTATG[G/T]GTTATGCATCTTTGT | 57630 |
| rs180793780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194636 | AACACTTGAGCTCTT[C/T]CCAGGTGTTAGTTAT | 57630 |
| rs180931381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267290 | AACTAAGATACAGTA[C/T]TCCAGGAAGCCATGC | 57630 |
| rs180949476 | snp | C/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254966 | GGTCAGGAAGAAGAG[C/G]TACAGGGGAGCACCT | 57630 |
| rs180954781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214145 | TTGGGTCATGGGGGC[A/G]CACCTCTTATGAGTA | 57630 |
| rs180982626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234357 | TCTAAAATGTCAAGA[A/G]TGTGAGGTTGGGAAA | 57630 |
| rs181090107 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267792 | AATGGGCAGTTCCTG[C/T]ATTAAATGAAAGACA | 57630 |
| rs181100717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244062 | TCTGATTTAGCAACA[A/G]GCTTCTACATGCTCC | 57630 |
| rs181120461 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223817 | TGATATGTGAGCAGA[A/G]ACTGGATTCAAGTGT | 57630 |
| rs181132476 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203043 | GCATGGAAGGGCTCT[C/G]AGAAGTTCTGCAGCA | 57630 |
| rs181133921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187206 | TATATGTATGTATGT[A/G]CTGACTGATTGAAAC | 57630 |
| rs181142561 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165866 | TGAGAAAAATAAAGT[A/C]TTTTCAAAAGATGAT | 57630 |
| rs181149192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147088 | TGGGGAGAGAGACCA[A/G]TGGATAATTTTTAAA | 57630 |
| rs181152487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175866 | AACCCTAACCAGTGC[A/G]AGAGTATTTGGAGGT | 57630 |
| rs181157395 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155010 | TGCTGGGATGGGATG[A/G]AGGAAGATTCATTGA | 57630 |
| rs181163727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137529 | AAAAAAATTGAGATG[C/T]AAAATAATAAACTTT | 57630 |
| rs181174341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117073 | CCCTCATCCCATTAG[C/T]TACCCAAGACTCTTG | 57630 |
| rs181188718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110537 | TGGGAGGCTGAGGTG[A/G]AAGGATTGCTTGAGT | 57630 |
| rs181211034 | snp | C/G/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128904 | CAACAGCCCTCAACC[C/G/T]AGCCCAAAAAGGAGA | 57630 |
| rs181287725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151152 | TTCAACCAATATTTA[C/T]TGAAAGCGTACTACA | 57630 |
| rs181293917 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133407 | TTGAACCTGGGAGGC[A/G]AAGGTTGCAGTGAGC | 57630 |
| rs181310308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260625 | TCCTCCCTTTCCCTC[A/G]GATTTTCCTTTTCCC | 57630 |
| rs181319412 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219151 | TGATAGACGCAAGCA[C/T]AAGAACAGTGGAAGA | 57630 |
| rs181321080 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240501 | CTTGCATCTGGCCCC[C/T]TTCACTTAATTATTT | 57630 |
| rs181342293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200087 | AGAGTACCTACACAA[C/T]GGTAAATTTAACAGG | 57630 |
| rs181342417 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180801 | ATATAAACAACAAAA[A/C]AAGTAAACCCACCAC | 57630 |
| rs181354678 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161534 | AACAGGTAAATAAAA[C/T]ATTCACTGCCAATTT | 57630 |
| rs181370610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169340 | AGCAGCTCACACCTG[C/T]AATCCCAGCACTTTG | 57630 |
| rs181404927 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095886 | AATCACTAACTTCTC[C/T]TCTCTCAAGTTTCTG | 57630 |
| rs181415569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113343 | CTCAACTCCTGACCT[C/T]AGGTGATACACCAGC | 57630 |
| rs181453738 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227573 | AGCATTTGATATTCT[A/G/T]AAACAACATTTGGCA | 57630 |
| rs181463607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122927 | GGCACAGCCTAATGG[A/G]GTTCTGCCTACAGGA | 57630 |
| rs181466023 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190383 | AATAAGAAACAAAAC[G/T]AGAGACATTACAACT | 57630 |
| rs181483742 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114307 | ATTCCTACCTCTGCT[G/T]CACCATCACGTCTCC | 57630 |
| rs181491557 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104542 | TTAGGGTAATGGCTC[A/G]TTTTAAAACTGGTTT | 57630 |
| rs181520875 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207109 | GCTACAAGTGGGTGC[C/T]ACCATGCCTGGCTAA | 57630 |
| rs181534533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190682 | TATTGACACTATTCC[A/G]CAAGACAGAGAAAGA | 57630 |
| rs181538822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169701 | GGACCACTTAAAAAT[C/T]TTTTATTTAATCAAA | 57630 |
| rs181544584 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151674 | AGTAAGAATAGTTGT[C/T]TATGAGGCCACTCCA | 57630 |
| rs181548707 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133700 | GAGAATTGCTTGAAC[C/T]CAGGAGACGGAGGTT | 57630 |
| rs181577069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248342 | TGTCCTTTGCAGGGA[C/T]ATGGATGAAGCTGAA | 57630 |
| rs181590013 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206824 | CAATGACAAAATGAA[C/T]AGAGAATTATCTATT | 57630 |
| rs181591599 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106168 | CCCAGGCTGGAGTGC[A/G]GCGGCATGATCTCCA | 57630 |
| rs181596017 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261659 | CAATGTGAGTAGATA[C/T]GGAAGCTATCCAAGT | 57630 |
| rs181599760 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144011 | CGAAAGGTTTAGGTT[A/T]GAGTTAGGTCTTTGT | 57630 |
| rs181632246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121714 | TCTCAACAGGATAAA[C/G]TTTTCTGGATACTCA | 57630 |
| rs181637946 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096290 | CTGTGTAGTAAATCA[G/T]ACAGTACAAGGCACA | 57630 |
| rs181671421 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229015 | CTGAAAACAGCTTAA[C/G]CTGATTTATTTTTTT | 57630 |
| rs181689945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143062 | TCCCTCAGGTAACAG[C/T]TCCATTAAGGTCTCT | 57630 |
| rs181763959 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249215 | CCTGGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 57630 |
| rs181773495 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180622 | CCCGCTTGTTTTTTG[C/T]TTTTATTTAATTGGT | 57630 |
| rs181776555 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160886 | CCAAAACAATTGGTT[C/T]GATAGCCTAGGACTA | 57630 |
| rs181780402 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229471 | GGTATACCACCCCCC[A/C]ACCCAAAAAAAAAAC | 57630 |
| rs181784065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143456 | CATTGGATGGCACAG[C/T]TCTAGACTCTCCATA | 57630 |
| rs181793706 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207862 | TTTCTAAAGGGTCCT[C/T]ACAGAAGCAAACCTC | 57630 |
| rs181807316 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104958 | TAATGTAAGTAGGTT[C/T]GAAATTTATTCTTTT | 57630 |
| rs181812660 | snp | A/G | 2.29092e-05 | 0.00338439 | missense | SH3RF1 | GRCh38.p7 | 4:169122229 | GCAAGGACAGTGGCA[A/G]CCAGGAGAGGGGGTG | 57630 |
| rs181814314 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248765 | GTGTTTGTGACTATT[C/T]AGACACAGACAACAA | 57630 |
| rs181814635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099669 | GAAATGGAATAAAAA[C/T]GGTTATTGAAAAACT | 57630 |
| rs181938927 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239881 | ATACAAAAATAAGCC[A/G]GGCGTGGTGGTGTGC | 57630 |
| rs181949864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171676 | ACACCCCAAATCTCA[A/G]AAACTTTATTACCTG | 57630 |
| rs181965423 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134341 | AGCTCTGGTGTGGTA[A/G]CGTCAGGCATGCTCA | 57630 |
| rs182035361 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224389 | ATGGTGCGATCTTGG[C/T]TCACTGCAACCTCCA | 57630 |
| rs182050656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203280 | AACTGGCCAAGCACG[A/G]TGGCTTATGCCTGTA | 57630 |
| rs182050679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254448 | TCAGGTATCCATATG[A/T]TCACAAATATGTATT | 57630 |
| rs182054390 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187509 | ATATTTTCTTTACAA[C/T]GAATTTCTGTGTGTG | 57630 |
| rs182061108 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233902 | CCGCCCCTGCCTCAG[A/G]GCAGCTATAAACCAT | 57630 |
| rs182211248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260040 | TAGATTAATAAATGG[A/G]GTGAGCGTCTGACCA | 57630 |
| rs182223277 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191007 | TGCAGAAAAAGCATT[C/T]GACAAAATCCAGCAT | 57630 |
| rs182234044 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218780 | CTAGGTAGCATCATA[C/T]TCAATAAATACATGA | 57630 |
| rs182240482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151955 | ATGTCATCCAAACTT[A/G]AATGAATGAGTCAGC | 57630 |
| rs182245662 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268505 | TGATAAAATACCAAA[C/T]TTCCATTTTAAAATG | 57630 |
| rs182323161 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117218 | ACGCAATGTCACATG[A/G]ATGGTAGTAGTGAGA | 57630 |
| rs182324470 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193310 | AATGAATGAATGTTA[C/G]CTCCTTTTCCTTTTC | 57630 |
| rs182340912 | snp | A/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155951 | AATGTACATCCTACC[A/G/T]CTTTTCTCCACAAAA | 57630 |
| rs182343734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245944 | AAGACAATCATAAAC[A/T]TCTATGCTCATTCAC | 57630 |
| rs182346635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269695 | CATTGAAAGTTTCCT[C/T]TACCTGAAATTTACT | 57630 |
| rs182348064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224594 | AAGTGCTGGGATTAC[A/G]GGCGTGAACCACCAC | 57630 |
| rs182352397 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198065 | CTTTAAGAAAAATCA[A/C]TTGGTCCAAATTATT | 57630 |
| rs182360516 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179278 | AGGATATTTCTTCTA[C/T]ATAAAAATGTAAATA | 57630 |
| rs182362150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203946 | TTACTTTTTACAAAA[C/T]GGGAATAAACTTTTT | 57630 |
| rs182377368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234669 | TTGGAAACACCCTCA[C/T]ACCATTTCCAATAGA | 57630 |
| rs182380151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214657 | GTTAGCTTTATAGCT[A/G]TAAGTATATAGGTCC | 57630 |
| rs182382509 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195489 | AGTGTTACAAAGTTC[C/T]CAGCCATTTTCTATT | 57630 |
| rs182386784 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177336 | AGACTTCCTCAGCTT[A/G]TACACTAGAGAATCT | 57630 |
| rs182393997 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157894 | TGCAGGCAAGCACCA[C/T]TATGTCTGGCTCATT | 57630 |
| rs182401697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139320 | TGATCTCTGCCCTTA[A/G]GGACCTTACAAACAG | 57630 |
| rs182404001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138233 | TAATGCTTTATATTA[C/T]AGTGGGAGTGGCCTG | 57630 |
| rs182449521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111198 | TCCCACTACTTGGGA[A/G]GCTGAGGTGGGAGGA | 57630 |
| rs182471299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147927 | TGGAAAAATTTAGTG[A/T]GTATATAGCAATAAT | 57630 |
| rs182483178 | snp | A/C | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094469 | CAGATGAAATTTTAA[A/C]CAACTTTATACCAGG | 57630 |
| rs182490640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111847 | CAGATGCCTGTTTAT[C/G]AAACCACGGAGTGCA | 57630 |
| rs182499589 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131140 | CCAGAGGACCTAATG[C/G]AAACTTTCAGTTTCC | 57630 |
| rs182516663 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256015 | TCAAGCAATCCTTCC[A/G]CCTGAGCCATCCAAA | 57630 |
| rs182527511 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097391 | TTGACATTCTCATCT[C/T]TATTATTCTGACATT | 57630 |
| rs182535360 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114635 | TCTGAGACACATTGT[C/G]ATCAAGCCTTAAAAT | 57630 |
| rs182542506 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245017 | CTCGTATTCTGTAAG[C/T]GGATATTCCATCTTA | 57630 |
| rs182570782 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213758 | TACTCCAGCAGCCAT[C/T]TGTTGAAAACACTGT | 57630 |
| rs182575093 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100042 | TGGGCATAACTGGCC[A/G]ACTATTTCAGGCATT | 57630 |
| rs182590878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176093 | CAGGATGAGAACCTT[C/T]ACCAAGAACAGATTC | 57630 |
| rs182603000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257966 | CTGGTGTCAATGGGC[A/C]AATGTGAGAGCCACA | 57630 |
| rs182631088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216862 | CCATTTTTAAAAAGT[A/G]AGTTTGGGCTAGGCG | 57630 |
| rs182650975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187963 | CCATGTGAAAACACA[A/G]AGACATCAGAGTGAA | 57630 |
| rs182684012 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093918 | CGGGTTATCATACTA[C/T]TGGTTGATAGGTCTG | 57630 |
| rs182687648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152334 | AAGAATCCAGGGCCA[C/T]TTATATAGCCATTCT | 57630 |
| rs182694059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134908 | TAGTTGTGCGTTGTG[C/T]GTGTCTTTATTTCTC | 57630 |
| rs182702649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130268 | AAATCTGTACTTTCT[A/G]TTATTTGGGGAAGGT | 57630 |
| rs182773936 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265000 | AGATGCCTCTTCCTC[A/G]GGAAGCTTTTGAAGA | 57630 |
| rs182780442 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221600 | GGCTAAAACGTTCTT[C/T]ATGATAGCACTTCAT | 57630 |
| rs182786955 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241997 | ATTCAGATTTTAAAC[A/C]AAATCTGAAAAGATT | 57630 |
| rs182791355 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201824 | AAAAATCCTGGGGAT[C/G]AGGTCTTAACACAGA | 57630 |
| rs182792060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167924 | GTAGGATATCTTGAG[A/G]CTGGGAGTTCAAGAT | 57630 |
| rs182797249 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135845 | TAAATTAAATGCTTC[A/C/T]TTCTGTCCTTGCTCT | 57630 |
| rs182803527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184106 | ACTCACATGAATGCA[C/T]GGACTGCTCTGAAGG | 57630 |
| rs182888134 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237161 | AAACCAACACCTGAC[A/G]TCTAGTAAGTGGGAA | 57630 |
| rs182916428 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100952 | CCCATACCCTATCAC[G/T]CTCTCAAAGCCTGGC | 57630 |
| rs182918207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251722 | GACCTCACCTATAAG[C/G]AATGCATCAGTGACA | 57630 |
| rs182927033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231349 | AAGGCAGGCAGATCA[C/T]GAGGTCAGGAGTTCG | 57630 |
| rs182939390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209617 | CACTATTAGAAAAGT[A/T]AACAATATAAGTTCA | 57630 |
| rs182944998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192047 | AGATTAAATAGCTGG[A/G]ACTTAATTATACTAA | 57630 |
| rs182945602 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167753 | GGAAATTTCTGAGAC[C/T]ATAAATATATTCTGT | 57630 |
| rs182954019 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174100 | ACAGGGTCTCACTCT[A/G]TCACCCAGGCTAGAG | 57630 |
| rs182961273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152713 | TTGCACTCCAGCCTG[C/T]GCAACAAGAGCGAAA | 57630 |
| rs182984213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246365 | TAATATTTCCACCTC[A/G]GTGTGCTATATAGAT | 57630 |
| rs183041875 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125757 | TCCATTCAGCCCACT[C/T]TCAACCCTACATATC | 57630 |
| rs183072571 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188796 | TCTTCCATACTCCCT[C/G]TATCAATTTGGTGCG | 57630 |
| rs183086819 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148720 | AAGCAAGGAGAGGGG[G/T]TTTTTTTTGGTTCTG | 57630 |
| rs183132839 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230579 | TATCACTGATTCCAC[A/G]TGGGCGCAGTGACTC | 57630 |
| rs183155257 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163234 | AGTATATTCAAACAC[C/T]CAGAAAAAAAAAAAA | 57630 |
| rs183156633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191575 | GAACCAAAAAAGAAC[C/G]AATAAAGCCAAAGCA | 57630 |
| rs183207318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252151 | TTTCACATTTTATAG[C/T]ATGTTGAGTTTTCCA | 57630 |
| rs183215221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201673 | ATTTTGTATTCATAA[C/T]ACCATAATCATTTCC | 57630 |
| rs183219050 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119429 | CACTGCACCCGGCTA[A/T]ACAAGCAGAGAGACT | 57630 |
| rs183221983 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231844 | TCAGGTACTGTTTGA[C/T]ATTAGACATTCAAGG | 57630 |
| rs183226168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181633 | AAATCTGAGGCATCA[C/T]GATGATGATACCTGA | 57630 |
| rs183229153 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162137 | ACTCCAGCCTGGGCA[A/G]TAGAGTGAGACTCCG | 57630 |
| rs183237723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270271 | ACAGGTACTCCCAAG[C/T]CCGCAGGGAGGCGCG | 57630 |
| rs183273260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225253 | TAGTATGACCTGCTT[C/T]GGCTTCAGACATATT | 57630 |
| rs183297903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108399 | TTGTTCCATTAGAGA[C/T]AGTATGGCAGAAAAA | 57630 |
| rs183320849 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115358 | CATCTGTATTTACAG[C/T]CGCTCCCCATCACTT | 57630 |
| rs183322720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107464 | CTTCTCCTCCTTCTC[C/T]CTTTCTGCTATATAT | 57630 |
| rs183330254 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124721 | GTGAAATGATAGGGT[A/T]CTGGTGACTCCAGAG | 57630 |
| rs183343127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144421 | GGAATAGGGTCCTCA[C/G]GTATTCAGTGACCAG | 57630 |
| rs183376012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129886 | GGCAAGGGACTTTCT[A/G]ATGTTTTGTTAAGAT | 57630 |
| rs183394797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257756 | AAGATAATAATCTGG[A/C]AGAACAGAGGTGGAT | 57630 |
| rs183404730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251172 | ACAAGTGGACAGAAG[G/T]TTAGTTAGGAGACTA | 57630 |
| rs183417178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208244 | GTAATAGCCGTTTCT[A/G]TCCAGAGTTTAAATG | 57630 |
| rs183425585 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145738 | CAGGTGTGAGCCACC[A/G]CCTGGTCTAAAAACT | 57630 |
| rs183430437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171863 | AAATTTTAAAAAGAT[C/T]CACTGGATCTAGAGG | 57630 |
| rs183510432 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243682 | ATGCCACAAGGTGAG[A/G]TAATGCCTGAAATTT | 57630 |
| rs183515997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267573 | TTCTCACTATCTTTA[A/C]ATAAATAAATATGTC | 57630 |
| rs183517606 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223399 | TGGTGGCTAAAATGG[C/T]CCTAAAAGGATGGGT | 57630 |
| rs183518254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220397 | CACGCTAGCTTTCCT[C/T]GGTCAAAAATGAAAG | 57630 |
| rs183533524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181112 | CTTAGACATACTATA[C/T]AGTGAGCCGTGCTGA | 57630 |
| rs183545957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123413 | ATTTTTTGCTAAAGC[A/G]ACTTTCAATAAAGAT | 57630 |
| rs183551036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166351 | TGCTGGTGGTAAGGT[G/T]AAAACGGGTAACTTC | 57630 |
| rs183553325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098187 | CGTAACTGGTTACAT[A/G]GCAACAGATATCTAA | 57630 |
| rs183554296 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147498 | TGGGGGAATGGTGAT[C/T]GCCAAGAAAGAATCT | 57630 |
| rs183575853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161846 | AAAGTACCACACAGA[C/G]TAAGAAGTAGAAAAA | 57630 |
| rs183595247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110864 | GTCAGGCGAGACTTA[A/C]AAAGCACCTCTAGAG | 57630 |
| rs183624328 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272794 | TCCAGTTCTCTTTGC[A/G]CCATTCCAAGGCCCT | 57630 |
| rs183632290 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247478 | TATGAAGGTGTGAGC[C/T]AGAGCCTGGAGAAGA | 57630 |
| rs183647657 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226771 | GAAGCTAAAGTCTTA[C/T]AATAACTGTGATTGG | 57630 |
| rs183686429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102034 | TGTTCTCTGTAGTTC[A/C]TACATTTTCATTTCT | 57630 |
| rs183740394 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240716 | TTCTTGTGAGAATAT[G/T]TGAAATCTACTGGCC | 57630 |
| rs183789569 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097091 | TGGGAGAAGTAGCTG[A/C]GCAGGGGGGGTTCAG | 57630 |
| rs183864304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220850 | ATTGTATTAGGTTAG[C/T]ATTTATAATTTCCAA | 57630 |
| rs183865316 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158616 | GAAAATGGACGTGAA[A/G]TGGGCAGGCAGGCAG | 57630 |
| rs183874277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241330 | ATACTGGAAATACAT[A/G]CTAAATACTATTCAG | 57630 |
| rs183874962 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141338 | ATCTTTGCATATCAA[A/C/T]AGGGATAGGCTGATA | 57630 |
| rs183908675 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119649 | TAGAAAAGAATGTTT[A/T]TATTGATTAAAAATT | 57630 |
| rs183974737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159857 | GTTCCTCCTAGGAAG[C/T]GTTCAGGATTTTGAA | 57630 |
| rs184030598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264307 | GTCTGCATCCTCATC[C/T]CCTCTTCTTATAAGA | 57630 |
| rs184034922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236049 | CTGGACAACATTTGC[C/T]TCAGGATCCTTGCCA | 57630 |
| rs184040325 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196550 | ATTTAAACTTGTTCC[C/T]GCCAGATCTTGTGGG | 57630 |
| rs184063433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158320 | AATGAAAGAGAACAG[C/T]AAGGGCATTCCAGGC | 57630 |
| rs184064614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101600 | TGAAAAAATAGTAAA[C/T]TTTCATGTATACTTT | 57630 |
| rs184116142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258978 | ATCCCACACTGACAC[G/T]CTTACTTACATTGCT | 57630 |
| rs184143547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217661 | GCTAGCTGAGCATCA[C/G]ATATGAGGAATAAAA | 57630 |
| rs184145206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237875 | AATTTATGATTTCCC[A/C]CCCGCTCCACACCCT | 57630 |
| rs184149289 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169380 | GGCAGGCGGATCATA[C/T]GAGGTCAGGAGTTCA | 57630 |
| rs184155305 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198495 | TTGCTTTTTATATTA[C/T]GCTAAATATAGTATA | 57630 |
| rs184155427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151176 | TACTACAGGCGCTGT[A/G]CAAAGACCCTGCGGA | 57630 |
| rs184158268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179842 | TTTTCAAAAAGCATC[C/T]TGTCAGAATTATGTA | 57630 |
| rs184182590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216249 | AAAAGAAATAAAGAA[A/T]TAAAAATAAAAGTCT | 57630 |
| rs184202237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178848 | CCAAAATGGGTTGTA[C/T]TCTTGAAAATTACTT | 57630 |
| rs184204239 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232935 | TAAATATCAAGCCTT[C/T]GTATGCAGCAGATTA | 57630 |
| rs184215271 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099376 | TTATAGACATAAGCC[A/G]CTATGCCCAGCTCTC | 57630 |
| rs184219116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140297 | TTCATGTATGAATGT[C/T]TGAGCTCAGTAGTGT | 57630 |
| rs184219702 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116890 | AGTCCCTTTACTTAG[A/G]AGACAGCCTCTCCAC | 57630 |
| rs184281823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175638 | ACAACTTCCTCACCC[C/T]GAACTTTCTACCCTG | 57630 |
| rs184292332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154547 | ATTCCCCAAATAATC[C/T]TGTGCTCTCTCTTAC | 57630 |
| rs184297549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136919 | AACTTGCCAATAACA[A/G]ATGAAAATTTATTTC | 57630 |
| rs184353079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252763 | GTATTCATAAGCAAA[A/C]CACAGGCTCTTTTTT | 57630 |
| rs184392048 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190166 | CACCTCAAGGAACCG[C/G]AGAAACAAGAACAAA | 57630 |
| rs184412215 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150628 | TTTGACCTACGCTAC[C/T]CCCAGGGGGGTCTTC | 57630 |
| rs184426982 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108980 | GAGGCAATAAAGCCT[G/T]TCAATGAGCCTTTCA | 57630 |
| rs184438731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127014 | CTGGTCCAGAGGATC[A/G]GGGATTATTCATCAC | 57630 |
| rs184468254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112884 | TGGCAAGAAGAAAGG[A/G]AAGGATAATCTTCAG | 57630 |
| rs184518006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206003 | AACAATATATTCATA[C/T]TTTTAACTGATAGTT | 57630 |
| rs184528452 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169198 | ACTTCAGGAAAATAT[A/C]TTCTTACTTTGAAAT | 57630 |
| rs184535832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253712 | CTGCATCAAAAGAAG[C/T]CATTATACATGTAAC | 57630 |
| rs184557649 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142052 | CTCAATCTCCTGAGC[C/T]TGTGATCCACCTGCC | 57630 |
| rs184558001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233428 | AAAACTAAAACTATA[C/T]TGAGTATGATTATTC | 57630 |
| rs184561281 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213740 | TGCATTTGAATGTCC[A/G]GTTACTCCAGCAGCC | 57630 |
| rs184563922 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193109 | AAGGCATAAGAATGA[C/T]ACAATGGACTTTGGG | 57630 |
| rs184579492 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175989 | GCCTTTGTAAGAAAA[G/T]ACACAAGAGAGATTC | 57630 |
| rs184583111 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155156 | CTTACTTAAGAACTT[A/T]ATCAACTTTCTACTC | 57630 |
| rs184607176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132988 | AAAGTTCAGCCATCA[C/T]TCAATAGTCACTAAA | 57630 |
| rs184664672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223084 | TCAGTCCTCCAACAC[A/G]CAGACTCACTTTAAG | 57630 |
| rs184680548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202268 | AAACTGTTTCTTTAT[C/T]CTGATGCTTCAGTTT | 57630 |
| rs184685045 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185401 | CAAGTGAGCTGCAGT[C/T]TGAGCTGATCTCTTT | 57630 |
| rs184695373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109752 | CAGTGGCTCACACCT[A/G]TAATTCTAGCACTTT | 57630 |
| rs184696298 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248430 | CTCATAAGTGGGAGT[C/T]GAATAATGAAAACAC | 57630 |
| rs184697513 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163990 | CTATTTCCCAGATGT[G/T]ACAGCCACTACTTGT | 57630 |
| rs184703949 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127409 | AGTACTCACAGTCTT[C/T]GGAACCAATTCAAAT | 57630 |
| rs184707144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206940 | AGTTCAATACTGGCA[C/T]GAACAACATAGTAAG | 57630 |
| rs184728736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104004 | TGAAATGCCATCACC[C/T]GTCTGAGCTAGCAAT | 57630 |
| rs184741423 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112086 | ACAGAGAAAAGGAGG[C/G]GGCAATAGACACGCT | 57630 |
| rs184749453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132048 | CTGCTCCCACACTGG[C/T]GTGTACTTTCATTTT | 57630 |
| rs184757218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104651 | TCATGCCTGTAATCC[C/G]AGCACTTTGAGAGGC | 57630 |
| rs184792671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225637 | AGGTGACTGCAATGT[C/T]AAAGGAAGTGAGTCA | 57630 |
| rs184798622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247057 | AATCAAAAGCAGTTA[A/G]GGCATTAAAAGAGGA | 57630 |
| rs184801628 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205548 | CTGAACTCCAGAGCA[C/G]AGTGCAGCACTGAGC | 57630 |
| rs184815794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189832 | CTCAAGTCTACTACA[C/T]TCAATAAATGTTACC | 57630 |
| rs184819491 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168764 | CAGACTATGACTGAT[A/G]ATCTCTAGTAATCTA | 57630 |
| rs184826227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149572 | TTACTGACTTCTCAA[C/T]AATGTCTTTAAATTT | 57630 |
| rs184846086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227766 | AGTGCCCATCGAAGC[C/T]AGACCCAGTTACTTT | 57630 |
| rs184852109 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190509 | GAGATACAACCCTCC[C/T]AGCTTAATCAGGAAG | 57630 |
| rs184867760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121285 | GCAGTTTCCAAGAGT[A/G]CCTAACTTGCTACCA | 57630 |
| rs184893331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192541 | ACACTGCTGATGGGA[A/C]TGTAAACTAGTACAA | 57630 |
| rs184960913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194798 | TGATTGTATCAATGC[A/G]TGTTCCCTACCAGCT | 57630 |
| rs184962717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176746 | AGGGTTTTACATGTT[G/T]GCTAGGCTGGTCTCG | 57630 |
| rs184996848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212278 | CATGTTGGTCAGGCT[A/G]GTCTTAATCTCCCGA | 57630 |
| rs185051625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239543 | CATCCAAGTTAACTT[A/C]TGAAGAAATAAAAAG | 57630 |
| rs185098257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218830 | GAAAGAAGCATTTAA[C/G]AATAAAAAATGTTAA | 57630 |
| rs185100488 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199904 | ATGTATTTTAAAACA[A/G]TAACAAAATGAAGCA | 57630 |
| rs185112851 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180669 | GCCTACTTAAGTAAA[G/T]AATATTCAGTAAAAG | 57630 |
| rs185121032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161150 | TAAAAGGAGAGAAAG[A/C]CAAAGAGAAACCGAC | 57630 |
| rs185126860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143574 | AGACTGAAATGACTC[C/T]CCTGACTCCCTATGG | 57630 |
| rs185164461 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259591 | CTTTTTAAGGTTACT[A/G]CCTTCAGAAAAAACT | 57630 |
| rs185171528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218523 | TGCCCCCAAAACAAA[A/C]GCAAAACACTGGCCT | 57630 |
| rs185186015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266095 | CTGATGGATTCCCAT[A/G]GTGATTCCAATCCCA | 57630 |
| rs185201419 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105033 | TATGAATGCAGGCCT[C/G]AGGTTTTGGTGGATA | 57630 |
| rs185212063 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122408 | ACAGGGCAGAATCAG[C/G]AGGCTAACTGATATG | 57630 |
| rs185219575 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222326 | AAAAATTAGCCAGGC[A/G]TGGTAGCAGACACCT | 57630 |
| rs185228018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185105 | CTTCCCTATATATTA[A/T]GATAGTTACCTAAAA | 57630 |
| rs185299305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117174 | TTAAGTTAATCAGAA[A/G]TGATCAGCACACCCG | 57630 |
| rs185310705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242259 | ACAAATATAAAACTG[C/T]TTTCACTTGAAAACT | 57630 |
| rs185338825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201962 | ACCCCAGCTCTGACA[A/G]CTATGAGAGAGGAGT | 57630 |
| rs185345568 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137704 | ATCCTGTTGATAAGA[C/T]CACTCTACTAGAAGA | 57630 |
| rs185351364 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163719 | ATTTTCCACCCTCAG[C/T]AAGCAAACCAGTCTG | 57630 |
| rs185372917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174885 | GTCTCCCAGATCTAA[C/T]CTCAGCTATAACCTC | 57630 |
| rs185387064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136063 | AACTGGTAAGTATTA[C/T]ATAACTCATCTTGTA | 57630 |
| rs185391820 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260704 | AGAGAAATATAAATA[A/C]ATAAATAAGGACTGG | 57630 |
| rs185396034 | snp | A/C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219290 | TAATTTATGCCAAAT[A/C/T]GTTTCTGTTCAATCA | 57630 |
| rs185406175 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099849 | ATAAACCTCTGGGGG[G/T]GCGGGTGGAATGAGA | 57630 |
| rs185406953 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200422 | TATAAAAATAAAATC[C/T]CCACAGTTAGAAAAT | 57630 |
| rs185489333 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249455 | TTGATCTTGGACTTC[A/C]CAGTCTCTAGAACTG | 57630 |
| rs185499521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153300 | CAAACTTCTAGGAGA[G/T]AACAGTTTTTGGCAG | 57630 |
| rs185516274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098898 | GTTCAACCTGAAAAT[A/G]TTAGCTCCCATTATG | 57630 |
| rs185517995 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242503 | AATCTCCTGGGAAAC[C/T]TGTTTGAAATGAAAA | 57630 |
| rs185538688 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211476 | AACAGAGCGAGACTC[C/G]GTCTCAAAAAAAAAA | 57630 |
| rs185550661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100750 | CTCAGCCTGGTATGC[A/G]AAGCCCTTGGTGATC | 57630 |
| rs185561262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118839 | GCCAGTGTGAAATAA[C/T]TCTCCTGTATTCATC | 57630 |
| rs185573914 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139048 | CCTCGAACTCCTGGG[C/T]TCAAGCAATCCTCTT | 57630 |
| rs185615023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121882 | AAGAGGCAGTTTCAT[A/G]CCCATATAATATTCT | 57630 |
| rs185628769 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266360 | GCACCACTTGGTTGT[C/G]TCAGAACACTTAAGG | 57630 |
| rs185657077 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115876 | ACTCTTATCAAGCAA[G/T]ACTCACTGAGCAGGA | 57630 |
| rs185657601 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199014 | AATACTTCTAGAAAG[C/G]AGGTCTGAGTTGTAA | 57630 |
| rs185672040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160419 | ATAGACCAGTGGCAA[A/G]GAGAAAGCTTACTAT | 57630 |
| rs185684861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192250 | ATGAATAGACAGTTC[A/G]CAAAAGAAGATATAC | 57630 |
| rs185691639 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096075 | CACTCTATGTCAAAA[C/T]GAATCTCTTGCTCTC | 57630 |
| rs185697395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133456 | CTCCAGCCTGGGAGA[C/T]AACAGCAAAACTCCA | 57630 |
| rs185700904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113354 | ACCTCAGGTGATACA[C/T]CAGCTTTGGCCTCCC | 57630 |
| rs185794757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180175 | CAACCCAGGCTTTAA[A/C]TGATTCTTTCCTTTC | 57630 |
| rs185807703 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234542 | TGATATCCTAATAGC[G/T]GCTTTCATGGGTGAG | 57630 |
| rs185816039 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143275 | ATTTTATTTAGCCCA[A/G]TGTATCTACACTATG | 57630 |
| rs185926366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255252 | CGTGAATATTTTAAC[G/T]ATAAATAGAAACTCC | 57630 |
| rs185948627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214341 | AAGCCAGGCAGATGC[C/T]GGCACCATGCTTCCA | 57630 |
| rs185950187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248881 | GGTTTGAATGGCTCC[A/G]CTCCAAAACTCAGGT | 57630 |
| rs185959792 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229411 | ATGATGTCTTTTTTT[G/T]TGTGTCCCAAATTGT | 57630 |
| rs185968145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191145 | AAAGTTGAAATAATT[C/T]CCTCTGAGAACTGGA | 57630 |
| rs185973783 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207252 | AGCCTGGCCAAAAGA[C/T]GCCACCTCTACAAAA | 57630 |
| rs185980406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186478 | TTTCTGATTCCATTA[C/T]AAAACATCCTGTTCC | 57630 |
| rs185981327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152236 | GAGAGGTCTGAAAGA[A/C]TCTCCGGAGGGGAAG | 57630 |
| rs185986350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144612 | GAGGCACAAATTCAC[A/G]TGTCTGCATAGCTTG | 57630 |
| rs185988271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190690 | CTATTCCGCAAGACA[A/G]AGAAAGAGGGAACCC | 57630 |
| rs185990381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170443 | AGAAAATTAATAATC[A/G]GAATACTTTTGGTCA | 57630 |
| rs185996168 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123883 | GGTGACAGAGCAAGA[C/T]TCCGTCTCAAAAAAA | 57630 |
| rs186026231 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256668 | GTGACAAGATCACAG[C/G]TCACTGCAGCCTCAA | 57630 |
| rs186042718 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215411 | ATTGCAGTTCCTTTT[C/G]TTGTAATGTCTTTAT | 57630 |
| rs186046818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235473 | TATTATTTCCATTTA[A/T]ATATGAGCCAACTGA | 57630 |
| rs186058861 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196361 | CATTGAACAAAACAA[A/T]GTTATTCAAGGACCT | 57630 |
| rs186063025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100054 | GCCAACTATTTCAGG[C/T]ATTGAAAGGCTTTGC | 57630 |
| rs186096528 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240220 | CTTTTTTTTTGAGAC[A/G]GGGTCTCACTCTGGC | 57630 |
| rs186102870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171710 | CTTTCAAGTGAAAAC[C/T]ATAACAATTATGCAA | 57630 |
| rs186109107 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114529 | TCACTATTCTGTCTA[A/T]CACAAGTACCTTTCA | 57630 |
| rs186118665 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134535 | AACATCATTGTGCAA[A/T]TGTTGCTAGGTCCCA | 57630 |
| rs186128473 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147363 | GTGAAAATTTGTCAA[C/T]GTGAAATGACACACT | 57630 |
| rs186146332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260243 | TTTTATTCTTTTGCT[C/T]TTCTGAGACCAGAGA | 57630 |
| rs186148360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229763 | CCCACTTTATGCTCC[C/T]GAGAGTATACGACGG | 57630 |
| rs186166840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106388 | CCAAGACAATTCTTC[C/T]TTCAGTGTGGCCCAG | 57630 |
| rs186233879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097130 | GAACCGCCTGCCCAC[A/G]GGCTAAGGAGGCTCT | 57630 |
| rs186237569 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110736 | GACACTAAATGTTGA[C/T]CTTATGTGGCCCACC | 57630 |
| rs186260215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251579 | CTGAGGTTGGCTTTC[A/G]TCCTTCAAAAGCTTT | 57630 |
| rs186285060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207886 | AAACCTCTCCCCACA[A/G]AGCTGGACTCAGATC | 57630 |
| rs186301150 | snp | A/G | 1.7105e-05 | 0.00292441 | missense | SH3RF1 | GRCh38.p7 | 4:169130077 | TAGGGAACATCTGAT[A/G]GGAAAGTAAACGAGG | 57630 |
| rs186310799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180963 | TCACCTGCCAGCAAC[C/T]CTTTCTTTTCTCTTT | 57630 |
| rs186321688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123239 | ACCAGTCATCTTATT[C/T]CTGTTTTTTGGAATA | 57630 |
| rs186321878 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144378 | ATATCCCATTCAAAA[C/T]ATTCAATAGGCAAAG | 57630 |
| rs186370251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224471 | TACAGGCTCGCGCCA[C/T]CATGCCTGGCTAATT | 57630 |
| rs186376238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245455 | AATTTATCTATATAG[C/T]CCACTAAAATCTACT | 57630 |
| rs186389038 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254676 | GTGAGTTATTTTTAA[A/G]GGTACATAACATGAG | 57630 |
| rs186389727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203740 | AAAATAACTGTGAAA[C/T]GAATGACTGAATAAT | 57630 |
| rs186392706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187810 | TTGTCCATCCCCCTG[C/T]AAATTCATATCTAGC | 57630 |
| rs186397137 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166902 | CTCAAAACATCTTAC[C/T]GTTGCTTACTTCAAG | 57630 |
| rs186402854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147815 | CATGCTGGACCAGTA[G/T]AGAATATTCATTCAG | 57630 |
| rs186476183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165164 | GGTCAAGTTTCTACC[C/T]ATTTGAAAAACAGAT | 57630 |
| rs186491244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161634 | CATGCATTTCTTACT[A/G]CTCCATAAAGTAAAA | 57630 |
| rs186521351 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151779 | TGAAAAACTGAGTGG[A/G]CGATATTTCAAACAA | 57630 |
| rs186526446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134084 | AGTGCCCTAGATAAG[C/T]AGTGTTTTCTGTAAA | 57630 |
| rs186579475 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240987 | TGTAATCCCAGCACT[G/T]TGGGAGGCTGAGGTG | 57630 |
| rs186607900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200799 | CCAGAGTAGTCTGGT[A/G]AGACAGGTATATCAG | 57630 |
| rs186620595 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110160 | CGGCAGGATTGCTTG[A/G]GCCCAGGAGTTGAGA | 57630 |
| rs186625765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246211 | TATTTCAGAATATTT[C/G]AAATAAGACTCAGCT | 57630 |
| rs186631191 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217233 | ATAGTCAGACAAGGC[C/T]TGGTTCAACACCCTG | 57630 |
| rs186631377 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269771 | AGAAACCATGCCTCA[A/T]GTAATCGCTCGTGGT | 57630 |
| rs186631429 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162071 | GTCCCAACTACTTGC[A/G]AGGCTGAGGCAGTAG | 57630 |
| rs186641795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179311 | GAAACATTTTGTCCT[C/T]AGAGCCACCAAAAAG | 57630 |
| rs186641976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224777 | GATGTAATAAGATGA[A/G]GGAGATCTTGAAGAC | 57630 |
| rs186653769 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158972 | TTGTAGTTGGTTAAT[C/T]AGAACTTCCCTGAGA | 57630 |
| rs186659562 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141731 | CAACCTCTGCCTCCC[C/T]GATTCAAGTGATTCT | 57630 |
| rs186692852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146409 | TTATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 57630 |
| rs186718067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102223 | CCCTTTGTAGCTTGC[A/T]CCAAGTCCAAGTAAA | 57630 |
| rs186725800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121045 | GACAAATCCCAAGAT[C/G]CTCAAAATTCTTCCT | 57630 |
| rs186764668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223941 | AGTGTAGCTGGAAGA[A/T]AATACGTGAATCAAA | 57630 |
| rs186778646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187232 | GAAACAGGGTCTCAC[C/T]GTGTCACCCAGGCTA | 57630 |
| rs186795092 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262291 | ACTTAATAACATATT[A/C]TTCTATATGGTTGAA | 57630 |
| rs186798005 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162664 | GAAATTAAGACAAAA[C/T]GTTGTTTCTTCATTC | 57630 |
| rs186803095 | snp | A/T | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145564 | CCCCGAATCTGTAAA[A/T]ATATATATATATTAT | 57630 |
| rs186827570 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151482 | GGAATCCTGGCCATC[C/T]GGCTCCAGAGTCCAA | 57630 |
| rs186835960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220416 | CAAAAATGAAAGAAC[C/T]GAATGAACTTCTGTT | 57630 |
| rs186852799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097633 | GCATTATTTGCATTA[C/T]TCCTCTTCTCAACAA | 57630 |
| rs186859920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114831 | AAGTTTATTTCCTTA[C/T]AAACTGCTGTTTACA | 57630 |
| rs186942645 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191873 | ATCCTCACCTCTCAC[C/T]TTATACACAAATCAA | 57630 |
| rs186946917 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172100 | TGGGAGGTAGAAGTA[C/G]TCTAAATTTTCCACT | 57630 |
| rs186954950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268231 | AAGCCCAACATAAAG[A/C]TAGATGTTTTAGTGT | 57630 |
| rs186956284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152519 | GAGGCAGGCGGATCA[C/T]CTAAGGTCAGGAGTT | 57630 |
| rs186957866 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107778 | GAGTTAAGAGCTAAA[A/C]CACTTCTCACATGTC | 57630 |
| rs186957919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241380 | TCTTCAGCAAACTCA[A/C]CCTTCAGCCGAAAGG | 57630 |
| rs186965451 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135462 | CTTCTGCTTGTGACA[C/G]GCAGCTTTGAACTAG | 57630 |
| rs186965879 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221009 | GGTCTTTGAACTCTC[A/G]TGTCGAAAGAGTTGA | 57630 |
| rs186969956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201747 | CTCCTGAGGCTCTGA[C/T]TTCCCAGTTGAAATC | 57630 |
| rs186973960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181842 | TCTGTTATTTATGTG[C/T]CCACCACTATGTAAA | 57630 |
| rs186974186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099117 | ATCTTTATTTTGAGA[C/T]GGTCTTACTTTGTTG | 57630 |
| rs186976137 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203122 | ATTATTTGACCAAAC[A/G]TCTCACAGAAAACAC | 57630 |
| rs186978628 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115903 | AGGAAGACTTGAGGA[C/G]AGCAAAATGATGAAA | 57630 |
| rs186999572 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166048 | TAGTGATGTGTAGGG[A/C]GGGGAAAAAAGCCTA | 57630 |
| rs187001487 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110964 | TTTTCTAAAGCAAGG[G/T]TTAGAACTTAGAGAA | 57630 |
| rs187141380 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213773 | TTGTTGAAAACACTG[C/T]CTTTTCTCCATTCTA | 57630 |
| rs187156641 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176446 | TTTTAGAATATTTTC[A/G]TGGGTGATCAATTTT | 57630 |
| rs187167233 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138394 | AACACAACATCCTCA[C/T]GAAATGAAGGGCCAG | 57630 |
| rs187168984 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244150 | GTTGCTGTTCTAATA[C/T]GTTTTAAGACATTTA | 57630 |
| rs187199623 | snp | C/T | 6.59359e-05 | 0.00574139 | missense | SH3RF1 | GRCh38.p7 | 4:169117540 | GTCCTCACAGCATTG[C/T]GGGCCTGGTTGACTG | 57630 |
| rs187218662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251910 | ACATTAAAGAAAAGC[C/T]TTGCATATTCATCAA | 57630 |
| rs187230228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231686 | AGAATACTCACTCCT[C/G]CATCCAACATAACCA | 57630 |
| rs187240256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209937 | TGGGACTACAGGCAC[A/G]CATCACCACACCCAG | 57630 |
| rs187241850 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192116 | AACAGACAACCCACA[C/G]AGTGGGAGAAAATCT | 57630 |
| rs187245791 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242093 | GAGGGATCTATAAAT[G/T]CTTAATCAAATATTT | 57630 |
| rs187252400 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265867 | AATCATTGGAACTGC[A/G]CATAAAAAGCAGAAA | 57630 |
| rs187253231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174108 | TCACTCTGTCACCCA[A/G]GCTAGAGTGCAGTGG | 57630 |
| rs187253338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221606 | AACGTTCTTTATGAT[A/G]GCACTTCATTTTAAC | 57630 |
| rs187271912 | snp | A/G | 5.03613e-05 | 0.00501778 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096512 | AGCTTCTTCAGTGTC[A/G]GTCTCCTCATATGTT | 57630 |
| rs187278087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269473 | TCCAAAGTCAACAAC[C/T]GAAAACAAAACAGGC | 57630 |
| rs187333470 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233939 | TCCCTGTTAGTTACC[A/T]TCTGCTTCCCCATCC | 57630 |
| rs187338920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193650 | ATTACAGTGCAGGTC[A/C]TGTCAGGGAACACAT | 57630 |
| rs187364978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177763 | TTTCCATAAAGTTTA[C/G]AGGTTAAAAGATAGA | 57630 |
| rs187365389 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156030 | ATATATTCCTGTATG[C/T]TTTTAGGCAAAGAAT | 57630 |
| rs187449317 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237292 | ATTATTTTCAAAAGC[A/T]TTAATTTTCCAAAGG | 57630 |
| rs187481199 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204332 | TTTCATTCAATCATC[C/G]TATTCTCTGTCAAAG | 57630 |
| rs187494326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167792 | GGAGGTGTTAGTTAT[C/T]CTGGTGTAGAAAGGT | 57630 |
| rs187502812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114316 | TCTGCTTCACCATCA[C/T]GTCTCCTTCTCTGGC | 57630 |
| rs187522600 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094480 | TTAACCAACTTTATA[A/C]CAGGAAACTATGAAC | 57630 |
| rs187528810 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111900 | TTTAACACAAGGACA[A/T]AAATGCAATGTCTAG | 57630 |
| rs187530539 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168153 | TCTAAAAACAAAAAC[A/G]AAAGCAAAAGTATCA | 57630 |
| rs187530891 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130434 | GCTTTCACGGTAACA[C/T]ATTGCCTCATTTGGT | 57630 |
| rs187533726 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131239 | AATCTATGCTATACA[C/T]GGAATCTGCAATCTT | 57630 |
| rs187536864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148870 | TGAGCTGTAAAGAGA[A/G]CAGTTCCAGGGTATG | 57630 |
| rs187651594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190074 | GGGACACAGCAAAAG[A/G]CAGTGCCAAGAGGAA | 57630 |
| rs187658282 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168851 | TCCTTTGTTTCTTAG[G/T]GGTGGAATCTCAATA | 57630 |
| rs187688244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258655 | GAAAAAACTGTTCAA[A/C]GATTTTGAAAAAAAC | 57630 |
| rs187725502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101907 | GTCTTGCAATATAAA[A/G]AAGCTCCACAGACTT | 57630 |
| rs187730350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264646 | CACAAGCTCCAATCC[C/T]GTATCTGTTCTGAAG | 57630 |
| rs187732362 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232206 | GGCTCTTGGAGACAG[G/T]GCCAAAATTTTTGGA | 57630 |
| rs187734908 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188102 | CTAGAGCCTTCAGAG[A/G]GTGCATGGCCCTGCT | 57630 |
| rs187736944 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119807 | TTGTTTAAAATCAGG[C/T]GGTTTGAGGAAAGAT | 57630 |
| rs187743437 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192331 | GGAAATGCAAACATG[A/C]ATAGACAGTTCGCAA | 57630 |
| rs187750646 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148325 | GAGCAAGACATTTGT[C/T]TACAAAATGGTAAAA | 57630 |
| rs187771605 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153907 | CTTGAAGTGACTCTG[G/T]ATTTGCCATGGGTGG | 57630 |
| rs187772151 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111538 | CCAAACTTTTGGGAT[A/T]ATAGGTGTGAGCCAC | 57630 |
| rs187822219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247211 | AAGAAGAGGCAAACC[A/G]AAAGGGAAGAGGTGG | 57630 |
| rs187824253 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272200 | GAAATCTCTGCCCAG[C/T]CACCAACTAGGTTTA | 57630 |
| rs187832331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226109 | CTTAATGTCGTGACA[A/T]CAGAACAACCAAATG | 57630 |
| rs187834858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108631 | ACCCTGCAACTCTCC[C/T]GGGTAGAGGAAGATC | 57630 |
| rs187838935 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247885 | CAGCCAACAAACATG[A/C]AAAAAAGCACATCAT | 57630 |
| rs187844618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205670 | TCTGGAAGGAGCCCA[A/G]TGAATGACGTTAGCA | 57630 |
| rs187897380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184715 | GAAAGTTTTGTTTTG[C/G]GGTATTTATTTATTT | 57630 |
| rs187965933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161466 | TTTCCATACCATCAG[C/T]GGTATTCCAATACAT | 57630 |
| rs187975374 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143997 | CCTGAACTTCACACC[A/G]AAAGGTTTAGGTTAG | 57630 |
| rs187982946 | snp | C/T | 0.000203108 | 0.0100753 | missense | SH3RF1 | GRCh38.p7 | 4:169107153 | GGAGACACGCGGGGC[C/T]TCCGTTTAGTGGAGG | 57630 |
| rs188015727 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252356 | TTCCCCAAGGTAATG[G/T]GTCAAAAATTTACTT | 57630 |
| rs188024346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211589 | AATAGCACTTGTCTA[C/T]TATGAATAAGGGACG | 57630 |
| rs188041790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175048 | CCCAATGTTGGTAAA[G/T]AGCCCACTGTTCACC | 57630 |
| rs188059716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136677 | ATTCCTAAGAATTCC[C/T]TGAGGTTTATTTCCA | 57630 |
| rs188073807 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094026 | TGCCATACATGACCT[C/T]GTGCGACTCCACAAA | 57630 |
| rs188118233 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260320 | CCAGAGAAGCAGTTT[C/T]AGGAAGGCAATGGAG | 57630 |
| rs188125737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126143 | ATGATTAATGAGATT[A/G]TGAAGTCAGGGACTG | 57630 |
| rs188130422 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273040 | ATCAATAGTCACACC[C/T]ATTTTCTTTTCTTTT | 57630 |
| rs188141278 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240255 | AGGCTGGAGTGCAGT[G/T]GTGCAATCTCAGCTC | 57630 |
| rs188145700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248259 | CCCATTAATGATAGA[A/C]CGCATAAAGAAAATG | 57630 |
| rs188149182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218881 | AAATTTTGCTTTAAG[C/T]AATTAGGAGTCAATG | 57630 |
| rs188153759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199951 | AGGCACACCTAAAAC[A/G]TAAAGACATAAAAGA | 57630 |
| rs188167684 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201851 | CAGAAAACCCATCTG[C/T]CGTCGCTACAGAGGC | 57630 |
| rs188167876 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230756 | CCCAGCTACTCAGGA[A/G]GCTGAAGGAGAATCA | 57630 |
| rs188183891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163529 | ACTAGAGAGGTAGGA[C/T]GAAAACCAGCAAACT | 57630 |
| rs188224101 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095691 | CCCTACTTTCCAACC[A/G]AACAATTGAGCTGCT | 57630 |
| rs188250935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135937 | AACTACAAACGTCAC[A/G]AGTTTGGACCATGGC | 57630 |
| rs188273268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267089 | CCAAATAATTTACCT[A/G]TGAAGTTCAATTTTG | 57630 |
| rs188281017 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223128 | ACCTTCCTGGGGCCT[C/T]TCTGCCAGGAAGATA | 57630 |
| rs188282984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242899 | ATTTCTATCATTATA[A/G]ATCACCCAGCCTGTT | 57630 |
| rs188285550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098513 | CACTAAAAAAACACA[C/T]CTCTGCAAAAGGTAA | 57630 |
| rs188300658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202308 | CTCCCTCCGTAGGAG[A/G]CTAGTTCTTGGTATG | 57630 |
| rs188306402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185944 | TGTCATAAGCTTATT[C/T]GCACATACCTTCACC | 57630 |
| rs188310454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164141 | TATCATGGCCCTTAT[C/G]TTACTCAGTTTATAA | 57630 |
| rs188322050 | snp | C/T | 0.304688 | 0.243945 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146028 | CTATATAAAATATTA[C/T]ATATTCTATATATTC | 57630 |
| rs188391989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157999 | CCACCTTGGCCTCCC[A/G]AAGTGCTGGGATTAT | 57630 |
| rs188483197 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222487 | ACATATATATGTATT[A/T]TATATATATATTTTT | 57630 |
| rs188518439 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271251 | GGGATTGGGGCGGCG[A/G]CCTGAGGGGGCGCTG | 57630 |
| rs188529873 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152926 | TCAATCCTCTCTTTA[C/T]CCACCTCCAGTGCTC | 57630 |
| rs188544378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225540 | ACAGATGTAAAGGAG[A/G]GTAAACTGGGTAAAA | 57630 |
| rs188545966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099515 | AGCAATGATGTAGTT[A/G]CCATGTGGGGCAAGT | 57630 |
| rs188546131 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119441 | CTATACAAGCAGAGA[G/T]ACTTCTAATAATTGG | 57630 |
| rs188552666 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189414 | GGTAGGTTAGCATGA[A/G]TTTTCTTACTCCTCA | 57630 |
| rs188554246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116900 | CTTAGGAGACAGCCT[C/T]TCCACAGTGTTAGAG | 57630 |
| rs188576183 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115494 | ACACTCCTTATGAGA[A/C]TCTAATGCCTGAGGA | 57630 |
| rs188582785 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154639 | TCCATGTCTCTTAGT[C/T]AACCCTTATTTATCC | 57630 |
| rs188587161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244011 | CAACAGACTAAAGAG[C/T]AGTAAATGAGGTTTT | 57630 |
| rs188591399 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267782 | ATGCTATCCCAATGG[C/G]CAGTTCCTGTATTAA | 57630 |
| rs188592914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137367 | AAATCTGTGCACTCC[A/C]CTGATATTATCAGCA | 57630 |
| rs188647731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266260 | TGGTCACAGCCTAAC[C/T]AAACACAGAACATAA | 57630 |
| rs188682164 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139812 | CCATTACCTAACTTT[A/G]GGGCCTTAAGGGAGC | 57630 |
| rs188687388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216350 | TTTAAGCATTTAAAA[A/C]TTTTCATTATTTGTC | 57630 |
| rs188697647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178916 | TATTTTTCACTGATA[C/G]CTTAATACAAATGTA | 57630 |
| rs188718137 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140518 | TAAAATTCTTATGCC[C/T]CTTTTTGGAAAAAAG | 57630 |
| rs188751817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213340 | GAAGTGTCTGTTCAG[A/G]TCTTTTGCCCATTTT | 57630 |
| rs188766223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192815 | ATATATATGATATAT[A/G]TGTGATATATATATC | 57630 |
| rs188770068 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175752 | GTTCAACAGAGAATC[A/C]CAGGCCTATATCCAT | 57630 |
| rs188786335 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163798 | TCATCGAGAACAGTC[C/T]ATTTCTCCCTCCACC | 57630 |
| rs188819388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100957 | ACCCTATCACTCTCT[C/T]AAAGCCTGGCTCCAG | 57630 |
| rs188819435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246466 | TCTGCTCCACAGACA[C/T]TGAAGAGGTCATGCT | 57630 |
| rs188829587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204846 | GAGCCACTGAGCCCC[A/G]GCCACCTTCTCCTTT | 57630 |
| rs188870685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257796 | AGATGAGATCTAGCA[A/C]GCAAACCAGCCCTAT | 57630 |
| rs188875849 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109319 | AATATCAGATAACTC[A/C]ACGGCACTCAGGGAA | 57630 |
| rs188881231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127079 | ATACGAGACTAAGAT[C/T]TTCAACCTCCTCCCC | 57630 |
| rs188884378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193246 | TAAAGAACTCACTTA[C/T]GTAACCAAACACCAT | 57630 |
| rs188969796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197130 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 57630 |
| rs188979379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206643 | TGCTACAAAGATAAA[G/T]TATACAGAGAATCCC | 57630 |
| rs188985860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158574 | TTAGGTCCTATGTGC[C/T]GGACAGATCAGTCTG | 57630 |
| rs189004199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169301 | TAAGTCTTTTCATTA[A/C]AAAAATAACAAGAGA | 57630 |
| rs189067346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213742 | CATTTGAATGTCCAG[A/T]TACTCCAGCAGCCAT | 57630 |
| rs189069838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233870 | AGGGTCTTCCTTCCC[C/T]CACGATTTCTCTATT | 57630 |
| rs189084726 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096076 | ACTCTATGTCAAAAC[A/G]AATCTCTTGCTCTCA | 57630 |
| rs189097496 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114202 | GGGCTGGTTCCTTCT[C/G]GAGGCCACTGGGGAA | 57630 |
| rs189125075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133132 | GGACCCACTTATATG[A/G]TGTAGACATGAGCTG | 57630 |
| rs189149001 | snp | A/C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236383 | AATGACTATAATGAG[A/C/T]GGTGTCCCTCTGCCA | 57630 |
| rs189194304 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128146 | CAAGTTAGAATTTTA[C/T]CATGCAAGGCACTCA | 57630 |
| rs189207547 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190568 | AAGCAGAGAGACTGA[A/C]ATGGTCATTTTAAAA | 57630 |
| rs189209365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104838 | CCCGGGAAATGGAGG[C/T]TGCAGTGAGCCAAGA | 57630 |
| rs189209830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217943 | CAATTTCCCTGAGAA[C/T]ATTCCTATGGTTTTC | 57630 |
| rs189213540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238411 | TTGAGCTGCCACAGA[C/T]ACTCTGCTGCCCTCT | 57630 |
| rs189215807 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169561 | GAGACTGCACCACTG[C/T]ACTCCAGCCTGGGCA | 57630 |
| rs189218514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121950 | TTCCCTAGTTACATG[A/C]ATGACCAGGTAGAAG | 57630 |
| rs189228393 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151656 | TTCTAGCAGTAACTA[C/T]TGAGTAAGAATAGTT | 57630 |
| rs189230620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143372 | CTTTGAAACCCGGTG[C/T]GAACGGAGTGCTTCC | 57630 |
| rs189231083 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198633 | CTAATTTGTATAAAT[C/T]TTTACACATGTATAC | 57630 |
| rs189244957 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149790 | TGCTATCTTTTTATA[C/T]AGTTCAATCAACTCT | 57630 |
| rs189268814 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227506 | GAGTTGGAATTTATG[C/T]TTTAGAACTTGTAAT | 57630 |
| rs189277996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234178 | CTGCCAGGAACGTGT[A/G]ACAATGTCAATTTTT | 57630 |
| rs189283670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190314 | GATAAATCAAATTGA[C/T]AGACCATTAGCAAGA | 57630 |
| rs189296167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151036 | TAGGCAGTGAATGAT[A/G]GGAGAATTAGCTGAA | 57630 |
| rs189298353 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194564 | TTTATTACTTTTCAT[G/T]GAAGCATACTATTCC | 57630 |
| rs189402612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113247 | TCCTGAGTAGCTGGG[A/T]TTACAGGCATGTGCC | 57630 |
| rs189465011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110489 | AGAATAATAAGCCAG[A/G]TGCCGTGGTGTGAAC | 57630 |
| rs189466285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109906 | CCCATCTACTCCGGA[A/G]CCTGAGGTGGGAGGG | 57630 |
| rs189561989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254910 | CAGTTATTCAGTCCA[A/G]ATAAAAAGAGAGGAG | 57630 |
| rs189580491 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214121 | GAGGTGGGGCCTCGA[A/G]GGAAGTGTTTGGGTC | 57630 |
| rs189635303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253437 | AGCTAGAGAGCCCAT[G/T]GGCTTTTGTCATGTT | 57630 |
| rs189643624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223503 | CAGGGAAGAGACATC[C/T]GCTCACTCATTCAGA | 57630 |
| rs189652473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187019 | CTCCATCGCAAAAAA[A/G]AAAAAATGAAAAAGA | 57630 |
| rs189673365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146521 | GTGTGAGCCACCACC[C/T]GGCCTAAAAAATATA | 57630 |
| rs189684820 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122748 | AAATTTCCTTTGATG[C/T]CTGGTCTACAAAAAG | 57630 |
| rs189692244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097244 | GGTGTTTGACATGGG[C/T]GAGGCAGCAATTCTG | 57630 |
| rs189696670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114581 | TCTACATTGGAAGGG[A/C]CCAGCTGAAGAGTCC | 57630 |
| rs189737603 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100252 | TACATGGGACCTGCT[G/T]ATCTACCTTCAAAAT | 57630 |
| rs189750199 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117987 | AATATATTCTGAGTC[A/C]CCAGAAACCACACGT | 57630 |
| rs189780659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264989 | GATCTCAGCTCAGAT[A/G]CCTCTTCCTCAGGAA | 57630 |
| rs189792464 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241756 | ACTTGACCTTGCAGC[A/G]TGGTTACTGAGATAC | 57630 |
| rs189806327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176087 | GCAAGCCAGGATGAG[A/T]ACCTTCACCAAGAAC | 57630 |
| rs189810590 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202144 | ACCTCAGGATATAGA[C/T]ACTGAGTTGCAATGG | 57630 |
| rs189826808 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137999 | AATAATAGGCAGTAA[C/T]GCCAGAATAACACCT | 57630 |
| rs189868144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138968 | ATTTTTGGGGGGACT[A/G]GGGGGAAAGGTCTCA | 57630 |
| rs189910251 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232993 | GTGGCTCACACCTGT[A/C]ATCCCAGAACTTTGG | 57630 |
| rs189910472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203000 | ATTTGGGATAGACAG[C/G]TCTTGGAGAAAAAAA | 57630 |
| rs189928777 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165640 | GAGAAAAAAAGGCGG[C/G/T]GGGGGGAGTCAGGTA | 57630 |
| rs189936840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099904 | GACACAGTCTTGATC[A/G]TATGAAGACTACCAG | 57630 |
| rs189945520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128709 | TTTGACTAATTATGT[C/T]GTGGAGTCTTTGCTG | 57630 |
| rs189949105 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203792 | TCTTCCATACTCCCT[A/G]CAAGATACTAGAGAT | 57630 |
| rs189964664 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187872 | AGGGTCTAGGGTCTT[C/T]GCAGATGGAATCCGC | 57630 |
| rs189972362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167073 | TACCTATAATCTGTG[A/T]TTGCCCTGACAAATA | 57630 |
| rs189997030 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121519 | TCAAGGGAGAACAAA[C/G]TCCAGATCACAAAAC | 57630 |
| rs189999453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209270 | CTCCAGCCTGAGTGA[C/T]AGAACAAGACCCTGT | 57630 |
| rs190001632 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240560 | TTAAAGATACCAACG[G/T]GTATTAAGGAGTTTT | 57630 |
| rs190003709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260927 | TCTCATCATCCCAAA[C/T]AGAAATGAAATTAAA | 57630 |
| rs190071547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155852 | TTGCAACCTCAAATG[A/T]TACCTACCCTAGCCT | 57630 |
| rs190079782 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185150 | ATTTTGTTCAATCAT[C/G]CCACAAATATTTATT | 57630 |
| rs190106229 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227936 | AATGAAGGGAACTCT[A/G]CAAATCACAGTCATG | 57630 |
| rs190130920 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234656 | TGCCTGGCATTGTTT[A/G]GAAACACCCTCATAC | 57630 |
| rs190144749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214342 | AGCCAGGCAGATGCC[A/G]GCACCATGCTTCCAG | 57630 |
| rs190148666 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195153 | AAAATGTCTTTATTT[A/C]ACTCTCATACTTGAA | 57630 |
| rs190160559 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160324 | ACAGATCACTTCCAC[A/T]CACCAGTGGCCTAAT | 57630 |
| rs190171401 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157402 | GAGCACATTGTTAGG[C/T]TGATAAGCTAAGAGA | 57630 |
| rs190179365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139153 | TCATTATGATATCTA[A/G]CTGGTGTCGAACTTC | 57630 |
| rs190198077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117204 | GTTAGTAGAGTATCA[C/T]GCAATGTCACATGGA | 57630 |
| rs190219128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119055 | ATTATTTACCATGAA[C/T]GACAGAATTTACTGT | 57630 |
| rs190252394 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112468 | AGAACTGATTTTTAA[A/G]TGTTCAAAGAAAATA | 57630 |
| rs190356459 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248624 | CAAACCTGCACATTC[C/T]GTACATGTATCCCAG | 57630 |
| rs190374562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207043 | AGCTCACTGCAGCCT[C/T]GATCTCCCAGGCTCA | 57630 |
| rs190405394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180043 | AACTTTGGCCACATC[C/T]ACTGCATGGGGACGT | 57630 |
| rs190418618 | snp | A/G | 0.00119832 | 0.0244484 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142128 | TGGCCTTAATTTGCA[A/G]TTTTTTTAGTAGAGA | 57630 |
| rs190431602 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104042 | TTTCAGATGAACTGA[A/C]CAGCAGGAGCCTGCT | 57630 |
| rs190432924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270128 | CCCCCACCGCCAAAA[C/T]AAATGTAAAAGTGAA | 57630 |
| rs190444661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166326 | AGGAACCCGAAGCCA[C/T]GAAGGCTGATGCTGG | 57630 |
| rs190446343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260005 | CTTAAACTACATTAA[G/T]CAATATACTAGAGAG | 57630 |
| rs190452868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147458 | TGGATACTTAAAGCA[C/T]GTGTGGATGTGCATG | 57630 |
| rs190457606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215475 | ACAGTAAGTTACAAA[C/G]TATTCCCTCTGCATC | 57630 |
| rs190459336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235723 | TGAGACATAGTTTTG[C/T]TCTTGTTGCCCAAGC | 57630 |
| rs190460755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218657 | AACACCACCATCTCA[A/G]TCTAAAATGCAGATA | 57630 |
| rs190468966 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180325 | AGAGTCTGAGGACTC[A/G]TGTTCCAAGTCCCGC | 57630 |
| rs190488937 | snp | A/T | 0.0209421 | 0.100162 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094787 | CATTGTTTTTTTTTA[A/T]AAAAAAGGTTAATTT | 57630 |
| rs190509000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132590 | AAATGCCCTGAATAG[C/G]GACAACCTGAGTTTC | 57630 |
| rs190561735 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115110 | GTTATTCTTTCCAAT[A/G]TAACTTTCCATTTAT | 57630 |
| rs190593823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134696 | CTTCCTACTCTGATC[C/T]ATGATCCATGTCTTT | 57630 |
| rs190598250 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220071 | AAGAAATACCAAAAT[C/T]GTTTCCAATCAGTCA | 57630 |
| rs190600231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191935 | TGTGAAACTATAAAA[A/C]TTCTTGAAGATAACA | 57630 |
| rs190606842 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110850 | GAATTAATGTCAATG[A/T]CAGGCGAGACTTACA | 57630 |
| rs190608361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173443 | CTGGGATTAAAAAAA[A/T]AAAAGTAGCAAAAGA | 57630 |
| rs190616178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152706 | TGTGCCATTGCACTC[C/T]AGCCTGCGCAACAAG | 57630 |
| rs190616470 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129476 | GTTTTTAAGCAATTA[A/G]CCGTTTAGACTCTAT | 57630 |
| rs190624099 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135726 | GCCCCAGTCATCCCA[C/T]GTATTTTTATAAACC | 57630 |
| rs190627431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187243 | TCACCGTGTCACCCA[A/G]GCTAGAGCGCAGTGG | 57630 |
| rs190687054 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239548 | AAGTTAACTTCTGAA[G/T]AAATAAAAAGGCATC | 57630 |
| rs190716760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199028 | GCAGGTCTGAGTTGT[A/G]AGAAGGAAAAGGAAG | 57630 |
| rs190730642 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160609 | GAACAAACATTTGTG[C/T]ATCTGGCTGTGTTTT | 57630 |
| rs190743528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250126 | AGAATATGTTAAGCA[C/T]AGAAATTTGCAGAAA | 57630 |
| rs190743841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106108 | TGTGTATATATATTT[A/T]TTATTATTATTATTA | 57630 |
| rs190753950 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207965 | TGCACCAAAGAGAGA[A/T]GCAGGGTCCTGGGAT | 57630 |
| rs190770304 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171711 | TTTCAAGTGAAAACT[A/G]TAACAATTATGCAAG | 57630 |
| rs190840174 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130209 | GTTTAATACAACAGA[A/G]TATACTGGCTAAACC | 57630 |
| rs190911892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245808 | AGTAATTTTTAATGT[G/T]ACCAGAAACCAAAGG | 57630 |
| rs190915686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269563 | AGGCACAGAGTATTA[A/C]ATAATTCCCGCAGAA | 57630 |
| rs190922244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156323 | ATTTTTTTTTGCAAA[A/G]GGCAACACGAGCTAT | 57630 |
| rs190922612 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224554 | AACTCCTGACCTCAG[A/G]TGATCTGCCTGCCTC | 57630 |
| rs190998809 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229848 | TTAAAATCTACTTGA[A/C]ACAACACAAATATGA | 57630 |
| rs191014596 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191329 | AACCTTAGGAATATA[A/C]CTAACCAAGGAAGTG | 57630 |
| rs191029264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152242 | TCTGAAAGAATCTCC[A/G]GAGGGGAAGGGTGAA | 57630 |
| rs191058010 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231098 | AAATAGAAGGTGGTC[A/G]TAATACTTACCTCAT | 57630 |
| rs191064592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248929 | ATTAAGAAGTAGGGC[C/T]TTTAAGAGGCAATTA | 57630 |
| rs191081189 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110999 | AGAACAATTACACAA[C/G/T]TGTACTAATCAAAAA | 57630 |
| rs191082103 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229425 | TTTGTGTCCCAAATT[A/G]TGTTCCTTAGAACAC | 57630 |
| rs191086231 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207261 | AAAAGACGCCACCTC[C/T]ACAAAAAATAAAAGA | 57630 |
| rs191088316 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162077 | ACTACTTGCGAGGCT[C/G]AGGCAGTAGGCAGAG | 57630 |
| rs191092252 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190763 | AACCAGGAAAGGATA[A/T]AACCAAAAAAGAAAA | 57630 |
| rs191096508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145171 | ACAATAGCAAAGTCA[C/T]GAAATCAACCTGAGT | 57630 |
| rs191104351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171021 | ATTTTAGGCTAAAGC[C/T]ACTTCCTTATATTTA | 57630 |
| rs191155430 | snp | C/T | 1.90681e-05 | 0.00308767 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107230 | AAAAATAATGAGCCT[C/T]AGTTGGAGAATGACA | 57630 |
| rs191155962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147896 | AATCTATTCTGCTTA[C/T]TAAAGCTTTAGTTAC | 57630 |
| rs191161772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124399 | AATATAAAATCACTT[A/C]TTGTCACAAAATACA | 57630 |
| rs191167787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176510 | CAAAACCAATATTAA[C/T]ATTTACTAAGATGAA | 57630 |
| rs191197921 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255529 | GGAAGGGTGGGCAAG[G/T]TTGGGGAAGGGTAAG | 57630 |
| rs191207302 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225089 | GAGCAAAGCTCTGCA[C/T]TGATGAATTCAAAAG | 57630 |
| rs191220390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188254 | GACCAAAAGGCATGA[C/T]TGGTGAAAAACAACT | 57630 |
| rs191242269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099325 | AACTCCTTGGCTCAA[A/G]CAATCTTCCAGCCTC | 57630 |
| rs191248775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115914 | AGGACAGCAAAATGA[C/T]GAAAGAATGAGTAAC | 57630 |
| rs191308932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251701 | AAGATATCAGCAATG[C/G]AGAGTGACCTCACCT | 57630 |
| rs191369372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221015 | TGAACTCTCGTGTCG[A/C]AAGAGTTGAACACAA | 57630 |
| rs191390213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201808 | TCAAAGATTTACTAT[C/T]AAAAATCCTGGGGAT | 57630 |
| rs191396294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136753 | TATGCAGTGTCTGTT[C/T]TTCCCATGTGAGATA | 57630 |
| rs191402131 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162759 | TCCAGCTTTCTCCAG[A/G]AGTAGACTCTGCAGC | 57630 |
| rs191411513 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145684 | CGAACTCCTGACCTC[A/G]TGATCCACCTGCCTC | 57630 |
| rs191423516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246249 | ATTCCAAATTGAAGC[A/G]TGAGACACGTATTTC | 57630 |
| rs191495626 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101973 | GCATTTACAATCTTT[C/T]ATTAGTATACATTTC | 57630 |
| rs191502180 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119839 | TAATGCAGTTAGACC[A/T]GGACTGTATATTAAA | 57630 |
| rs191529750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100832 | TCCCAAACACTCCCC[A/T]AAGCCTGAACATGTC | 57630 |
| rs191534083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158601 | TCTGGCAGTAGTGTG[C/G]AAAATGGACGTGAAG | 57630 |
| rs191539920 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140841 | ACAGGATACAAACAG[C/T]AGATCTGAGAAGTAA | 57630 |
| rs191554240 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244870 | AGTGGTATATAAGAC[C/T]GTGTGAAAAAAGGTA | 57630 |
| rs191559863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178000 | TGGCTCATGCCTTTG[G/T]AAGTCTGAGGTGAGT | 57630 |
| rs191561987 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203267 | AAAAATATCCCAGAA[C/G]TGGCCAAGCACGGTG | 57630 |
| rs191564086 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101563 | CAACATGAATGTACT[C/G]AATGCCACTGAATTG | 57630 |
| rs191574785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139816 | TACCTAACTTTGGGG[C/T]CTTAAGGGAGCCATC | 57630 |
| rs191631088 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123350 | CTGAGTGGAAAAAAA[A/T]TTCAAATTTCTAGAC | 57630 |
| rs191638462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253521 | ACTAATTTATTCTAA[C/T]TGCCCTTTTCTTCCC | 57630 |
| rs191644565 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233094 | TCTCTACTAAAAATA[C/T]AAAAATCAGCCAGGC | 57630 |
| rs191656225 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213546 | GAATTTCAGCTTATC[A/G]AATGTTTCTTTCATA | 57630 |
| rs191661120 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266008 | ATCAGCAGTGTCCCT[C/T]TCCCTATGGCTCATT | 57630 |
| rs191704466 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200430 | TAAAATCTCCACAGT[C/T]AGAAAATTTTAAAGC | 57630 |
| rs191721930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161793 | ACTTTCAGAAACTTT[C/T]CAGAAAGAACTGAGG | 57630 |
| rs191787679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217339 | CTGGGAAGAAATCTA[C/G]AAGCCAACGAGCAGA | 57630 |
| rs191787870 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198222 | AATTGGTTTTCAGGT[G/T]ACTGTGGCTTTCAAC | 57630 |
| rs191794723 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179731 | CAATTTCACTGTTTA[C/T]TTTAGCTCATTCTTT | 57630 |
| rs191795271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268354 | CTGTGTATTCATAAA[A/T]CCAATAGAATGATTC | 57630 |
| rs191803913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159756 | AATGCATTTGTCTCT[C/T]CACAGCTGGATGCTT | 57630 |
| rs191812097 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094422 | AAAACCAATAGAAAA[C/T]CCATACATTATATTA | 57630 |
| rs191812542 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196505 | AAGTAATTTGAGAAC[C/T]AGGATATTATTAACA | 57630 |
| rs191812982 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141843 | TTTGAGATGGAGTCT[C/T]GCTCTGTTGCCCAGG | 57630 |
| rs191820326 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111671 | TAGTTGATCAAATAA[C/T]GAAGACTTTGAACTG | 57630 |
| rs191821839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224140 | CACTAATTTCTAAAC[A/G]CTCCTATGAGGGACA | 57630 |
| rs191824440 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158011 | CCCAAAGTGCTGGGA[A/T]TATAGGCATGAGCCA | 57630 |
| rs191847811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119552 | ATTTCTCTTATCCAT[C/T]ATTATCATTATTTTG | 57630 |
| rs191877950 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094490 | TTATACCAGGAAACT[A/C]TGAACAGAGGTACTT | 57630 |
| rs191893029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111911 | GACAAAAATGCAATG[C/T]CTAGAGATCCCTGAG | 57630 |
| rs191900918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131647 | GAAAACCTTAACTTT[A/C]CACGCCTAAGTAACA | 57630 |
| rs191913630 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106601 | GGACACAATTCAGGC[A/G]TGGCAGAGTAGAGAA | 57630 |
| rs191928966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258936 | TCACATTTCCAGGAA[C/T]TTTATACAAATGCTA | 57630 |
| rs191951562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237874 | CAATTTATGATTTCC[A/C]CCCCGCTCCACACCC | 57630 |
| rs191969119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263007 | AACAAACAAACAAAA[C/T]CCACCTTTTCCGTTT | 57630 |
| rs191992846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220452 | CTCTCCTCCACAGGA[C/T]AAATTTTCCTTTTTC | 57630 |
| rs192003422 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181541 | GCTAGGATTACAGGC[A/G]TGAGCCACCGCGCCA | 57630 |
| rs192010078 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181040 | TAGTAAAATAGATGA[A/T]ATCTGAAATGTAGCC | 57630 |
| rs192025309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144402 | GGCAAAGACTTCTGT[G/T]TTGGGAATAGGGTCC | 57630 |
| rs192027857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151925 | TCATTCATATTTTTT[G/T]CTTGCTTAAGAATCA | 57630 |
| rs192040124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205365 | CTTGTCAGATTTCTA[C/T]CATAAAAACTAATTT | 57630 |
| rs192042735 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189467 | CCAGAACAAGATCCA[C/T]GCCAGGGCAGGAAAG | 57630 |
| rs192047134 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114317 | CTGCTTCACCATCAC[A/G]TCTCCTTCTCTGGCC | 57630 |
| rs192060577 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168721 | AAATGAACAGTCTCA[C/T]GTTTGGTTCTGCCCA | 57630 |
| rs192060964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239372 | AGCCAAGCATACAGA[A/G]AAATAATGAGAGGTT | 57630 |
| rs192066671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149416 | TGTATCAAGTGGATA[C/G]CATTCAGAAGATATG | 57630 |
| rs192073068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259241 | GCTAACAGAAAAATG[C/T]TCAACATTGACAGCC | 57630 |
| rs192149589 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097984 | CAGAAAAAGTGATGT[G/T]AATAAGCCATCTTAG | 57630 |
| rs192181228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096743 | GTGATTTTAAAAAAT[A/G]GTGTACTGTTAGTCT | 57630 |
| rs192240872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252731 | GACAGAGAATAAATA[C/T]GTGCTGATGGACTGA | 57630 |
| rs192254144 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211628 | CTGTACTTAGTACAA[C/T]TCAAATGAAGGCCTG | 57630 |
| rs192270156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175350 | TCCTGTGGCTCCCAA[A/G]GCTTTCTATCATCTG | 57630 |
| rs192309154 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241155 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGATTGC | 57630 |
| rs192316928 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108117 | GAATGTTCTTTCTGA[C/T]GACCAAGCTTAACAT | 57630 |
| rs192325390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201073 | AATACAGTATTGTCA[C/T]CATTTCTGATTACTG | 57630 |
| rs192342485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247225 | CAAAAGGGAAGAGGT[A/G]GGGAAAAGAGCAAAA | 57630 |
| rs192346554 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272628 | ACTGGGCAGATAGAT[A/G]AAGATGAGGCTGACC | 57630 |
| rs192347773 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226264 | AAGAGTATATTTTGT[C/T]TCTGAAATTAATTTA | 57630 |
| rs192363981 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205678 | GAGCCCAATGAATGA[C/T]GTTAGCAGGACTAAT | 57630 |
| rs192368995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190107 | TTCATAGCCCTAAAC[A/G]CCTACATCAAAAAGT | 57630 |
| rs192385451 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134137 | GCACTTCAAACACCT[C/T]CCAGCCTCTTCTAGA | 57630 |
| rs192401543 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095304 | AGGGAGCGAGTGCAC[C/T]GAAGAGACCTTGGTC | 57630 |
| rs192420361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132889 | CACTCATGTCACAGT[C/G]ACAGACACTCATGAA | 57630 |
| rs192495173 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185268 | CCACACCTGAATGCA[A/G]GGAGAACAGCCAAGA | 57630 |
| rs192503039 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231824 | CATCAAATACCTACT[A/T]CATGTCAGGTACTGT | 57630 |
| rs192508455 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163948 | AGATCAATGATCTGA[C/T]TCTTGTGTGGGTCAA | 57630 |
| rs192515043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210095 | GGCACCATGCCTGGA[C/T]TCTACACGCCATTTT | 57630 |
| rs192521319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192249 | CATGAATAGACAGTT[A/C]GCAAAAGAAGATATA | 57630 |
| rs192523056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125357 | CTAGTGACACTGTGA[C/G]TGAAAAGTTCAAGTA | 57630 |
| rs192575208 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242122 | TTTTCTATTTCAATT[A/T]AAATTTTTTTTTTTG | 57630 |
| rs192599287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201855 | AAACCCATCTGTCGT[C/T]GCTACAGAGGCAAGT | 57630 |
| rs192620376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163578 | ATAATTCCTGAAACA[C/T]GGTTTTGTCCACATC | 57630 |
| rs192650152 | snp | C/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232795 | ACCCCTCTTCAGTGA[C/T]ACACTTCAAAGCCAG | 57630 |
| rs192657030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109545 | CAGAAAAGATGCTGT[C/T]CTAGTTCCAAGGAAC | 57630 |
| rs192666514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192451 | ATACCACCTTATTCC[C/T]GCAAGAATGGCCACA | 57630 |
| rs192669374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127218 | TACATGTGAAATGTA[C/T]GGGACAATGTTTATA | 57630 |
| rs192683630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154398 | ACAATGATACAGTTT[C/G]TCATTTTAGTTTTCA | 57630 |
| rs192691295 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252064 | GTTCCGCAGCGACTC[A/G]AGAACCACGTGAGAT | 57630 |
| rs192732292 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148559 | ACATGATTATATTGT[A/G]GAAATAAAATCATTA | 57630 |
| rs192761255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112580 | TTGCAAATCATCCCT[A/G]CAGATGAAAACATAG | 57630 |
| rs192781952 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121252 | CAAATAGTATTTGCA[C/T]AGTGTGAAAGAATTA | 57630 |
| rs192851407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222320 | AATACAAAAAATTAG[C/G]CAGGCATGGTAGCAG | 57630 |
| rs192855622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184737 | TATTTATTTATTTTT[G/T]GCACACTGGCTAAGA | 57630 |
| rs192861211 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217961 | TCCTATGGTTTTCCA[A/T]ATCATCACAACACAA | 57630 |
| rs192870363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246556 | TGAGGGTGTGACTGT[C/T]TATTTAAGCATGCAA | 57630 |
| rs192874566 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180122 | AGCCAGACCATCTGC[A/G]TGACAGCAAAGGCTA | 57630 |
| rs192933432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167907 | ACTGGAAGGCCAAGG[C/T]GGTAGGATATCTTGA | 57630 |
| rs192946987 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126358 | TCTGACCATATCCTA[C/G]TCTTCACCCTGATTT | 57630 |
| rs192982259 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130643 | TGACTTCTACCTTTC[A/G]GTGGGGATGCATAAT | 57630 |
| rs192984366 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103713 | GTGAGACAGATCTAA[C/G]AATCCAAGGTAAATA | 57630 |
| rs193035579 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236445 | AAGCCTTTGCTGTAT[G/T]AAGCATCTCAAATTT | 57630 |
| rs193043646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169006 | CATGACCTTCTACAA[C/T]GTCATTAGGAAAAGC | 57630 |
| rs193047647 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197215 | CCATGTTGGCTAGTC[C/T]GCTCTTGAGCTCCTG | 57630 |
| rs193067469 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271377 | AATGGAGCCACCGGA[C/T]GGGAAGGCGGCGGGA | 57630 |
| rs193072249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198640 | GTATAAATCTTTACA[C/T]ATGTATACATAAGTA | 57630 |
| rs193074479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225603 | AGACTGTCAAGACTG[C/T]AGTTTCATCAAGACA | 57630 |
| rs193083798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160375 | AAAACAAATCTATTA[C/T]ATGTTCCTAAAATCA | 57630 |
| rs193107855 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153171 | TTCTTTTATTTGATT[A/T]TTACCATGCTCTGGT | 57630 |
| rs193136333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115511 | CTAATGCCTGAGGAT[A/C]TGTCACTGTCTGCCA | 57630 |
| rs193143204 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266306 | AACATTCCACGTTAT[A/C]ACTTTCAGCTTTGCA | 57630 |
| rs193151277 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222886 | CTAAAATGGCAAGTT[C/G]TCAGCTGTCTATGAA | 57630 |
| rs193174775 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108687 | TCCTCAGCTGATCTT[A/C]TGCGCTTTCGCTTCA | 57630 |
| rs193180592 | snp | A/G | 0.292523 | 0.246357 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145867 | TTCTATATAAAATAT[A/G]TATTCTATATATTAT | 57630 |
| rs193221732 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257829 | AGAGCTTAATCCAAA[G/T]TCAGGCTCCCTAAAC | 57630 |
| rs193222824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216643 | CCCAGTGGTTTGAGA[C/T]CAGCCTAGGTGATGA | 57630 |
| rs193226644 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150622 | ATATCCTTTGACCTA[C/T]GCTACCCCCAGGGGG | 57630 |
| rs193227660 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179234 | AACTTTGCTGGCTTT[A/G]AAGACAAAAGGAGAG | 57630 |
| rs193260678 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174866 | TGTGGATCTACACAA[A/C/T]GATGTCTCCCAGATC | 57630 |
| rs193265350 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135951 | CGAGTTTGGACCATG[A/G]CATCTTAAATCTGGG | 57630 |
| rs193287298 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098743 | ACACTGGCCTAAGGA[C/T]TGACACAGTCTTTAA | 57630 |
| rs193299025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242403 | TGGAAAAAGAGATTT[A/G]AAATATTAAATTCAT | 57630 |
| rs193301776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202227 | CGGGAAGACAAGGAA[C/T]AGTGTTAGTGCTTTG | 57630 |
| rs199505862 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114333 | CTCCTTCTCTGGCCC[-/T]TAAGCTTCCTGCCTC | 57630 |
| rs199529724 | snp | A/C/G | 1.68255e-05 | 0.00290043 | missense, synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107011 | AGTCGTGACCGGTCC[A/C/G]TCCCCGTCCACAGGG | 57630 |
| rs199530964 | in-del | -/C | 0.120326 | 0.21374 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249050 | GCTAACTCGGTGAAA[-/C]CCCCATCTCTACTAA | 57630 |
| rs199540496 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178317 | TTAAAAAAATAAGCA[A/T]CTATGCTTATTTAAA | 57630 |
| rs199546269 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177074 | CAGATGTAAGCCACC[-/T]CCCCCAGCCTACAAC | 57630 |
| rs199598827 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099843 | GTTTTATAAACCTCT[-/G]GGGGGGGCGGGTGGA | 57630 |
| rs199602308 | snp | A/G | 0.000492841 | 0.0156901 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130016 | CTAAAGACCTAAAAG[A/G]GAAATAAAAATGGGA | 57630 |
| rs199611066 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140709 | AATATAGCCTTTTTT[-/A]AAAGGCGGGACTTAC | 57630 |
| rs199625815 | snp | A/G | 0.000184857 | 0.00961219 | missense | SH3RF1 | GRCh38.p7 | 4:169107000 | CCTGCCACTGCAGTC[A/G]TGACCGGTCCGTCCC | 57630 |
| rs199707688 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187897 | ATCCGCAAAGTTAAA[A/C]TGAGGTCATGCTGGA | 57630 |
| rs199744067 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253841 | ATTTTCCTCTATGTC[A/G]GAATGATGTGCCTGG | 57630 |
| rs199745243 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242122 | CTATTTCAATTTAAA[-/A]TTTTTTTTTTTGTAG | 57630 |
| rs199752164 | in-del | -/AG | 0.0337553 | 0.125452 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125469 | TTAGGATCTGGCTAA[-/AG]AGAGGGGAAGTAGTC | 57630 |
| rs199769054 | in-del | -/AAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230856 | GTGAGAAACCACCTC[-/AAAA]AAAAAAAAAAAAAAA | 57630 |
| rs199772454 | in-del | -/A/AA | 0.486 | 0.0824865 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183750 | TTAAAAAAAAAAAAA[-/A/AA]CAAAACAAAACAGAA | 57630 |
| rs199773241 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197539 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 57630 |
| rs199775839 | in-del | -/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273060 | CTTTTCTTTTCTTTT[-/C]TTTTTTTTTTTTTGA | 57630 |
| rs199784272 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178331 | AACTATGCTTATTTA[A/T]AAAAATAAGCAACTA | 57630 |
| rs199805065 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212453 | TACAAGAGAATGACA[A/C]AATAATCCCAGGACT | 57630 |
| rs199806800 | snp | C/T | 0.000127701 | 0.00798963 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116602 | GGGTGTCACTGCTGC[C/T]GTGGGGCGTTCCTGG | 57630 |
| rs199812652 | in-del | -/AT | 0.0839998 | 0.186933 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218447 | TATAGAATATAATAC[-/AT]GTTATATAATATATA | 57630 |
| rs199824103 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206968 | TTCTCTTTTTTTTTT[-/T]GAGACAGGGTTTCAC | 57630 |
| rs199855205 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248336 | AGTTCATGTCCTTTG[C/T]AGGGACATGGATGAA | 57630 |
| rs199862553 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227611 | CTGGGATCCCTGGGG[-/T]GTTCCATAACATCTA | 57630 |
| rs199890582 | snp | A/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094745 | AAGTATTTTTTTTTT[A/T]AATTCAACACACAGG | 57630 |
| rs199893755 | in-del | -/G | 0.0205511 | 0.0992634 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271229 | ACCCCGCCGGAGCCC[-/G]GGGGGCGGGATTGGG | 57630 |
| rs199942841 | snp | C/T | 0.000399281 | 0.0141238 | missense | SH3RF1 | GRCh38.p7 | 4:169117718 | GACTGACCATGGTCA[C/T]TCCCCGACTTGTCTG | 57630 |
| rs199943944 | in-del | -/AA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117424 | ATGTTGTTCATTATT[-/AA]AATTACATCTACATT | 57630 |
| rs200026352 | snp | C/G/T | 6.83695e-05 | 0.00584643 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169130088 | TGATGGGAAAGTAAA[C/G/T]GAGGGGCCAGTTGTC | 57630 |
| rs200064173 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102915 | TGCCCCAGTCACATT[C/T]TTTTTTTTTTTTTTT | 57630 |
| rs200075914 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221850 | GTAAAGATCCAAAAT[C/T]GTTACACAGTACAAA | 57630 |
| rs200092278 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192921 | TATCATATATATGTG[A/T]TATATATATATATGA | 57630 |
| rs200092973 | in-del | -/ATATGTGATATATATATCATATAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192813 | ATATATATATGATAT[-/ATATGTGATATATATATCATATAG]ATGTGATATATATAT | 57630 |
| rs200104392 | snp | C/T | 0.000700966 | 0.0187081 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106984 | CTGGGCCAGGGCTGC[C/T]CCTGCCACTGCAGTC | 57630 |
| rs200110734 | snp | A/G | 3.29712e-05 | 0.00406011 | missense | SH3RF1 | GRCh38.p7 | 4:169122110 | CTTACACACTGGGGC[A/G]AGTCTGCGGCCGTAA | 57630 |
| rs200119474 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238974 | TTTCCGCCCCCCCCC[-/A]CCCCTTGCCCTTTTT | 57630 |
| rs200143189 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180258 | AAAGAGGTATAGAAA[A/G]GAAAAGAAGAGTTAA | 57630 |
| rs200193001 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180259 | AAGAGGTATAGAAAA[A/G]AAAAGAAGAGTTAAA | 57630 |
| rs200213891 | snp | C/G | 3.32751e-05 | 0.00407878 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121028 | TTTCAGGTTGAGTAA[C/G]AGACAAATCCCAAGA | 57630 |
| rs200242801 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175713 | CCAAAACCACTAGAC[A/C]ATAAGCTCTAAAAAA | 57630 |
| rs200269942 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238974 | TTTCCGCCCCCCCCC[A/C]CCCCTTGCCCTTTTT | 57630 |
| rs200277355 | in-del | -/AT | 0.02016 | 0.0983543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192783 | TTCATATATATATAC[-/AT]ATATGTTTCTTTTAT | 57630 |
| rs200308175 | in-del | -/ATAGA | 0.122758 | 0.215196 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218312 | ATATAAATATAGAAT[-/ATAGA]ATATAGAATACAGAT | 57630 |
| rs200334711 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244426 | GTATTTTTTTTTTAA[A/G]CCACTGCACAGATGA | 57630 |
| rs200350968 | in-del | -/AAC | 0.0345262 | 0.126772 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163253 | AAAAAAAAAAAAATG[-/AAC]AACAGTTTTCCAAAT | 57630 |
| rs200361446 | in-del | -/TT | 0.0737376 | 0.17729 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111432 | GCTAATTAAAAATAA[-/TT]TTTTTTTTTTTGGTA | 57630 |
| rs200390218 | in-del | -/T | 0.26737 | 0.249396 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224322 | TGATCTAATTTCCTA[-/T]TTTTTTTTTTTTTGA | 57630 |
| rs200436648 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169603 | ACTGTTTCAAAAAAT[-/A]AAAAAAAAATAAAAA | 57630 |
| rs200485669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211253 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCATGAGT | 57630 |
| rs200503325 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135174 | ACCCCATCTCTATTA[A/C]AAACAAACAAACAAA | 57630 |
| rs200517842 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178318 | TAAAAAAATAAGCAA[C/T]TATGCTTATTTAAAA | 57630 |
| rs200527865 | snp | C/G/T | 3.5392e-05 | 0.00420651 | synonymous-codon, missense | SH3RF1 | GRCh38.p7 | 4:169106876 | AGGTCTAGACTCATT[C/G/T]AAGACAGGACCCAGG | 57630 |
| rs200554066 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247881 | TATGCAGCCAACAAA[C/T]ATGAAAAAAAGCACA | 57630 |
| rs200557362 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144935 | GGTAAGAGGAAAAGC[-/A]AAAGGCCCTCAGAAT | 57630 |
| rs200582903 | snp | A/T | 0.000153988 | 0.00877327 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106918 | CTGGCGAGGAGGTGG[A/T]GCGATGGGAACTGCG | 57630 |
| rs200590969 | in-del | -/TGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146104 | ATATTCTATATAAAA[-/TGT]TATATATTCTATATA | 57630 |
| rs200598397 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243236 | TGAAAAGCTCACTTG[C/T]TCTAAGGTATAATTT | 57630 |
| rs200626141 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165398 | TAAAGAGGTTGGGTA[A/C]CAGCCACATGCAGTG | 57630 |
| rs200626375 | snp | C/T | 0.00054338 | 0.0164741 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136303 | TTTTTATATAACACT[C/T]GTTTGAGGATTTACC | 57630 |
| rs200649803 | snp | A/C/G | 0.000131772 | 0.00811605 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107215 | TTCTTTCTGGAAAAA[A/C/G]AAAATAATGAGCCTT | 57630 |
| rs200656517 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154926 | CTCTAAAAAGACTTT[A/C]CTATGTCAAGCTTGG | 57630 |
| rs200702719 | snp | A/G | 3.31791e-05 | 0.00407289 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116464 | ACTGGCTCGACTGAT[A/G]CTGATGGCAGCAGTG | 57630 |
| rs200707312 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136743 | AAAGTTTGCCTATGC[A/G]GTGTCTGTTTTTCCC | 57630 |
| rs200749874 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178332 | ACTATGCTTATTTAA[A/T]AAAATAAGCAACTAT | 57630 |
| rs200785590 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192781 | TTTCATATATATATA[-/TA]CATATATGTTTCTTT | 57630 |
| rs200790356 | snp | C/G | 1.83876e-05 | 0.00303207 | missense | SH3RF1 | GRCh38.p7 | 4:169268821 | TGTAGGCTACTTACC[C/G]TCACTGGGGGGCTCC | 57630 |
| rs200823549 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168215 | AGAATGGCAAAATGA[A/G]AAAAGAAATCTGAAA | 57630 |
| rs200854924 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126600 | TTATTTTTATTTTTG[-/T]TTTTTTTTAGGAACA | 57630 |
| rs200886298 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133462 | CTGGGAGACAACAGC[-/A]AAAACTCCATCTCAA | 57630 |
| rs200913181 | in-del | -/C | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191314 | AAAAAAAAAAAAAAA[-/C]ACCTTAGGAATATAC | 57630 |
| rs200935929 | snp | C/T | 7.07626e-05 | 0.0059478 | missense | SH3RF1 | GRCh38.p7 | 4:169122188 | CAGCAGCAGCAGCAG[C/T]GGCGGTGGCGCCTGG | 57630 |
| rs201034830 | in-del | -/TAT | 0.119978 | 0.213528 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145771 | ATAAAATATATAAAA[-/TAT]TATATATTCTATATA | 57630 |
| rs201050669 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198356 | AACAGTCTACAAATA[G/T]AGTGTTAAATCAGCA | 57630 |
| rs201059210 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178281 | AAAAAAATTTTTTTT[A/T]AAATAAGCAACTATG | 57630 |
| rs201060822 | snp | C/T | 0.000399281 | 0.0141238 | missense | SH3RF1 | GRCh38.p7 | 4:169122155 | CAGTGGATCCTGCCA[C/T]GGGCCTCGGTCCCAT | 57630 |
| rs201073877 | snp | A/T | 1.65825e-05 | 0.00287941 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121012 | AGAAAATAATATTTG[A/T]TTTCAGGTTGAGTAA | 57630 |
| rs201107227 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192922 | ATCATATATATGTGA[G/T]ATATATATATATGAT | 57630 |
| rs201151193 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182856 | CAACCAAAAAAAAAA[-/A]GGAGAAAGGTGGTTT | 57630 |
| rs201155341 | snp | C/T | 1.77426e-05 | 0.00297842 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156715 | TGAATTTTAATAAAA[C/T]AATGGTCTTAAAATG | 57630 |
| rs201156238 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178330 | CAACTATGCTTATTT[A/T]AAAAAATAAGCAACT | 57630 |
| rs201161581 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247884 | GCAGCCAACAAACAT[A/G]AAAAAAAGCACATCA | 57630 |
| rs201164850 | snp | C/G | 1.64814e-05 | 0.00287061 | missense | SH3RF1 | GRCh38.p7 | 4:169117547 | CAGCATTGCGGGCCT[C/G]GTTGACTGTCATTTG | 57630 |
| rs201263380 | in-del | -/G | 0.0520825 | 0.152737 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180064 | ATGGGGACGTAAGCA[-/G]AAACAAAAGAAAAAA | 57630 |
| rs201323343 | snp | A/G | 3.35542e-05 | 0.00409585 | missense | SH3RF1 | GRCh38.p7 | 4:169136547 | TGGGCTGCTGCCGAG[A/G]AACATTCTCCAGCAT | 57630 |
| rs201361776 | in-del | -/GT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219978 | TCAGTACAAACTAGC[-/GT]GTGGTACTCTAAATT | 57630 |
| rs201412933 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102395 | AAAGATCATACATAG[-/A]TTTTTTTTTTTCCCC | 57630 |
| rs201420903 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244427 | TATTTTTTTTTTAAG[C/G]CACTGCACAGATGAT | 57630 |
| rs201435493 | in-del | -/TGTGTGTGTGTGTGTGTGTGTGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187517 | TTTACAACGAATTTC[-/TGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57630 |
| rs201441442 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224336 | ATTTTTTTTTTTTTT[G/T]AAATGGAGTCTTGCT | 57630 |
| rs201445783 | snp | A/C/G | 4.96874e-05 | 0.0049841 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096701 | GCCTAGAAAAGAAAG[A/C/G]GATTTTGGTTAAGGC | 57630 |
| rs201500426 | in-del | -/AGAATAC | 0.499515 | 0.0155675 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218321 | TAGAATATAGAATAT[-/AGAATAC]AGATTATAGAATATA | 57630 |
| rs201575808 | snp | C/T | 0.00199792 | 0.0315431 | missense | SH3RF1 | GRCh38.p7 | 4:169120844 | GTGCCACATAATTGC[C/T]AGGGAAAACCCCTAT | 57630 |
| rs201599307 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168217 | AATGGCAAAATGAGA[G/T]AAGAAATCTGAAATT | 57630 |
| rs201613193 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183759 | CTCTTTAAAAAAAAA[-/C]AAAACAAAACAAAAC | 57630 |
| rs201613449 | in-del | -/AAT | 0.0170251 | 0.090679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147953 | ATAATAAAATATTTA[-/AAT]AATAAAAATAAAAAG | 57630 |
| rs201628132 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125201 | ATGGCCTTTGGGGTC[-/A]AAAAAAAAACATAGA | 57630 |
| rs201631978 | in-del | -/AG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218307 | ATATAATATAAATAT[-/AG]AATATAGAATATAGA | 57630 |
| rs201686417 | in-del | -/TG | 0.0126979 | 0.078662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254934 | AGAGGAGGTCAGGGC[-/TG]CACCACAGCCTGCAA | 57630 |
| rs201695335 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178333 | CTATGCTTATTTAAA[A/T]AAATAAGCAACTATG | 57630 |
| rs201698754 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192918 | ATATATCATATATAT[A/G]TGATATATATATATA | 57630 |
| rs201705013 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227607 | GTAGCTGGGATCCCT[G/T]GGGTGTTCCATAACA | 57630 |
| rs201743684 | snp | A/C/T | 6.78592e-05 | 0.00582457 | missense | SH3RF1 | GRCh38.p7 | 4:169269160 | GCAGAAGCATCAAGG[A/C/T]GCTCTAGACACACCG | 57630 |
| rs201747227 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166112 | GAAATTGAAAAATTA[-/G]GTTCAACAACAAAAG | 57630 |
| rs201759331 | in-del | -/ACACACACACACAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255623 | CATACATACACACAT[-/ACACACACACACAC]ACACACACACACACA | 57630 |
| rs201764689 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110097 | TGAACGTTAGAGGCC[A/G]GGCACAGTGGCTTAC | 57630 |
| rs201767383 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192809 | TTTTATATATATATG[-/AT]ATATATGTGATATAT | 57630 |
| rs201773486 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226490 | GGAGCCTGATTTAAA[A/G]AAAAAAAAAAAAGAG | 57630 |
| rs201789165 | in-del | -/TC | 0.0232847 | 0.105357 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273059 | TCTTTTCTTTTCTTT[-/TC]TTTTTTTTTTTTTTG | 57630 |
| rs201789263 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268753 | GAAAACACCAAGCTA[-/T]AAGAATAAAGAAAAA | 57630 |
| rs201812152 | in-del | -/T | 0.0614824 | 0.164198 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231576 | GTCTCAAAAAAAAAA[-/T]TTTTTTTTTTAATAA | 57630 |
| rs201813018 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269371 | TAGGGAAAAAGTTCA[A/C]AGGAGCCAAGAATCA | 57630 |
| rs201873199 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224434 | GTGATTCTCCTGCCT[C/T]AGCCTCCCAAGTAGC | 57630 |
| rs201882003 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156684 | TGAGGTATACCCTTT[A/T]AAAAAAAAAGAGGGA | 57630 |
| rs201900968 | snp | A/G | 0.00747115 | 0.060661 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136423 | GATCTCCATGGAGTG[A/G]CGGTTCTGGGATGCC | 57630 |
| rs201941357 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238973 | ATTTCCGCCCCCCCC[A/C]ACCCCTTGCCCTTTT | 57630 |
| rs201951489 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241579 | ACTCCTGAACTCCAC[A/C]AGAGGAGACAGTGAG | 57630 |
| rs201979539 | in-del | -/A | 0.355311 | 0.226737 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106492 | AAAAGGCAAAAAATT[-/A]AAAAAAAAAAAGACA | 57630 |
| rs202007715 | in-del | -/AT | 0.0236746 | 0.106192 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192281 | AAATGGCCAACAAAC[-/AT]ATGAAAAAAATGCTG | 57630 |
| rs202026335 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218308 | TATAATATAAATATA[-/G]AATATAGAATATAGA | 57630 |
| rs202026605 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110026 | CAAAAAAAAAAAAAA[-/A]CCACCTGGGAGGAGG | 57630 |
| rs202060267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174187 | CTCTCTTCAGCCCCT[C/T]GAAAGCTGTGACTAC | 57630 |
| rs202088424 | in-del | -/AAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168215 | GAATGGCAAAATGAG[-/AAA]AAAAGAAATCTGAAA | 57630 |
| rs202092850 | in-del | -/A | 0.0115144 | 0.0749975 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095969 | CCAAAGAAGAAAACC[-/A]AATTAGAGAACTGGG | 57630 |
| rs202095407 | in-del | -/CTCCACAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241572 | ATCAGCACTCCTGAA[-/CTCCACAG]CTCCACCAGAGGAGA | 57630 |
| rs202117650 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231576 | GTCTCAAAAAAAAAA[A/T]TTTTTTTTTTAATAA | 57630 |
| rs202139578 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148028 | TTTTTCTCATAAAAA[C/T]GCAACCTCAGATATT | 57630 |
| rs202145964 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244424 | CAGTATTTTTTTTTT[A/T]AGCCACTGCACAGAT | 57630 |
| rs202156267 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107814 | CTTGATTAAATGTAA[G/T]AAGCCAATAAAACAG | 57630 |
| rs202197285 | in-del | -/AAC | 0.0225045 | 0.103662 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228952 | TTCTGTTCTTCGAAA[-/AAC]AAACAAACAAACAAA | 57630 |
| rs202225553 | in-del | -/ATGTTAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146103 | TATATTCTATATAAA[-/ATGTTAT]ATATTCTATATATTC | 57630 |
| rs202233981 | snp | A/G | 0.000132107 | 0.00812626 | missense | SH3RF1 | GRCh38.p7 | 4:169136508 | TTCTTCTTGGTGTCG[A/G]AGTGCTTTGGGGCAG | 57630 |
| rs202243296 | snp | C/G | 1.74891e-05 | 0.00295707 | missense | SH3RF1 | GRCh38.p7 | 4:169136405 | GATGAGGACAGGGGG[C/G]CTGATCTCCATGGAG | 57630 |
| rs207465247 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197035 | TTTTGAGACATTGTC[A/T]CACTCTTTCATCCAG | 57630 |
| rs367550186 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144472 | TTTACTCACCCAAAT[A/G]TTTTTTGAGTGACTG | 57630 |
| rs367560767 | snp | A/G | 3.31126e-05 | 0.00406881 | missense | SH3RF1 | GRCh38.p7 | 4:169116367 | GAACGGTCACTATCC[A/G]GCCACTGGGCTCAGC | 57630 |
| rs367572213 | snp | C/G | 1.69404e-05 | 0.00291031 | missense | SH3RF1 | GRCh38.p7 | 4:169136556 | GCCGAGGAACATTCT[C/G]CAGCATCAACTCCTG | 57630 |
| rs367663077 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260824 | GGAAACCAACATAAC[G/T]GAGTTCATGTCTGTA | 57630 |
| rs367675572 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111353 | TTGACCTCCTGGGCT[C/G]AAGCCATCCTCCCAC | 57630 |
| rs367692797 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203331 | TGAGATTGGTGGATC[A/G]CTTGAATCCAGGAGT | 57630 |
| rs367726071 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177856 | ATGTGTATGTATATA[-/AT]ATATATATATATGCT | 57630 |
| rs367784593 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198983 | ACTGGAGCTTCTAAA[A/G]GAATACTTTAAGGAC | 57630 |
| rs367787830 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156700 | AAAAAAAAAGAGGGA[A/T]GAATTTTAATAAAAT | 57630 |
| rs367788722 | snp | A/G | 0.021333 | 0.101051 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221527 | CAACAACTCAGTTCC[A/G]AGAAAAGTTTGAAAA | 57630 |
| rs367823076 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131626 | TTCCCAGAACTAAAC[C/T]GAAAAGAAAACCTTA | 57630 |
| rs367827657 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109617 | GAAGAATGTTCCACT[C/T]GAGAGAGATCATTTT | 57630 |
| rs367840075 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141628 | ATTTTTCTTATAGAC[C/T]GATATAAATACTTTT | 57630 |
| rs367840557 | snp | C/T | 3.32408e-05 | 0.00407668 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120813 | ACAATGTATTCAAAA[C/T]CATACCTTGTGACTG | 57630 |
| rs367896305 | snp | C/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272593 | CAAACTGAAAGTTAC[C/T]ACTTAGTTCTGCATG | 57630 |
| rs367905852 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259444 | TCTTTAAAATGGCTG[C/T]GTTTACAGCCACCCA | 57630 |
| rs367912149 | snp | A/G | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094137 | CTGTAGACATCTTCC[A/G]CTTGAGATGTATGCA | 57630 |
| rs367966174 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248487 | CACCAGGGCCTGTTG[C/T]GGGGTGGGAGGCAAG | 57630 |
| rs368021658 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221793 | ATCACTTACGTAATA[C/T]CTGAATTCTACAACT | 57630 |
| rs368033119 | snp | A/G | 3.31033e-05 | 0.00406823 | missense | SH3RF1 | GRCh38.p7 | 4:169155484 | GATTAATTTACCTCA[A/G]CATATGAAATTGGAA | 57630 |
| rs368033713 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267585 | TTAAATAAATAAATA[A/C/T]GTCAAAAGAAACCTG | 57630 |
| rs368065147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111073 | AGCACTTTGGGAGGC[C/T]GAGGCAGGGGGATCA | 57630 |
| rs368116510 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123674 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 57630 |
| rs368156996 | snp | A/G | 0.000698405 | 0.0186739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121030 | TCAGGTTGAGTAACA[A/G]ACAAATCCCAAGATG | 57630 |
| rs368167796 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175897 | GGGACCTTTGGAAGG[C/T]AATTAGGTTTGGTTA | 57630 |
| rs368212224 | snp | A/G | | | missense | SH3RF1 | GRCh38.p7 | 4:169122164 | CTGCCATGGGCCTCG[A/G]TCCCATTCCAGCAGC | 57630 |
| rs368256701 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253076 | GGAAAAGTTTGGATC[A/G]CAAAGAAGAAACTTA | 57630 |
| rs368278880 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176869 | CTTGATTAAAACCAC[C/T]TGTGCTGGGCATGGT | 57630 |
| rs368314494 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100755 | CCTGGTATGCGAAGC[C/G]CTTGGTGATCAGGCC | 57630 |
| rs368342415 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234496 | ATTTTGGTGAAGTTC[A/G]TTTGGGTGAAGAACA | 57630 |
| rs368347109 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184027 | CTAAATCTGTTACCT[A/G]GGATGTAGCAGTAAG | 57630 |
| rs368362893 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127498 | TTTTCCACTTAAACC[C/T]GACATATTAAATCTA | 57630 |
| rs368377526 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222073 | TACATTCAAACCACC[-/T]TTTTGGGTTTTCTTA | 57630 |
| rs368384789 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162919 | TGCTGCCCTGCTCAC[A/G]CTCATCTGTGGGCTC | 57630 |
| rs368469653 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198125 | GCAATATTTGTGAGT[C/T]GGAGAAAAAGGCAAA | 57630 |
| rs368474589 | snp | A/C | 1.68417e-05 | 0.00290182 | missense | SH3RF1 | GRCh38.p7 | 4:169107038 | AGGGCAGGAGCCTGC[A/C]CTGCCATGGCCACCT | 57630 |
| rs368498494 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181666 | GTGTAAAAATCCTCC[C/T]AACACTCCTTCATCT | 57630 |
| rs368520755 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252313 | TACTTCTCTCTTTCA[A/T]GATTATAAAATATCT | 57630 |
| rs368553354 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264911 | GCCCCTTTGAAATAT[C/T]CTTCGCCTCTGCCCC | 57630 |
| rs368605207 | snp | A/T | 1.87415e-05 | 0.00306111 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116679 | CAACTATCTAATAGA[A/T]GCTGCTCACCAAAAC | 57630 |
| rs368665448 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169155566 | TTCGGATCACAGTCA[A/G]AACATCATCCTGAAG | 57630 |
| rs368672969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117889 | AAACATAGAACATTT[A/T]AAAAAATGAATGGAA | 57630 |
| rs368699044 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118342 | CCTTGCCTCAGATTC[A/C]GGTTTAAGATCTTAT | 57630 |
| rs368721358 | snp | A/G | 4.98335e-05 | 0.00499142 | missense | SH3RF1 | GRCh38.p7 | 4:169117724 | CCATGGTCACTCCCC[A/G]ACTTGTCTGGCCAGC | 57630 |
| rs368748546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232246 | AGGAATTTTAAAAGG[A/G]AATGATGTTCAAATC | 57630 |
| rs368856641 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260087 | GCATTCTTCCCAATA[A/C/G]AGTGAGTTAAGGAAT | 57630 |
| rs368889851 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264083 | GACCTTTAGGAGTAT[-/G]TCTACAGTCAGAGTA | 57630 |
| rs368897150 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144007 | ACACCGAAAGGTTTA[G/T]GTTAGAGTTAGGTCT | 57630 |
| rs368919060 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172868 | CAGTAATAGCACTTA[C/T]CCCTGGAAAGCAGGA | 57630 |
| rs368921565 | snp | C/T | 0.000159302 | 0.00892332 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156397 | AACAAGCACATTCTA[C/T]CTTTACCTTTGCAAA | 57630 |
| rs368925149 | snp | A/T | 0.000181401 | 0.00952196 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129998 | TGTGCCAGATTAACA[A/T]GACTAAAGACCTAAA | 57630 |
| rs368928071 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108805 | GGCAGTGCTGTATAT[A/C]CCTCTCTATCTCACC | 57630 |
| rs368957525 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195332 | TTGTCTTTTTCCCCC[C/G]ACTCTGGTTGCTTTC | 57630 |
| rs368971876 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160791 | CACACAGACTGCAGA[C/T]GATTAAGGATAAACG | 57630 |
| rs368993681 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221150 | CTCTAGTGAGCAAGA[A/G]TAATCCTCAATAGCA | 57630 |
| rs368998464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118575 | ATTCTCCTGTCTAAG[C/T]CTCCCGAGTAGCTGG | 57630 |
| rs369003831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133206 | AGCATCCAACTGCCT[A/G]TATCTAGATTTCATT | 57630 |
| rs369023379 | in-del | -/AA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131334 | CCAGGGGGTGGCACT[-/AA]AAAGAGTTTCTCCCC | 57630 |
| rs369028483 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149618 | ATTTACTTCAGGTTT[A/G]AAAGGGAAATTTGGA | 57630 |
| rs369040551 | snp | A/G | 1.64798e-05 | 0.00287047 | missense | SH3RF1 | GRCh38.p7 | 4:169117555 | CGGGCCTGGTTGACT[A/G]TCATTTGCCCCGTCA | 57630 |
| rs369067168 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167737 | TGAAAGAGGGTGTGA[A/G]GGAAATTTCTGAGAC | 57630 |
| rs369077367 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249720 | TTTCCAGCAAGCTGT[A/G]ACTCTTTAAGTAAAT | 57630 |
| rs369113560 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206216 | TTCACTGCTATAAAT[A/G]ACAGCACTTCTAAAT | 57630 |
| rs369145233 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170379 | TATACTGCATAAGAA[G/T]GTAACAGATCATGCT | 57630 |
| rs369189875 | snp | A/G | 0.000159223 | 0.00892111 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122189 | AGCAGCAGCAGCAGC[A/G]GCGGTGGCGCCTGGT | 57630 |
| rs369248651 | snp | C/T | 6.64993e-05 | 0.00576587 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116482 | GATGGCAGCAGTGTG[C/T]GTGGCTGAGCCTGGC | 57630 |
| rs369254694 | snp | C/T | 7.29022e-05 | 0.00603704 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116260 | AACAGTAAGTAAGTA[C/T]GGTCTTACTTTGCTA | 57630 |
| rs369267091 | in-del | -/GTTT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107973 | TTTGTTTGTTTGTTT[-/GTTT]TTTCAACTATTTCAA | 57630 |
| rs369327681 | snp | G/T | 5.53633e-05 | 0.00526104 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122276 | CAAAGTCTAGTATAG[G/T]AAAAACATAAAGAGA | 57630 |
| rs369336846 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233527 | TCAAAGTGTTTTATA[C/T]CTATTAACTCATTGC | 57630 |
| rs369375989 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199690 | GAGGTTCTGTCACAG[C/T]TTCCAATCCACTGGG | 57630 |
| rs369401314 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140985 | TTTGTTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 57630 |
| rs369415024 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103029 | CGGGTTCAAGCATTT[A/C]TCTGCCTCAGCCTCC | 57630 |
| rs369458741 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152858 | TGAGGAAGAAAAGGA[C/T]AGTTGAGGACAGGAA | 57630 |
| rs369468482 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232333 | CTAGAAACAGGTAGA[C/T]CAAGTCAGTGAGCTT | 57630 |
| rs369470487 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169762 | AGACAGGGTCTTACT[C/T]TGTCAACCAGGCTGG | 57630 |
| rs369529049 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160046 | TGGAAGCCTGCATGA[A/G]TTAATTGAAAATCCC | 57630 |
| rs369544746 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180641 | TATTTAATTGGTTTG[C/G]TCTTTGGTTGTTGCC | 57630 |
| rs369548011 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267832 | AGTGCTTACTGAAGA[C/T]ATTTGAAAAAAATAT | 57630 |
| rs369563554 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142311 | TATATGTATATATGT[A/G]TGTATATATTTATGT | 57630 |
| rs369574909 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116029 | ATGCAGCACTGAGTC[G/T]GGCAAGTAGTGGGCG | 57630 |
| rs369580467 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174308 | ACTCAAGCAATCCTC[A/C]CGCCTCAGCCTCCCA | 57630 |
| rs369588897 | snp | A/G | | | missense | SH3RF1 | GRCh38.p7 | 4:169122157 | GTGGATCCTGCCATG[A/G]GCCTCGGTCCCATTC | 57630 |
| rs369644903 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110021 | TGTAGCAAAACAAAA[A/C]AATACAAAAAAAAAA | 57630 |
| rs369673346 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252527 | CCATCTGGCACCTGG[A/G]TGCCAATAATTAGCA | 57630 |
| rs369682351 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138538 | AAACTGACTGATCAA[A/C]TCAGCACTCCTGTCC | 57630 |
| rs369717436 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241516 | TAAAGGCCTTAGGGG[C/T]TGAGAGCATCTGGAT | 57630 |
| rs369735991 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169321 | ATAACAAGAGACTGG[A/G]TGCAGCAGCTCACAC | 57630 |
| rs369740271 | snp | A/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095389 | TTGGTCAATTCTGAG[A/T]ACAAACTCATCTTAA | 57630 |
| rs369748127 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135479 | CAGCTTTGAACTAGA[C/T]TCTTTGACCTTTAAG | 57630 |
| rs369800637 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243018 | CTTTGAGAAACAGCA[C/T]TGCATGAAAAAGAAC | 57630 |
| rs369823693 | in-del | -/CA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269369 | CTAGGGAAAAAGTWC[-/CA]AMAGGAGCCAAGAAT | 57630 |
| rs369840641 | snp | A/G | 9.9519e-05 | 0.00705334 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122055 | TGAGGTTTGGACTTC[A/G]TTTAAATGAACACAT | 57630 |
| rs369918908 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227740 | GACCACATTATCTAC[A/C]ACCATAGAACAGTGC | 57630 |
| rs369926345 | snp | A/C/G | 5.31857e-05 | 0.0051566 | missense | SH3RF1 | GRCh38.p7 | 4:169268849 | TCCAGGATTGCACCC[A/C/G]AGGCTGCTGTCCGCC | 57630 |
| rs369929430 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205427 | ATAAGCATGGCAACT[C/T]TCCCAAGTGCTATCT | 57630 |
| rs369932424 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192853 | TGTGATATATATATC[-/AT]ATAGATGTGATATAT | 57630 |
| rs370011020 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190845 | ACTAGCTAACCAAAT[A/C]CAACAACATATCAAG | 57630 |
| rs370012969 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161036 | TTCCAAACTGCTGCT[A/T]TTCTTCTGTATCCTC | 57630 |
| rs370050156 | in-del | -/AATAT | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218196 | TGTGTAATATATGTA[-/AATAT]AATATAATATATAAT | 57630 |
| rs370091554 | snp | A/G | 0.000107896 | 0.00734414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136626 | CCGAGTTAAACTGCA[A/G]AAGCAACCAACAAAC | 57630 |
| rs370101312 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250316 | TGCTCATCTCTTGGG[G/T]TTAAAAAAAAAAAAG | 57630 |
| rs370142127 | in-del | -/CCCATC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263129 | ATCCCCATCCCCATC[-/CCCATC]TGTGCGAAGACAACA | 57630 |
| rs370153355 | snp | A/G | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094031 | TACATGACCTCGTGC[A/G]ACTCCACAAACTCTT | 57630 |
| rs370176763 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120540 | CTAGTAGAAAAATAC[C/T]GAAAATGGTGTTGTT | 57630 |
| rs370207223 | snp | A/G | | | missense | SH3RF1 | GRCh38.p7 | 4:169116519 | GGCGCAGGTTGTGGG[A/G]AGGCCAGCGAGTGAT | 57630 |
| rs370222729 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263817 | TTTCCCCTCTCAATA[C/T]TTCCTTCATTTCCTC | 57630 |
| rs370231425 | snp | A/G | 3.29587e-05 | 0.00405934 | missense | SH3RF1 | GRCh38.p7 | 4:169096569 | CAGTTTTCCCATTAC[A/G]TTGTAATGTGCCTTT | 57630 |
| rs370239648 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195642 | TTCTTCTCCATATTT[C/T]CTTTTACATATTTTC | 57630 |
| rs370246425 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155202 | AATGGAATAAACAGG[A/G]AATAGTGTAGGTGAC | 57630 |
| rs370306920 | snp | C/T | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169136584 | CTGGCACAGGAGGCT[C/T]ATCCCATTCTATCAG | 57630 |
| rs370336868 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135367 | TTTAAAGAAAAAAAA[A/C]CCACCATAGCTATAT | 57630 |
| rs370345159 | in-del | -/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226022 | ATGAATAAAGCTATT[-/TT]ATATATATAGCAACA | 57630 |
| rs370349084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212354 | CAGGCGTGAGCCACC[A/G]CGCCTGGACTATTTT | 57630 |
| rs370364149 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125252 | CTTGGGGCAGTCCTC[A/G]ACTTCCTTCCCTTGC | 57630 |
| rs370375710 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219231 | TAAGACAAGGTGCAA[A/T]AATGAGTATACATAC | 57630 |
| rs370389451 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222980 | AGGCACCATGTGGCA[C/T]CCCTCGTGGTTTGCC | 57630 |
| rs370395346 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176389 | TGACACAAACCTGTA[A/G]GTCATGCTAGCTACC | 57630 |
| rs370406883 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140423 | AAGCATTTGGTAAGG[A/G]GCTTTGATAAGACTT | 57630 |
| rs370410807 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239434 | CAGAAAACAAAAAAA[-/A]GACATCTGTGAAGGC | 57630 |
| rs370435633 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269322 | TCTAGAGTCATGGGG[-/A]AAAGGGGGAAAAGAG | 57630 |
| rs370468990 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252107 | GGCAATTCACTCTTG[C/T]TTCAGGTTGCACTTA | 57630 |
| rs370476040 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104738 | AAAACCCCATCTCTA[C/T]TGAAAATACAAAAAA | 57630 |
| rs370504039 | snp | A/G | 4.94401e-05 | 0.00497168 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117632 | TGATACCACAGCTGC[A/G]GGGACAACACTGGGA | 57630 |
| rs370560385 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214684 | GTCCATATATATGTG[-/TA]TATATATATAAGTAT | 57630 |
| rs370644998 | snp | C/T | 4.29277e-05 | 0.00463271 | missense | SH3RF1 | GRCh38.p7 | 4:169130150 | ACCCGGTGGTACTTA[C/T]ATGAACCTGCCGAGA | 57630 |
| rs370650230 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201803 | GTAAGTCAAAGATTT[A/G]CTATTAAAAATCCTG | 57630 |
| rs370686854 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202217 | TTCTTGGTGCCGGGA[A/G]GACAAGGAATAGTGT | 57630 |
| rs370688117 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182940 | CCCAAAACTACTAAA[A/G]GAAGACTGAAGTGGA | 57630 |
| rs370745143 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160918 | TCTGTGGATAAAATA[C/T]GTCTGGAGCCCATGG | 57630 |
| rs370748857 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181889 | TATTTCTCTTCATAG[A/T]CCTTACAGTCCATCA | 57630 |
| rs370756447 | snp | C/T | 3.44869e-05 | 0.00415238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117800 | GCCAAGACACAAACA[C/T]AGATGGAAAGCCCAG | 57630 |
| rs370762756 | snp | C/T | 1.6531e-05 | 0.00287493 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117695 | GGCAGGCCCTCCTGC[C/T]GTGGAAGGACTGACC | 57630 |
| rs370788875 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214509 | TGTTGAATCTATAGA[A/T]CAAGTTGGGAAAAAA | 57630 |
| rs370803489 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175974 | CATGATGGGATTGCT[A/G]CCTTTGTAAGAAAAG | 57630 |
| rs370803987 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170609 | AGGGCAGGGCTGGAG[C/T]TCATTCATCTTCATA | 57630 |
| rs370804487 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193402 | GTGTTAGCTTCCAAC[A/T]GACAATGCACAAGGA | 57630 |
| rs370865215 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235367 | ATAGCTAATACTCAT[C/T]CAACATTTACTATAT | 57630 |
| rs370890051 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271152 | CCCGGGAGCGGGCGC[A/G]GCACCTCTCGGAGCC | 57630 |
| rs370898195 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225367 | AGGCAATTGTTTGGG[A/G]GTTATCAGCAAGATG | 57630 |
| rs370899837 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247379 | AACATTAGAGCTATG[A/T]ACCTGGTCCAGGGGA | 57630 |
| rs370922445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142845 | CTTTGCAAAATGGTC[C/T]ATAATGGCAATGAGA | 57630 |
| rs370930736 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178261 | AGTAAACAAATAAAC[A/C]AAAAAAAAAAATTTT | 57630 |
| rs370932503 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154115 | TGCTTGGAAGTGCTT[A/G]TAGTTTCCCATTACC | 57630 |
| rs370964502 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102421 | TCCCCCAATTTAGGA[G/T]ATGAGCTTATAGGTA | 57630 |
| rs370970701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187133 | GCAACCTGCAACTCT[C/T]TTCCTAGTTTCTGGT | 57630 |
| rs370978579 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183079 | GGGAGTCTAAGGTGG[A/G]AGGATCACCTGAGGT | 57630 |
| rs371007155 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270236 | CCCAGGGCTGCACCC[C/T]CGCTCCCACGGCGCC | 57630 |
| rs371046953 | multinucleotide-polymorphism | AT/GG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204685 | CCCCCTGAGTAGCTG[AT/GG]ACTACAGGCATGCAC | 57630 |
| rs371090000 | snp | G/T | 1.75761e-05 | 0.00296441 | missense | SH3RF1 | GRCh38.p7 | 4:169136400 | GAGCTGATGAGGACA[G/T]GGGGGCTGATCTCCA | 57630 |
| rs371110983 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175156 | GCATCAGCAAGTCTG[C/T]CAGCTTTGACTTCAG | 57630 |
| rs371149865 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212768 | ATGCCATGGTTTTGG[-/A]AAAAATGTTTAATCA | 57630 |
| rs371166197 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178260 | AAGTAAACAAATAAA[-/C]AAAAAAAAAAAATTT | 57630 |
| rs371170972 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136011 | CCCAAAGCAGTACTG[C/T]GAGAAAGTTCTGTAA | 57630 |
| rs371199524 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240592 | GAGTTTTCTTCTTTA[A/G]CAAATAAATAAATTG | 57630 |
| rs371220815 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180711 | CACTGTGAAATCGTT[-/A]AAAAAAATTATATTT | 57630 |
| rs371246786 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113625 | GAATCTCAATGTGGC[A/T]TCTGGTGAGTTCTCC | 57630 |
| rs371278882 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095046 | ATGACTGCGTGGCAC[C/T]GTAATGAAATCGGTG | 57630 |
| rs371323427 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119344 | TGGTCAGGCCTCAAG[C/T]GATCAACTCCTGACC | 57630 |
| rs371326422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157940 | AATGGGGTCTCGCCA[C/T]GTTGGCCAGGCTGGT | 57630 |
| rs371342211 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122592 | AAGTATGGACTTGGA[A/C]AAGGATCCAAATGCC | 57630 |
| rs371376047 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240953 | AAAACTGCCCAGGCC[A/G]GGCGTGGTGGCTCAC | 57630 |
| rs371384104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221636 | CATATAAACACTATG[C/T]TCCTTATAACATACC | 57630 |
| rs371388502 | in-del | -/TCCACAAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241573 | TCAGCACTCCTGAAC[-/TCCACAAC]TCCACCAGAGGAGAC | 57630 |
| rs371396089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192707 | TACAGCAGCACAATT[C/T]GCAATTGCAAAAACG | 57630 |
| rs371472801 | snp | A/C | 1.65422e-05 | 0.0028759 | missense | SH3RF1 | GRCh38.p7 | 4:169116382 | GGCCACTGGGCTCAG[A/C]CTCCAGAGAAGCACT | 57630 |
| rs371510086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147281 | GATTACCAGATGTAG[A/G]GATACTATAAAAGAA | 57630 |
| rs371520528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109549 | AAAGATGCTGTCCTA[C/G]TTCCAAGGAACCATG | 57630 |
| rs371569802 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180530 | AGAAAAGAGATGGCC[A/G]TTTAGTATGCAGACT | 57630 |
| rs371605339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111733 | TTGTTATACTGATGA[C/T]GGTGGAAAACATTAG | 57630 |
| rs371675597 | snp | C/T | 1.64817e-05 | 0.00287064 | missense | SH3RF1 | GRCh38.p7 | 4:169120898 | CTTTGAACCAGCCAT[C/T]CTGGCAGCGCTCAAA | 57630 |
| rs371702089 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101914 | AATATAAAGAAGCTC[C/T]ACAGACTTCCAATGC | 57630 |
| rs371801632 | in-del | -/AAGA | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109355 | TCTAAAGTGATTAAG[-/AAGA]AAGATGACTTAATTC | 57630 |
| rs371822602 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203828 | ATTCTACAAAATTAT[G/T]TATTTAGAAGCACAT | 57630 |
| rs371823137 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236613 | TTCGTAGTGTTGCTA[C/T]GAGAATTAAATAAGT | 57630 |
| rs371828703 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255036 | TTGCAAGGACAGGAA[C/T]TTATGTTTAACAGAA | 57630 |
| rs371854925 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252565 | CTGATTGCCAGATAA[C/T]AGTCAACTGACCAGG | 57630 |
| rs371905887 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149414 | CTTGTATCAAGTGGA[C/T]AGCATTCAGAAGATA | 57630 |
| rs371907236 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148479 | GAAAAAGAATGGAAG[A/G]ATATTTACCAAAATT | 57630 |
| rs371929990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132640 | TCATGGAACTGCAAA[A/G]ATTAGTTGTCTCCTC | 57630 |
| rs371944259 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117939 | GAATAGAAAATTCAA[C/T]GTAATGATGGCTGAG | 57630 |
| rs371985673 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171336 | ATTGTTCTTTGCTCA[A/G]TTAAATTATGTTGAG | 57630 |
| rs372014313 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102824 | GTCAACACACTTCAA[C/G]GTTCATCCTTTCTTA | 57630 |
| rs372016638 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137899 | GCTTGTCTCATCTAT[-/A]AATTAGTAAGATAAA | 57630 |
| rs372028417 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182786 | TATGAGAATAATTTA[-/C]TCTGTTTCCTTGAAG | 57630 |
| rs372069906 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144193 | TGAACATGAGTTATT[C/G]TTACTATTCAGAGTC | 57630 |
| rs372073921 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203208 | TCACAGAGTATCAAC[C/T]CATAACTCAAAGCAT | 57630 |
| rs372094474 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176969 | GACAGGGTTTCGCTA[C/T]GTTGCCCGGGTTGGT | 57630 |
| rs372110813 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238973 | TTTCCGCCCCCCCCC[-/C]ACCCCTTGCCCTTTT | 57630 |
| rs372130096 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188651 | AAAAAGCCCACATGT[A/G]AAAACATCGACACAC | 57630 |
| rs372136743 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095790 | GTTTCAGTCACTTCA[C/T]TCTAGGAAAATTAAA | 57630 |
| rs372148954 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215958 | ACTGGCACACACCAC[C/G]ATGCCTGGTTAATTT | 57630 |
| rs372163983 | snp | C/T | 1.6537e-05 | 0.00287545 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169155489 | ATTTACCTCAACATA[C/T]GAAATTGGAAATATT | 57630 |
| rs372167009 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103961 | TACATTCTCCATGTT[C/T]CCTATCTGATGTGCA | 57630 |
| rs372182820 | snp | G/T | 3.60198e-05 | 0.00424366 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156379 | TAGAGCTGGCAAACA[G/T]AAAACAAGCACATTC | 57630 |
| rs372198241 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176631 | CTGCAACCTCAGTTT[C/T]CCACGTTCAAGCGAT | 57630 |
| rs372199743 | snp | A/G | 6.96355e-05 | 0.00590024 | missense | SH3RF1 | GRCh38.p7 | 4:169116562 | CAGATGCAGGGCTGA[A/G]GCCGGCGGCATTCTG | 57630 |
| rs372209433 | snp | C/G | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169107090 | ACCGCTCCCTGGAGA[C/G]GAAGCTCTGCACTGC | 57630 |
| rs372209447 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219058 | AACTCCTTAATAACC[A/C]TTTCTTACATAACAG | 57630 |
| rs372228006 | snp | C/T | 0.00366534 | 0.0426525 | missense | SH3RF1 | GRCh38.p7 | 4:169122191 | CAGCAGCAGCAGCGG[C/T]GGTGGCGCCTGGTGG | 57630 |
| rs372229455 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194892 | TGTAACAAATGACAT[C/T]GAGCACCTTTTCAAA | 57630 |
| rs372236934 | in-del | -/CAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263005 | AAACAAACAAACAAA[-/CAAA]ACCCACCTTTTCCGT | 57630 |
| rs372273245 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188750 | AAATGAAAAGCTTTA[C/T]GCAGAAGTGGCCAAA | 57630 |
| rs372294774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260572 | AACTCAAGAACAAGA[C/T]GGACCTCCAGCTAAA | 57630 |
| rs372349520 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268360 | ATTCATAAAACCAAT[A/G]GAATGATTCTAAGCA | 57630 |
| rs372368907 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170963 | ATAAATACAGTAATT[A/G]AAGGAAATTTTCCTG | 57630 |
| rs372373147 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106623 | AGTAGAGAAAATAAA[A/G]GAAAAGGAAGGCTGG | 57630 |
| rs372381759 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233273 | AAAAAAAAAAAAAAA[-/A]CCGTGGTTTACTCAG | 57630 |
| rs372412318 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211407 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGT | 57630 |
| rs372423509 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167341 | CTAAAAAATGTGGAG[C/T]AACTAGAATTTACAT | 57630 |
| rs372441375 | snp | A/G | 0.0158469 | 0.0875917 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096071 | CATTCACTCTATGTC[A/G]AAACGAATCTCTTGC | 57630 |
| rs372454228 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226846 | TAAATCTAAATTGTA[C/T]TACCTCAGTCACCTA | 57630 |
| rs372462708 | snp | A/C | 0.00115583 | 0.024012 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121039 | GTAACAGACAAATCC[A/C]AAGATGCTCAAAATT | 57630 |
| rs372468295 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163536 | AGGTAGGACGAAAAC[C/T]AGCAAACTATAACCA | 57630 |
| rs372569534 | snp | C/T | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169156456 | TCTTTCACTTCAAAG[C/T]CATAAAGTGCTTTGC | 57630 |
| rs372580230 | in-del | -/A | 0.0551013 | 0.156571 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094785 | ACATTGTTTTTTTTT[-/A]AAAAAAAAGGTTAAT | 57630 |
| rs372605650 | in-del | -/ACAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255623 | CATACATACACACAT[-/ACAC]ACACACACACACACA | 57630 |
| rs372623278 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233509 | TCACAGGACAGGTAC[G/T]TTTCAAAGTGTTTTA | 57630 |
| rs372629197 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232276 | CACATTTGGGAAAGA[-/C]CCGCCATAGCAATGT | 57630 |
| rs372646087 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | SH3RF1 | GRCh38.p7 | 4:169117590 | CAACAAGACCTTAGC[C/G]TGAGGACTTGTCTGG | 57630 |
| rs372655462 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273078 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCACTCTTA | 57630 |
| rs372682166 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100371 | TTTAAGACTGAGTTT[C/T]GCTCTTGTCACCCAG | 57630 |
| rs372739666 | in-del | -/TG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202490 | ATCTGAAGGAGGGGA[-/TG]TGGTTCCTTTTAAAG | 57630 |
| rs372739765 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192644 | CTACTGGGTATCTAC[C/T]CAAAGGAAAAGAAGT | 57630 |
| rs372741536 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115222 | ATTTCAAGTCTTACC[A/T]CTCAAGGAACCATGC | 57630 |
| rs372766124 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241581 | TCCTGAACTCCACCA[C/G]AGGAGACAGTGAGAA | 57630 |
| rs372774900 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252642 | CTATCTTTAACCAAC[C/G]TATTCTATTTTTTTG | 57630 |
| rs372783209 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205592 | GTTCTTTTTTCCCAT[A/T]TGCTCTCATTAAAGT | 57630 |
| rs372806555 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225297 | GGCCAACTTCACAGG[G/T]AGGAAAAGTCAGCTG | 57630 |
| rs372821620 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267836 | CTTACTGAAGACATT[C/T]GAAAAAAATATTCTC | 57630 |
| rs372822322 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255242 | AAAATCAGTACGTGA[A/C]TATTTTAACTATAAA | 57630 |
| rs372824086 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212355 | AGGCGTGAGCCACCG[C/T]GCCTGGACTATTTTC | 57630 |
| rs372829457 | in-del | -/A | 0.0337553 | 0.125452 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186826 | CTGGCTAACACGGTG[-/A]AAACCCCATCTCTAC | 57630 |
| rs372839460 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191812 | GCCTTTTTCAACAAA[C/T]GGTGCTGTGATAATT | 57630 |
| rs372867196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170405 | ATGCTAGCTGTATTC[C/T]TACTAACGAAAAATT | 57630 |
| rs372894630 | snp | A/G | 0.000116637 | 0.00763575 | missense | SH3RF1 | GRCh38.p7 | 4:169117741 | CTTGTCTGGCCAGCT[A/G]TAGACATAGGGACTT | 57630 |
| rs372906095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190681 | CTATTGACACTATTC[C/T]GCAAGACAGAGAAAG | 57630 |
| rs372925861 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113060 | ATCTGGTGAATCTGG[C/G]ATGAGGGTCAACTGA | 57630 |
| rs372950867 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206243 | AAATATTTGAAAATG[A/G]TATCTTAGCATGCCA | 57630 |
| rs372954313 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109104 | GATGACATGCAAAAG[A/T]ATAATGTCCAGTAGC | 57630 |
| rs372954556 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249791 | TGAGGCATATGACTG[A/C]AGTCATGTTTATGAG | 57630 |
| rs372978936 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268904 | GCTACAATTAGCCAC[A/C]GTGCTGCTCTGAGAC | 57630 |
| rs373053024 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211689 | AGGGGGGAAGTGTTA[C/T]GAACAATTAAAGCCT | 57630 |
| rs373055867 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249423 | GCCCTCACCAGATAA[C/T]TGAACCTACCAGCAC | 57630 |
| rs373055882 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256041 | CCAAAGTTCTGAGAC[C/T]ATAGGCGTGAGCCAC | 57630 |
| rs373076612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258040 | GTTTGTCCTAAATGT[C/T]TGATATCAAAGTTGG | 57630 |
| rs373088831 | snp | C/T | 7.25953e-05 | 0.00602432 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136290 | TGTGGGTGAGCTCTT[C/T]TTATATAACACTTGT | 57630 |
| rs373111379 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196807 | TTTCATTTTAATAAG[C/T]TGTTCCTTTACTATA | 57630 |
| rs373121688 | snp | A/C | 3.45865e-05 | 0.00415837 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107176 | AGTGGAGGCGCCAGA[A/C]AGCAACTTCAACAAA | 57630 |
| rs373160030 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187383 | CTTTTTGTGGAGATG[C/G]GGTCTCTATATTACC | 57630 |
| rs373171890 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237304 | AGCATTAATTTTCCA[A/G]AGGTGACTTTCACCA | 57630 |
| rs373172174 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165446 | CAGCACTTTGGGAGG[C/T]TAAGGCAGGCAGATC | 57630 |
| rs373180447 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119276 | GCCTGGCTAATTTTT[-/G]TATTTTTTTTTTTTT | 57630 |
| rs373222611 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152868 | AAGGATAGTTGAGGA[C/T]AGGAAGAGAGGGCAA | 57630 |
| rs373255955 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269343 | GGGAAAAGAGAACAT[A/G]AGTGTTGTTATCTAG | 57630 |
| rs373274002 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243287 | GGAGGTCGAAGCAGG[C/T]GGACCACCTGAGGTC | 57630 |
| rs373300676 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245200 | AATCAACTTATTAAA[C/T]ACAACTTTAACGCTA | 57630 |
| rs373309304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244726 | TTAAATTGCGCATGT[A/G]TTACCAAAACACAAT | 57630 |
| rs373321746 | in-del | -/GGC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101672 | TTTGTTTAAAAAAAA[-/GGC]AAAAAAAAAAAAAAA | 57630 |
| rs373332263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202073 | ATTAAATGAGAGACA[A/G]TGCTGTCAGCTTAAA | 57630 |
| rs373371466 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260017 | TAAGCAATATACTAG[A/C]GAGGGGATAGATTAA | 57630 |
| rs373399323 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264035 | CCAGGACTGAAGGGA[C/T]TGGCAGTGGACCGAG | 57630 |
| rs373408058 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183349 | TCAATGGCGTGATCC[G/T]GGCTCACTGCAACCT | 57630 |
| rs373510705 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169353 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCA | 57630 |
| rs373660112 | multinucleotide-polymorphism | AA/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117424 | ATGTTGTTCATTATT[AA/TT]AATTACATCTACATT | 57630 |
| rs373686748 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109440 | GGATGTCTTATCATC[A/T]TCAACTGATGCTGAC | 57630 |
| rs373720452 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126874 | GGGATTATAGGCATG[C/G]GCCATCACACCCAGA | 57630 |
| rs373748260 | snp | A/G | 1.65581e-05 | 0.00287728 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121002 | TACCTAGAATAGAAA[A/G]TAATATTTGATTTCA | 57630 |
| rs373774899 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163941 | AAGGCCAAGATCAAT[G/T]ATCTGATTCTTGTGT | 57630 |
| rs373862179 | snp | G/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271378 | ATGGAGCCACCGGAC[G/T]GGAAGGCGGCGGGAG | 57630 |
| rs373862892 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144398 | AATAGGCAAAGACTT[C/T]TGTGTTGGGAATAGG | 57630 |
| rs373910722 | snp | G/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272285 | AAACCATTCAAGACA[G/T]AAGGATCACATAAGC | 57630 |
| rs373918064 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226446 | GAAAAGCAAAATACA[C/T]GGAATGTTATAATGA | 57630 |
| rs373940689 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103112 | TTTTTTTTTTTTTGT[A/T]TTTTTAGTAGAGATG | 57630 |
| rs373949565 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237871 | ATCAATTTATGATTT[-/C]CCCCCCCGCTCCACA | 57630 |
| rs373959180 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152566 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAC | 57630 |
| rs373981246 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260963 | AGCTAAGGATCCCTA[C/G]AGAGGTTGGTACTCC | 57630 |
| rs373998438 | snp | A/G | 1.65625e-05 | 0.00287766 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122071 | TTTAAATGAACACAT[A/G]AGCAGTAACAGACGA | 57630 |
| rs373999819 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192542 | CACTGCTGATGGGAA[C/T]GTAAACTAGTACAAC | 57630 |
| rs374031777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100157 | ACCCTCTGCCTCACT[C/T]GGATTATGCTTTTCT | 57630 |
| rs374059914 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222292 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 57630 |
| rs374075713 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099297 | TCTCACTATATTGCC[C/G]AGGCTGGTCTTGAAC | 57630 |
| rs374119558 | snp | C/T | 4.94564e-05 | 0.0049725 | missense | SH3RF1 | GRCh38.p7 | 4:169117658 | TGGGACTCCCAGCCA[C/T]GCCATTTCCCTGGAG | 57630 |
| rs374151855 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250298 | TATGGTTTGGAATCA[C/T]ACTGCTCATCTCTTG | 57630 |
| rs374188258 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130689 | TAGACATGCTTAGAG[C/T]GGGCAATTACTTATA | 57630 |
| rs374197850 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230632 | GGGAGGCCAAGATGG[A/G]CAGATCACCTGAGGT | 57630 |
| rs374206465 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138070 | AGACTTCTTCCGATA[C/T]GTGTTTAGGGATGAA | 57630 |
| rs374212872 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182986 | TAGGGGTTTGAGACC[C/T]GGCTGAGCAACATAG | 57630 |
| rs374216374 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157747 | TTTTACTTTTTTTTT[C/T]TTTTTTTTTTTTAAG | 57630 |
| rs374286270 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139221 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 57630 |
| rs374298503 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132822 | TCCTAAGTGTGGTCA[A/G]AGGAGGAGACAAAAC | 57630 |
| rs374311537 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174309 | CTCAAGCAATCCTCC[A/C]GCCTCAGCCTCCCAA | 57630 |
| rs374311814 | snp | A/G | 0.000297924 | 0.0122014 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117495 | AAGCCCTTTATCCTG[A/G]TATGTTCTGGCCTGG | 57630 |
| rs374324259 | snp | A/C/T | 0.000115732 | 0.00760621 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122084 | ATAAGCAGTAACAGA[A/C/T]GACACGCTCACTTAC | 57630 |
| rs374356535 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183174 | GCATGGTGGAAGGCA[A/C]CTGTAATCTCAACTA | 57630 |
| rs374375038 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221626 | TTCATTTTAACATAT[A/G]AACACTATGCTCCTT | 57630 |
| rs374382825 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100601 | CACCTTGGCCTCCTT[C/T]AAGTCTCTTCCTGTC | 57630 |
| rs374453232 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195514 | TCTATTCAAATACTG[C/T]GGTGCTCCACTTTAG | 57630 |
| rs374478370 | snp | A/G | 9.919e-05 | 0.00704167 | missense | SH3RF1 | GRCh38.p7 | 4:169117696 | GCAGGCCCTCCTGCC[A/G]TGGAAGGACTGACCA | 57630 |
| rs374496108 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148569 | ATTGTAGAAATAAAA[C/T]CATTAAAAATATCCT | 57630 |
| rs374497138 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251310 | AACAAATACACGTAA[A/C]GTCATGTATACACGC | 57630 |
| rs374504878 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179049 | CCAATCCCTGAACCC[C/T]ATGAATCTGTTGCCT | 57630 |
| rs374513980 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243711 | TTAAATCTGTCCTCA[A/G]CAGATTCTTGCACTG | 57630 |
| rs374524447 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266283 | GAACATAACTAATAA[A/G]CTGAAGCAACATTCC | 57630 |
| rs374537074 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229818 | TGTCAAATCAATGCC[A/C]AATTGCAACTACAAT | 57630 |
| rs374538806 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169096573 | TTTCCCATTACGTTG[C/T]AATGTGCCTTTGAAC | 57630 |
| rs374558381 | snp | C/T | 1.68196e-05 | 0.00289992 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116317 | GTTCCCACAAGCTGA[C/T]GAAGCACTGTCAGGA | 57630 |
| rs374589276 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118180 | CCTGGCTTCCTACTT[A/G]CCTCCAGCTCCACAT | 57630 |
| rs374594344 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143603 | GGCCCACATTTCTGA[C/T]GCCTCCTGGGTCCTG | 57630 |
| rs374595744 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200535 | TCAGTAAGAATGAAC[A/C]ACAGCTCACAACAGG | 57630 |
| rs374604476 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160676 | TAGAAAGCCAGTTTG[G/T]GTCAAGTTTCTAAAA | 57630 |
| rs374628496 | in-del | -/TG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106087 | TTTTAACAGTATATA[-/TG]TGTGTGTGTATATAT | 57630 |
| rs374640828 | snp | A/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271477 | GCTGGGAGCCCTGGA[A/C]GGACCCTTCCTCCCC | 57630 |
| rs374659148 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191359 | GAAAGACCTCTACCA[A/G]GGAAACTACAAAACG | 57630 |
| rs374676475 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133635 | ATATAAAAACTAGCC[A/G]GGTGTGGTGGTGGCG | 57630 |
| rs374697186 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096163 | AAATCATAATCCAAA[G/T]AACGTATCTATTATA | 57630 |
| rs374725519 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137238 | TATCAGCTATCATCC[C/T]ATGTGCACGTACTTT | 57630 |
| rs374744282 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166013 | ACTGTAAGTTTTATA[A/G]GGGAAACAAGAAATT | 57630 |
| rs374744664 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172854 | TAAAGAATAGAAAAC[A/G]GTAATAGCACTTACC | 57630 |
| rs374751652 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138301 | ATGGAGGGGTAGGGT[C/T]CTCTTTCCTGCACAG | 57630 |
| rs374783049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111299 | TAGTTCTGTCACCCA[A/G]GCTGGAGTGCAGTGG | 57630 |
| rs374810853 | snp | C/T | 1.6507e-05 | 0.00287284 | missense | SH3RF1 | GRCh38.p7 | 4:169156474 | TAAAGTGCTTTGCAC[C/T]GAGGTGGGGGCTGAG | 57630 |
| rs374824375 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097915 | CTCAACATCTCTATG[C/G]AGAGGAAACACATGG | 57630 |
| rs374843599 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141825 | TGCTTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT | 57630 |
| rs374852663 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104893 | GCAACAGAGTGAGAC[G/T]CCCATCTCAAAAAAA | 57630 |
| rs374900640 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216972 | CCTGAGCAACATGGC[A/G]AAACCCCATCTCTAC | 57630 |
| rs374906297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121119 | TATAATCCTTTAATC[C/T]ATAAGTAGCACTGAC | 57630 |
| rs374907887 | snp | A/G | | | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136396 | GCTGGAGCTGATGAG[A/G]ACAGGGGGGCTGATC | 57630 |
| rs374915001 | snp | C/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116948 | GATGGTATTCTACAG[C/G/T]GTCAAGCGATGTCTC | 57630 |
| rs374917176 | snp | A/C/G | 6.62662e-05 | 0.00575581 | missense | SH3RF1 | GRCh38.p7 | 4:169122163 | CCTGCCATGGGCCTC[A/C/G]GTCCCATTCCAGCAG | 57630 |
| rs374940186 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129506 | TCTGTAGGATGTCAT[A/G]TTTTCAGAAGGGAAA | 57630 |
| rs374988981 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262180 | ATTAGCAAATCATTG[A/C]ATCTCCAGAGCATGA | 57630 |
| rs374997163 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236887 | ATAAAACCCAGGATA[C/T]CATCTGTTACAAAAT | 57630 |
| rs375022459 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200833 | CCAGAATAATTAGTC[-/C]ATCCCAACTGAGATG | 57630 |
| rs375028214 | snp | A/T | 3.81847e-05 | 0.00436931 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107233 | AATAATGAGCCTTAG[A/T]TGGAGAATGACAGTA | 57630 |
| rs375083700 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214135 | AGGGAAGTGTTTGGG[G/T]CATGGGGGCGCACCT | 57630 |
| rs375135471 | snp | C/T | 1.81694e-05 | 0.00301403 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136645 | CAACCAACAAACCAA[C/T]ACAAGAAGGTTAAAC | 57630 |
| rs375178955 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234324 | CACCCTCCCCACCCC[A/C]CAAAAAGAATTATTC | 57630 |
| rs375191469 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148589 | AAAAATATCCTTTAC[A/G]TAAGATATGGCTCTA | 57630 |
| rs375195196 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176771 | GTCTCGAACTCCCTG[A/C]CTCAGGCAATCCACC | 57630 |
| rs375198549 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195331 | TTTGTCTTTTTCCCC[C/T]CACTCTGGTTGCTTT | 57630 |
| rs375218261 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160416 | TAAATAGACCAGTGG[C/T]AAGGAGAAAGCTTAC | 57630 |
| rs375219999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118748 | AGGTTTGAGCCAACG[C/T]GCCTAGCTGGTGTAT | 57630 |
| rs375234223 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193435 | CCACCCCCAGAGAGT[A/T]ATTTGGGGGATATTT | 57630 |
| rs375294112 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095103 | GATATAAAAAGACAG[A/G]CTCTTCTGGATCCTG | 57630 |
| rs375319495 | snp | G/T | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094092 | TGTTAGTTGCAGAGG[G/T]AAAATGTGTCATAAT | 57630 |
| rs375342068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148382 | GAGTGTTTATTAGAC[A/G]GTCATAAAAACTGAT | 57630 |
| rs375350457 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113442 | GACACCAAAGCACTT[G/T]GCAGACCATCTGGGA | 57630 |
| rs375404425 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204260 | AGTACTGTAGTTTAC[A/G]TTTCAGGTGTGCATC | 57630 |
| rs375414779 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263475 | ACAGGTGCTTGTTCA[C/T]AGATGGATGTCAAAG | 57630 |
| rs375418943 | snp | C/T | 1.75925e-05 | 0.00296579 | missense | SH3RF1 | GRCh38.p7 | 4:169116568 | CAGGGCTGAGGCCGG[C/T]GGCATTCTGTACCTG | 57630 |
| rs375422173 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217316 | AATTGTGGGAAGAGC[A/G]GACGGACCTGGGAAG | 57630 |
| rs375437473 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173449 | TTAAAAAAAAAAAAG[C/T]AGCAAAAGAACACAG | 57630 |
| rs375447699 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250706 | GATGGGGGTAGGAGG[G/T]ATTAAACAAATAAAT | 57630 |
| rs375449793 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098569 | CTTTGGCACAGGGAC[C/G]AAATTACTACCCAAG | 57630 |
| rs375451149 | snp | C/T | 3.78544e-05 | 0.00435038 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106832 | AGTTTTTTCCTGGAA[C/T]GAAGTTGAACTTACC | 57630 |
| rs375478546 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169155531 | TGCCAGCATTCCTTC[A/G]GCCCAGTTTTCATCC | 57630 |
| rs375504815 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135846 | AAATTAAATGCTTCT[G/T]TCTGTCCTTGCTCTT | 57630 |
| rs375544493 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165398 | AAAGAGGTTGGGTAA[-/C]CAGCCACATGCAGTG | 57630 |
| rs375557542 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198675 | AAGCAAAACGATTAC[G/T]AAAGAGAATAAATAA | 57630 |
| rs375658732 | snp | C/T | 0.000313746 | 0.012521 | missense | SH3RF1 | GRCh38.p7 | 4:169136481 | GAAGTGAAGGAGTGC[C/T]GCTTTTTGGTGTTCT | 57630 |
| rs375665321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190287 | TGAAACAAAAAGCTG[A/G]TTCTTTGAAAAGATA | 57630 |
| rs375672416 | in-del | -/ATAA | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173028 | TCTAATACACTTGCT[-/ATAA]ATAGAGTATCTTGTT | 57630 |
| rs375683601 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229426 | TTGTGTCCCAAATTG[C/T]GTTCCTTAGAACACC | 57630 |
| rs375708953 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210369 | TATGACTACTTGGCT[C/T]ATACTCCAGATATGC | 57630 |
| rs375778951 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123019 | TTCTTTAGGGTCTGT[A/G]TACTGAAACTCTTGG | 57630 |
| rs375856778 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230960 | ATAAACAATAGGCTC[A/G]AAAGGTTGAAAAACA | 57630 |
| rs375863935 | snp | C/T | 8.4081e-05 | 0.00648332 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107005 | CACTGCAGTCGTGAC[C/T]GGTCCGTCCCCGTCC | 57630 |
| rs375875790 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095217 | CATCCTTGATGTCTG[C/T]CTGCTGGGAGGACAT | 57630 |
| rs375887944 | in-del | -/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273057 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT | 57630 |
| rs375887970 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213173 | AATGAGAATTCCTGT[G/T]GATCCACATTCTCAC | 57630 |
| rs375902004 | in-del | -/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273056 | ATTTTCTTTTCTTTT[-/C]TTTTTTTTTTTTTTT | 57630 |
| rs376002464 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098536 | AAAGGTAAGTGGCTG[C/T]TTGAACAACCTGAGC | 57630 |
| rs376019289 | snp | A/C | 0.000132304 | 0.0081323 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116425 | GGAAGTCAGTGGAGC[A/C]GCTGCTGCACAGGCC | 57630 |
| rs376025679 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206559 | AGTCCATCAAGGGAT[A/T]CACTTTAAATAAGTG | 57630 |
| rs376038683 | snp | C/T | 0.000286944 | 0.0119745 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130021 | GACCTAAAAGAGAAA[C/T]AAAAATGGGAGAAAC | 57630 |
| rs376042344 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151274 | AACAAATAACTGGAA[A/C]TACTCACAGAGAGAA | 57630 |
| rs376049005 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153165 | GTTAGGTTCTTTTAT[G/T]TGATTATTACCATGC | 57630 |
| rs376052017 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129936 | AAGATAGATACCCAC[C/T]TCACCTAACAAGTAT | 57630 |
| rs376058568 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173002 | AATGTGTAAGAAAAA[A/G]TGTGTGAAATTCTAA | 57630 |
| rs376063611 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185992 | CTGCTTCCTCCCCAG[C/G]AATCCTCAGAAACAC | 57630 |
| rs376070765 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225387 | TCAGCAAGATGGTGA[A/C]CCCTAAAGTCACGAG | 57630 |
| rs376115480 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188274 | GAAAAACAACTTTCC[C/T]GTGGCCCATTCATTC | 57630 |
| rs376131621 | snp | G/T | 1.65302e-05 | 0.00287486 | missense | SH3RF1 | GRCh38.p7 | 4:169117693 | TGGGCAGGCCCTCCT[G/T]CCGTGGAAGGACTGA | 57630 |
| rs376149479 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157281 | TGGATACAGCAGTGA[A/G]TGAACAGTCACAGTA | 57630 |
| rs376159664 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258522 | GGAATGAAAATAATA[C/T]GATCTACCAAAGATG | 57630 |
| rs376179416 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233822 | CATTTCATTAAGAGA[C/T]GTAATTGAAAATCTA | 57630 |
| rs376216828 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229147 | TCTGTTTTGAGACAG[A/G]ATCTTGTTCTGCGGC | 57630 |
| rs376218061 | in-del | -/CT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219982 | ACAAACTAGCGTGTG[-/CT]GTACTCTAAATTACA | 57630 |
| rs376269905 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229287 | TTTTGTCAAACTTAA[C/T]CCAATTCTCCAATAC | 57630 |
| rs376272239 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211839 | CATCCCAAGTCACCA[G/T]CTGGATAACTGCACT | 57630 |
| rs376306884 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161957 | GGCTGAGACAGGCGG[A/C]TCACTTAAGTCTAGG | 57630 |
| rs376308285 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212385 | CTAATTTCTAAAAGA[G/T]TCTCTGAAATATTTA | 57630 |
| rs376309391 | in-del | -/AGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209331 | TATAGAAAAAGAGTG[-/AGTG]TCCTTTCAGCCAACT | 57630 |
| rs376319658 | in-del | -/AA | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094925 | TAAAGGAAAAAAAAA[-/AA]GATGAAAGGGTTTAT | 57630 |
| rs376321292 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105146 | TTCAAGTCGGCAACA[C/T]AGAAAATGCTACCAA | 57630 |
| rs376322003 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195430 | TATTTATCATTCTTG[G/T]AGTTCACAGGATTTC | 57630 |
| rs376369416 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128384 | CCTTCGCCAAGCAGC[C/T]GTACTATCAAGAAAG | 57630 |
| rs376428175 | in-del | -/CT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204435 | ACTTAAACCAAGTTT[-/CT]AACACTCCACATATA | 57630 |
| rs376536516 | snp | A/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273046 | AGTCACACCCATTTT[A/C]TTTTCTTTTCTTTTT | 57630 |
| rs376565444 | snp | C/G | 1.64822e-05 | 0.00287068 | missense | SH3RF1 | GRCh38.p7 | 4:169096644 | CTTCTTTAAGTTCAA[C/G]TTCTGCCTCACTCTG | 57630 |
| rs376570020 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228745 | CCTACTGCAGCATGG[A/T]ATCATCCATCAGTAC | 57630 |
| rs376631943 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224613 | GTGAACCACCACCAC[C/T]GACCTCTAATTTCTA | 57630 |
| rs376654092 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184905 | GTCTGTGAGATAAAC[A/G]GTTTTATTTCCTGAT | 57630 |
| rs376691242 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171982 | GCTATTTTTATGGGA[C/T]TTGGGGAATTAATTA | 57630 |
| rs376723377 | snp | C/T | 1.65075e-05 | 0.00287289 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268919 | AGTGCTGCTCTGAGA[C/T]CTTAATGCATTTGTG | 57630 |
| rs376729130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225265 | CTTCGGCTTCAGACA[C/T]ATTAGGTTTGAATGC | 57630 |
| rs376754305 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239580 | CGTTAAGGTTTCAAA[A/C]ATTTAACCATTCTAC | 57630 |
| rs376777943 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131823 | GGTTGCTGTCCTCAA[C/T]CATTGATTGTGGGCC | 57630 |
| rs376789944 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103739 | AAATAAATACTATCA[C/T]CATCACTGTATGAAA | 57630 |
| rs376797334 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183989 | GTTTTTTAAAGCAGT[A/G]ATAGCTTATGTCATT | 57630 |
| rs376812748 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144863 | AAAAGTCATGGGGAT[A/C]GTACTAGTTGGTGAT | 57630 |
| rs376859583 | snp | A/G | 3.31235e-05 | 0.00406948 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121005 | CTAGAATAGAAAATA[A/G]TATTTGATTTCAGGT | 57630 |
| rs376863351 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201521 | ATGTTTCAGGAATGC[C/T]AAAGGAGACCAGGCA | 57630 |
| rs376892090 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124914 | CTTTCATTCACCCGG[A/C]GGTGACCTGGAGTCC | 57630 |
| rs376943048 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149430 | AGCATTCAGAAGATA[C/T]GAAAACCTACACCAT | 57630 |
| rs376984217 | in-del | -/A | 0.123105 | 0.215401 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204904 | TGTTTCTGACATTTG[-/A]AAAAAAAAATTCTAA | 57630 |
| rs377009937 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212057 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 57630 |
| rs377058890 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | SH3RF1 | GRCh38.p7 | 4:169117594 | AAGACCTTAGCCTGA[A/G]GACTTGTCTGGATGT | 57630 |
| rs377074300 | snp | A/G | 0.000262699 | 0.0114578 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116566 | TGCAGGGCTGAGGCC[A/G]GCGGCATTCTGTACC | 57630 |
| rs377083025 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142289 | TTATGTAAAGTGCTC[C/T]TTAACTTATATGTAT | 57630 |
| rs377087592 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124240 | TGGCATGTGCTCAAA[C/T]AGAAATTAAAATCAT | 57630 |
| rs377122189 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267909 | GCCAATAATTTAGAA[C/T]TCCTTCTTCTTACAA | 57630 |
| rs377182452 | snp | C/G/T | 0.00117792 | 0.0242399 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122054 | CTGAGGTTTGGACTT[C/G/T]GTTTAAATGAACACA | 57630 |
| rs377204167 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180973 | GCAACCCTTTCTTTT[A/C]TCTTTACTCACAAAT | 57630 |
| rs377206082 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241582 | CCTGAACTCCACCAG[A/T]GGAGACAGTGAGAAA | 57630 |
| rs377206755 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176157 | CAGAACTGTGAGAAA[C/T]AAATCTCTGTTGTTT | 57630 |
| rs377210129 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142599 | ATGACTCAGCAGTTG[C/T]CCTATCATCATTTAA | 57630 |
| rs377229920 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261604 | AAGTGAGACCATCTC[-/A]AAAAAAAAAAAAAAG | 57630 |
| rs377264772 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268540 | CAGAACAAAAGCTGG[C/T]TTAGATTTCATTCAC | 57630 |
| rs377269024 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165679 | GTGAAATTCAATTGC[C/T]TATTTTTAGTTTTGT | 57630 |
| rs377269945 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242726 | GAAGGGAGTGGGTTT[C/G]TTATAAAAGCGCGTT | 57630 |
| rs377272320 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094284 | CATCAAATTTTAATC[C/T]TGAAACCTTTTATCC | 57630 |
| rs377302343 | snp | C/G | 0.000153988 | 0.00877328 | missense | SH3RF1 | GRCh38.p7 | 4:169268828 | TACTTACCCTCACTG[C/G]GGGGCTCCAGGATTG | 57630 |
| rs377318199 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207530 | AGTCATATACCAAAA[A/C]CTTTTAGGATTACAC | 57630 |
| rs377325960 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170513 | ATATATTAAAACATA[C/T]GCTTTTTGAAAATTG | 57630 |
| rs377330912 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136719 | TCCAAAATTTAAAGT[C/T]ACTACTTTAAAGTTT | 57630 |
| rs377335053 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117007 | CCTTTTCTTATGAAT[C/T]ATTTTCCTTTTTTCT | 57630 |
| rs377370836 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212047 | TTCTAATTTTTTTTT[-/C]TTTTCTTTTCTTTTT | 57630 |
| rs377374133 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147431 | ATCAGTGAACAAGTA[C/T]TTCCCCTACCCTGGA | 57630 |
| rs377387494 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270328 | GGGGCCAGGTGTCGG[C/T]GGCACCCGGCAGGAG | 57630 |
| rs377411811 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151206 | AACCGGCCCTTGGGA[G/T]TTTGAATTCTAATGG | 57630 |
| rs377451671 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264331 | TATAAGAACACTGGT[C/T]TTACTGGATTAGGGC | 57630 |
| rs377466251 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155131 | AATAAACAAATAAAC[C/T]TTTCTCCATCTTACT | 57630 |
| rs377614072 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142257 | GATTGCGCCTGGCCA[C/T]AAATACTCTTTTTAT | 57630 |
| rs377618727 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139110 | GTATGCAACACCACA[C/T]CCAGCTAATTTTAGT | 57630 |
| rs377632144 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099459 | AGGATCCAGATGACA[C/T]TTCTCAAGTCTAATG | 57630 |
| rs377638572 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157319 | TCCCCAAGTTTATAA[A/T]CTGTAAGTGTATAGA | 57630 |
| rs377642199 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157925 | TTTGTATTTTTACAA[A/G]ATGGGGTCTCGCCAT | 57630 |
| rs377645435 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234143 | GGATCTCCACTGGGG[A/G]CAATTTTGCTCATCC | 57630 |
| rs377646513 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253709 | GATCTGCATCAAAAG[A/C]AGCCATTATACATGT | 57630 |
| rs377698201 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110016 | TACCCTGTAGCAAAA[A/C]AAAACAATACAAAAA | 57630 |
| rs377709837 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135932 | CAAGCAACTACAAAC[A/G]TCACGAGTTTGGACC | 57630 |
| rs377729008 | snp | A/T | 1.65094e-05 | 0.00287305 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117512 | ATGTTCTGGCCTGGG[A/T]TCCTCCTTACCTGTC | 57630 |
| rs386681930 | multinucleotide-polymorphism | AC/GT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097215 | TGTCTCTGTGTCCCT[AC/GT]GTCCCTTACACTGGT | 57630 |
| rs386681931 | multinucleotide-polymorphism | CGC/GGG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141799 | AGTGCCACCATGGCC[CGC/GGG]CTAATTTTTGCTTTT | 57630 |
| rs386681932 | in-del | AGTAGAG/CAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157922 | ATTTTTGTATTTTTA[AGTAGAG/CAAA]ATGGGGTCTCGCCAT | 57630 |
| rs386681933 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165711 | CAGTGTTTACATTAA[CA/TG]CCTTGGAGAGAGGAT | 57630 |
| rs386681935 | in-del | ACTGTACTG/GGTACTCTAAAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219982 | TACAAACTAGCGTGT[ACTGTACTG/GGTACTCTAAAT]TACAGGAAAGACAGA | 57630 |
| rs386681936 | multinucleotide-polymorphism | GAC/TAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228517 | GAGTTCCTCATCACA[GAC/TAA]CATCACTCGGACCTT | 57630 |
| rs386681937 | multinucleotide-polymorphism | CT/TG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229939 | GGCCAGGCGAGGTGG[CT/TG]CATGCCTGTAATCCC | 57630 |
| rs386681938 | multinucleotide-polymorphism | CA/TG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235829 | GGGATTACAGGTGTG[CA/TG]CCACCAGGACTGGCT | 57630 |
| rs386681939 | multinucleotide-polymorphism | AAGTCATGTTTATA/CAGTCATGTTTATG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249791 | TGAGGCATATGACTG[AAGTCATGTTTATA/CAGTCATGTTTATG]AGTGACTTATAAAGA | 57630 |
| rs397688829 | in-del | -/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094744 | AAGTATTTTTTTTTT[-/T]AAATTCAACACACAG | 57630 |
| rs397699365 | in-del | -/AAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166522 | GTTGAAAAGAAAAAG[-/AAG]NNGAGAAAGTTCTTG | 57630 |
| rs397704026 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228396 | CGCTGTGTTTTTTTT[-/T]CTGGAGGTTCTAGGG | 57630 |
| rs397708976 | in-del | -/AT | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174016 | TATATATATATATAT[-/AT]GGTGACTGAATTCAT | 57630 |
| rs397711863 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148027 | TTTTTCTCATAAAAA[-/A]GGCAACCTCAGATAT | 57630 |
| rs397719966 | in-del | -/A | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191315 | AAAAAAAAAAAAAAA[-/A]CCTTAGGAATATACC | 57630 |
| rs397725281 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142941 | TGACCTAAATATAAA[-/A]AGCAAGCTCAAACTT | 57630 |
| rs397727258 | in-del | -/A | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094508 | ACAGAGGTACTTCAA[-/A]TCACATAGCTTAAAA | 57630 |
| rs397732224 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142942 | GACCTAAATATAAAA[-/A]GCAAGCTCAAACTTC | 57630 |
| rs397736133 | in-del | -/A | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204302 | AACTAATTCAATGAA[-/A]TTTCCAGCACCTCAT | 57630 |
| rs397747567 | in-del | -/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244423 | CAGTATTTTTTTTTT[-/T]AAGCCACTGCACAGA | 57630 |
| rs397756293 | in-del | -/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106017 | TTGCAATTTTTTTTT[-/T]AGCTCATCAGCTATA | 57630 |
| rs397762159 | in-del | -/CA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269370 | TAGGGAAAAAGTTCA[-/CA]AAGGAGCCAAGAATC | 57630 |
| rs397788731 | in-del | -/A | 0.375 | 0.216506 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141277 | TTTAATACAAATAAA[-/A]CCAAGCAATCCATTC | 57630 |
| rs397799613 | in-del | -/AA | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110039 | TACAAAAAAAAAAAA[-/AA]CCACCTGGGAGGAGG | 57630 |
| rs397813461 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228395 | GCGCTGTGTTTTTTT[-/T]TCTGGAGGTTCTAGG | 57630 |
| rs397822751 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130255 | CATTAAAAAAAAAAA[-/A]TCTGTACTTTCTGTT | 57630 |
| rs397878328 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181280 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 57630 |
| rs397878990 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123905 | TCAAAAAAAAAAAAA[-/A]TTGTTATAGCTCTGG | 57630 |
| rs397880053 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208163 | GTTTTTTTTTTTTTT[-/T]CCTAAAAGGAAACCA | 57630 |
| rs397944233 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262686 | AATAAATAAATAAAA[-/A]TGATAACACTTGACC | 57630 |
| rs397996199 | in-del | -/C | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217015 | AAAAAAAAAAAAAAC[-/C]AGCCAGGTGTGGTGG | 57630 |
| rs397996200 | in-del | -/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224335 | ATTTTTTTTTTTTTT[-/T]GAAATGGAGTCTTGC | 57630 |
| rs397996201 | in-del | -/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227610 | GCTGGGATCCCTGGG[-/G]TGTTCCATAACATCT | 57630 |
| rs398083741 | in-del | -/A | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094507 | AACAGAGGTACTTCA[-/A]ATCACATAGCTTAAA | 57630 |
| rs398083742 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141276 | TTTTAATACAAATAA[-/A]ACCAAGCAATCCATT | 57630 |
| rs398092991 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211674 | TTTTTCATAATTAAA[-/A]GGGGGGAAGTGTTAT | 57630 |
| rs527237372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191801 | GGGGGAGAAAAGCCT[G/T]TTTCAACAAATGGTG | 57630 |
| rs527240647 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141358 | ATAGGCTGATAGCAT[C/G]GTATTCCATTTTATA | 57630 |
| rs527270710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242267 | AAAACTGCTTTCACT[C/T]GAAAACTTTTCTCCC | 57630 |
| rs527294421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191249 | CTATATACCAACAGC[A/G]ACCCAGCTGATAATC | 57630 |
| rs527322344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241479 | TTAATCCATCATCCA[C/T]GGAAGTAAAGGCCTT | 57630 |
| rs527323343 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134055 | TGTGGCCTGGGGTGC[C/T]CTCCAATGTACACAG | 57630 |
| rs527361521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197812 | TGAAATTTCTTCAGC[A/G]CTTTTTGGTTAGAAT | 57630 |
| rs527363542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205116 | GGAAATAGCTTCATT[A/G]AATGAACTATTTATG | 57630 |
| rs527378536 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166150 | AAGAAAATAAAAATG[C/G/T]AAACCACAGATTGGG | 57630 |
| rs527386520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256318 | GAAGGAGGAAGGAAG[A/G]GAGGGAGAAATAGAG | 57630 |
| rs527391772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127410 | GTACTCACAGTCTTC[A/G]GAACCAATTCAAATT | 57630 |
| rs527425425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204612 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 57630 |
| rs527436269 | snp | C/T | 0.35445 | 0.227135 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273056 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 57630 |
| rs527446572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177185 | TTACAAAGCAAATAA[C/G]GGATGGTATGGCATC | 57630 |
| rs527450382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169166 | TGTGAAGTTTATATA[C/G]TAAGGATTAAACAAT | 57630 |
| rs527481667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154497 | ACATGCTTAAGATCC[A/G]TGCTTTGATATTTTA | 57630 |
| rs527496749 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142664 | GCCATGTTTTAAATG[G/T]AGCACTTCAACATTC | 57630 |
| rs527496825 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272061 | TTTTGTCACTGATCT[A/G]AAGTTGACATTACTA | 57630 |
| rs527507139 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185318 | CAGTGATAGCCTGCC[C/G]CTACAAGCCTCACAC | 57630 |
| rs527512052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176280 | GGATCTGTCATGTGC[C/T]CCCCAAGCTCTGGGA | 57630 |
| rs527532848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147792 | TTTATATGCCACACA[G/T]GCACACACATGCTGG | 57630 |
| rs527533610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228515 | TTGAGTTCCTCATCA[C/T]ATAACATCACTCGGA | 57630 |
| rs527566181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104570 | TTTTAGGGGGTTAGA[A/C]CTATAGAAAATTATT | 57630 |
| rs527593742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141267 | TTTATTGATTTTTAA[C/T]ACAAATAAAACCAAG | 57630 |
| rs527595717 | snp | C/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148334 | ATTTGTCTACAAAAT[C/G]GTAAAAATAATTAAA | 57630 |
| rs527619436 | in-del | -/T | 0.165527 | 0.235296 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146233 | GTTTTATATATATAC[-/T]TTTTTTTTTTTTTTG | 57630 |
| rs527643501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105605 | CAGGAAGAAGAAGAG[A/G]GTTCTTCGCTAGACA | 57630 |
| rs527653086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257951 | ATTAAAGGCAGATTA[C/T]TGGTGTCAATGGGCA | 57630 |
| rs527664039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163477 | TTGCTTAGTAAATAC[C/G]TATATTTAGGAGGCA | 57630 |
| rs527671700 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157024 | CTCATAAAAAACAAG[A/C]TTAACTTCCTACATT | 57630 |
| rs527699082 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164529 | TGGGCACTTGATTCT[C/G]AGACATGGGAGGTAC | 57630 |
| rs527710054 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257291 | AAAAGTTCTGTACTC[C/G/T]CTGGCATCTCCCCTA | 57630 |
| rs527712936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265504 | TTGAGATGGAGTTTC[A/G]CTCTTTTTGGCCAGA | 57630 |
| rs527725827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162992 | CCACCATCGCTAATG[C/G]AGTGTCTAACTCAGC | 57630 |
| rs527726664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149954 | CTATGTACCTACACT[A/T]CTACTTCTTATTCTT | 57630 |
| rs527755686 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139971 | CTATTTGATTTCTAT[C/T]CCTCTAAATAGCCTA | 57630 |
| rs527767634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099523 | TGTAGTTGCCATGTG[A/G]GGCAAGTTAAACATT | 57630 |
| rs527776366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264967 | ATTAATATCATTTCA[C/T]CCTTAAGATCTCAGC | 57630 |
| rs527788839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169610 | TCAAAAAATAAAAAA[A/T]AATAAAAAAATAAAA | 57630 |
| rs527793270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143230 | TTTTAAAAGACAGAA[A/G]GAAATAGGTAAAACT | 57630 |
| rs527794570 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125491 | GGAAGTAGTCCAGTA[C/T]GTCTCAAACTTGGGC | 57630 |
| rs527817926 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106070 | ATGTAATGTAAAATA[-/T]TTTTTAACAGTATAT | 57630 |
| rs527836812 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186581 | ACCAATGTTAGCAAT[A/G]AAATTTCTACAGATA | 57630 |
| rs527837971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119973 | TTTACATAAAATATA[C/T]AAAATTTTGCATATC | 57630 |
| rs527838565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193612 | CTAAGGATGCTACGG[C/T]TTATTGTAATGGCTG | 57630 |
| rs527895889 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204550 | CATATATTACCTTCT[-/C]TTTTTTTTTTTTTTT | 57630 |
| rs527902373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192938 | ATATATATATATGAT[A/G]GAATACTACTCAGCC | 57630 |
| rs527981791 | in-del | -/TATAGAA | 0.0444908 | 0.142359 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218391 | ATAGAATATATATAT[-/TATAGAA]TATAGAATATAGAAT | 57630 |
| rs528025176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207433 | CCCTGTCTCAAATAA[A/G]TAAGTAATTTTAAAG | 57630 |
| rs528041900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108785 | ACTGCCTGCATAAGT[A/G]CAGTGGCAGTGCTGT | 57630 |
| rs528044055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253684 | CTCTGGAATTACTTA[G/T]TATACAGATGATCTG | 57630 |
| rs528045671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261415 | AAAAGCAACATGAGG[C/T]CCCAGGGAAAATGTT | 57630 |
| rs528051452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166327 | GGAACCCGAAGCCAC[A/G]AAGGCTGATGCTGGT | 57630 |
| rs528062568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160031 | GCTAATGTAAGGCAT[C/T]GGAAGCCTGCATGAA | 57630 |
| rs528071299 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234798 | TTCTAAGTCGGGGTT[-/TC]TCAGTCTTGGCACTA | 57630 |
| rs528106064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260832 | ACATAACTGAGTTCA[A/T]GTCTGTATTTTATGT | 57630 |
| rs528111082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101919 | AAAGAAGCTCCACAG[A/G]CTTCCAATGCTATGG | 57630 |
| rs528126581 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152740 | GAAACTCTATCTCAA[A/C]AAATAAAAAAGGAGA | 57630 |
| rs528131175 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268072 | AATACAGATTATTTA[C/T]ATATATTTCTAATAA | 57630 |
| rs528153723 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217964 | TATGGTTTTCCAAAT[A/C]ATCACAACACAAATA | 57630 |
| rs528162623 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237339 | TTTATTTACCTGGGG[A/G]ACAATTAAAGCTGAT | 57630 |
| rs528183238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268438 | ATACTTACAACATAT[A/T]TACTACATATGTACT | 57630 |
| rs528186198 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214964 | TTCTTTTCTTTGTCT[C/T]ATAACATTAGCTAGG | 57630 |
| rs528207557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224945 | GAGTCTCATTCTGTA[A/G]CAGGGTGCCCAAGGG | 57630 |
| rs528239590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123248 | CTTATTTCTGTTTTT[C/T]GGAATAAAAATTTGA | 57630 |
| rs528240473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189680 | TTGGGACCAGGCAGG[C/T]GTGGGCTCCTATTTC | 57630 |
| rs528241897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131313 | AAAGTTTGAAACTAA[C/G]TAGATCCAGGGGGTG | 57630 |
| rs528243221 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095858 | TGATTCCTACCAAAC[C/T]AGAAAGAGAGGGAAT | 57630 |
| rs528249471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197096 | CTACAACTTCCACCT[C/T]CTGGGTTCAAGCAAT | 57630 |
| rs528258231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248404 | AGAAAACCAAACACT[A/G]CATGTTCTCACTCAT | 57630 |
| rs528274019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240358 | CAAACCACCATGCCC[A/G]CCTGATTTTTTTAAT | 57630 |
| rs528277433 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212495 | AAGCAAGTATCTATA[A/T]GTTTTTTCCCTTTTC | 57630 |
| rs528285149 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180158 | ACAAATGCAGCAAAA[C/T]GCAACCCAGGCTTTA | 57630 |
| rs528313161 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196182 | TGTATTTTTTTCTAT[A/T]GCTATTGTTTCCCTA | 57630 |
| rs528333148 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176505 | TGAACAAAACCAATA[-/T]TTAATATTTACTAAG | 57630 |
| rs528335158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247707 | CATCATGACATTCCT[A/G]CACACGACAGAAACT | 57630 |
| rs528344807 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210743 | GCCAATTAAAGGCTG[C/T]TCCAATATCATATTC | 57630 |
| rs528361329 | snp | C/T | 0.000240329 | 0.0109593 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116623 | GCGTTCCTGGTTGTG[C/T]GCTGCAACTAGTAGA | 57630 |
| rs528374580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203124 | TATTTGACCAAACGT[A/C]TCACAGAAAACACTT | 57630 |
| rs528379322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254263 | TACTACTTTTTCCAC[A/G]GTCATGAGCAGAAAA | 57630 |
| rs528411283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159365 | AATAATAGTAAAACA[C/T]AGCAATCGACAGAGA | 57630 |
| rs528422071 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268095 | TCTAATAAATACAGA[A/C]ATTTTGTGTGACAGT | 57630 |
| rs528440460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270306 | CCGCTCGCCGCAGAC[A/G]CACCCCGGGGCCAGG | 57630 |
| rs528483960 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202199 | TTAAGGGCCTACTTC[A/G]TGTTCTTGGTGCCGG | 57630 |
| rs528504129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182740 | GAGGCAAAGTGTTCA[A/T]GTGTAAAGAACGATA | 57630 |
| rs528546991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161047 | TGCTTTTCTTCTGTA[A/T]CCTCTCATCAGGCCA | 57630 |
| rs528555729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233365 | GTACAGTAGCATATA[C/T]ATCATAAAATAATTA | 57630 |
| rs528587851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118747 | CAGGTTTGAGCCAAC[A/G]CGCCTAGCTGGTGTA | 57630 |
| rs528591509 | in-del | -/TCAC | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220660 | CAATGGGATTAGCTT[-/TCAC]TGTACTGGATTCCTC | 57630 |
| rs528620231 | snp | A/G | | | stop-gained | SH3RF1 | GRCh38.p7 | 4:169116457 | GAGGGGCACTGGCTC[A/G]ACTGATACTGATGGC | 57630 |
| rs528634119 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263277 | ACAAAAAAGAACCCC[A/G]TCATAGATAGAGACT | 57630 |
| rs528655283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161635 | ATGCATTTCTTACTG[C/T]TCCATAAAGTAAAAA | 57630 |
| rs528663173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255525 | GAGGGGAAGGGTGGG[C/T]AAGGTTGGGGAAGGG | 57630 |
| rs528680163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212740 | TTTATATCAGGGTTC[C/T]CTCTTGGTGTTCTAT | 57630 |
| rs528680785 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113581 | ATGGGGAGAACTCTG[C/T]GGATGGGAGGATGAT | 57630 |
| rs528698959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168038 | CCAGCTACTCAGGAG[A/G]CTAAGGTAGAAGGAT | 57630 |
| rs528710552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263098 | GTCTTGCTTGGGTCC[A/G]GTATGAGTTAATACA | 57630 |
| rs528720726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140193 | TAAATCAGGCAGAAA[A/C]ATAAAGCAGCTTTTG | 57630 |
| rs528724207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132186 | ATTATTATCAAGGAA[C/T]CCTTGGGGCAGAAAA | 57630 |
| rs528743979 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145522 | AATATGCATGTAATA[-/C]CAATGTAATAAACCA | 57630 |
| rs528760297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175364 | AGGCTTTCTATCATC[C/T]GGTCCCGGCTAACCT | 57630 |
| rs528772164 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169270976 | CCGCGGCGGCACCGG[C/G]AGACTCCTCTCTGCT | 57630 |
| rs528773164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262484 | CCAGCCTGGCCAACA[C/T]GGTGAAAACCCACCT | 57630 |
| rs528818001 | snp | G/T | 0.145978 | 0.227331 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219993 | GTGTGGTACTCTAAA[G/T]TACAGGAAAGACAGA | 57630 |
| rs528823565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247970 | TTAGAATGGCGATCA[A/T]TAAAAAGTCTGGAAA | 57630 |
| rs528827322 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171058 | ACCTAAAGGTTTCTC[C/T]ACACATAGTGAAGTA | 57630 |
| rs528845808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254824 | CAGGGGTTGGATAGC[A/G]TCCAAAGGAGAGTGA | 57630 |
| rs528886353 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095953 | TTGTATGTTTGGTTT[C/T]CCAAAGAAGAAAACC | 57630 |
| rs528887021 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103075 | ACAGGTGCCCGCCAC[C/T]GCGCCTGGCTATTTT | 57630 |
| rs528892735 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212062 | CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 57630 |
| rs528909192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262167 | ATATAGTAAATGAAT[C/T]AGCAAATCATTGAAT | 57630 |
| rs528910125 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116043 | CTGGCAAGTAGTGGG[C/T]GTTTAAACACAGAGA | 57630 |
| rs528910149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254455 | TCCATATGATCACAA[A/G]TATGTATTAAAGCAA | 57630 |
| rs528925451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146728 | TCTTGAGAAGTTTAG[C/T]AGAAGTAAGAAAAAA | 57630 |
| rs528955001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211279 | TGAGTTCAGGAGATC[A/G]AGACCATCCTGGCTA | 57630 |
| rs528962823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140220 | TTTGCTGTAAGTATA[A/G]CAACCTTTGGTAACA | 57630 |
| rs528971677 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261542 | TGAAATAAGAATAAT[A/C]ATGTATAGTGAGCCG | 57630 |
| rs529000648 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235478 | TTTCCATTTAAATAT[A/G]AGCCAACTGAAGCAC | 57630 |
| rs529003784 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166365 | TGAAAACGGGTAACT[A/T]CAAGGCTAAAAGCCC | 57630 |
| rs529010927 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183587 | GCCCAGCCAAAACAA[-/T]TTTTTTTTTAATTAG | 57630 |
| rs529012796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116809 | CTGGATCCCCAGACA[C/T]TATCTATTGTCCTTC | 57630 |
| rs529035960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241199 | CGCGCCACTGCACTC[C/T]AGCCTGGGCGACAGA | 57630 |
| rs529042837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182853 | GAACTGCTTTCTTCC[A/C]ACCAAAAAAAAAAGG | 57630 |
| rs529063385 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122567 | TAATCTTAAGATTAA[C/T]AGCATTTTAAAGTAT | 57630 |
| rs529065851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233579 | CTCATTGATAAACAC[A/G]AATTGTCATTGTAAG | 57630 |
| rs529086987 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236758 | CTAACAATCTGAGAC[A/T]TGGATATGTAAATAC | 57630 |
| rs529096305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240819 | TACCATACTTATACC[A/G]CTTGTACATAAGCCC | 57630 |
| rs529123792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190633 | TTCACAGCAGAATTC[C/T]ACCAGACATTCAAAG | 57630 |
| rs529151828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248434 | TAAGTGGGAGTCGAA[C/T]AATGAAAACACATGG | 57630 |
| rs529158884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160117 | GCCTGTTTTTTTCCC[C/T]ACCTCAATTAGCTCT | 57630 |
| rs529184480 | in-del | -/T | 0.0360663 | 0.129354 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196903 | ACATGTTAATCTCTA[-/T]TTTTTAAGTCTGTTA | 57630 |
| rs529186694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197169 | TGCTACCATGTCTAA[G/T]TTTTGTATTTTTAGT | 57630 |
| rs529195564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110129 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCAAGG | 57630 |
| rs529223215 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203718 | CTAGAACAGTATCTG[G/T]TACACAAAAATAACT | 57630 |
| rs529225185 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160806 | TGATTAAGGATAAAC[A/G]GTTAAACGACTTGGA | 57630 |
| rs529228529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102501 | TGACTTGCTGTGTCT[C/G]CCTGAACTCTTTATA | 57630 |
| rs529232508 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118876 | TTGCACATGCTCAGG[A/G]TTACAGCCAACTCTA | 57630 |
| rs529272314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186791 | GCAGGCGGATCACGA[A/G]GTCAGGAGATCGAGA | 57630 |
| rs529285056 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271036 | CCGCCGCCGCCGCCT[C/T]CCACTTTCCCAGCCA | 57630 |
| rs529304746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175515 | CCTTCTGCTTAGAAT[A/G]TTCTTTACAGGCTTA | 57630 |
| rs529324853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227419 | TTTCACTGATAGGTA[A/C]ATGACAAAGTGATTC | 57630 |
| rs529327598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111208 | TGGGAGGCTGAGGTG[A/G]GAGGATTACTTGAAC | 57630 |
| rs529365359 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183437 | AAGCACTTGCCACCA[C/T]GCCCAGCTAATTTTT | 57630 |
| rs529370855 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259457 | TGTGTTTACAGCCAC[C/G]CATATGTCACCATTC | 57630 |
| rs529387762 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155408 | GGACTTCTTAATACT[C/G]AAATTGCATAATTAA | 57630 |
| rs529389435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112068 | ACTGCAGAGCAGCTG[A/G]GTACAGAGAAAAGGA | 57630 |
| rs529400671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145200 | GTGTCCATCAACGGT[A/C]TACTGGATAAAGAAA | 57630 |
| rs529405021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226510 | AAAAAAAAGAGCAAG[A/G]AAGATCAGAATACAT | 57630 |
| rs529416768 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140876 | TTTAATTCACAACCC[A/C]CTAGAGCAAGCTTGT | 57630 |
| rs529421020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132961 | TAAGTAATCTTTCAA[C/T]TTATGTATTTGAAAG | 57630 |
| rs529448773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104731 | AGATGGCAAAACCCC[A/G]TCTCTACTGAAAATA | 57630 |
| rs529463703 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170866 | AAGGGTTCAGAGATA[C/G]GGAAAACAGCTCTAA | 57630 |
| rs529481992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133427 | TTGCAGTGAGCCAAG[A/G]TTGTGCCACTGCACT | 57630 |
| rs529490589 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256420 | TCAACCAGTGTCACA[C/T]TATAGTCGTAAAACC | 57630 |
| rs529528383 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125776 | ACCCTACATATCAAC[A/C]TGTCTGAACAGTCCT | 57630 |
| rs529535885 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171259 | ATTTCGGTCCATGAA[A/T]CCTCTCTGACCACAC | 57630 |
| rs529548544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169012 | CTTCTACAATGTCAT[C/T]AGGAAAAGCAGAAAC | 57630 |
| rs529548897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161662 | AAAAAGATTCAGTGA[C/T]CTCCTAAAAAGAAAA | 57630 |
| rs529568080 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239412 | AGTTCTGAATCACAA[-/G]TGCTGTTCAGAAAAC | 57630 |
| rs529602247 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199616 | GCTTAGTGAATGCGC[-/A]AAAAAAAAAAAAATA | 57630 |
| rs529608813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171423 | AGATTAATGAGGGGG[A/G]AACAGACCGTATTCA | 57630 |
| rs529641822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221526 | CCAACAACTCAGTTC[C/T]GAGAAAAGTTTGAAA | 57630 |
| rs529647931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212810 | CATTACAGAACCATA[C/G]AGCATAATTTCAGTG | 57630 |
| rs529677210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123020 | TCTTTAGGGTCTGTA[C/T]ACTGAAACTCTTGGG | 57630 |
| rs529678907 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172809 | ACAAAGCAAGCGAAG[A/G]AGGTGGGATGTAATG | 57630 |
| rs529696395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216584 | GGTTGCTCACCTCTA[C/T]AGTCCGAGAACTATG | 57630 |
| rs529702851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223695 | GGGGTGATGGGCAAG[A/C]ATATCAACAAATAAT | 57630 |
| rs529734540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115167 | GAGACATTAAAAAAA[A/C]CCCCAAAAACTATGG | 57630 |
| rs529735470 | snp | A/C/T | 3.36707e-05 | 0.00410298 | missense | SH3RF1 | GRCh38.p7 | 4:169107042 | CAGGAGCCTGCCCTG[A/C/T]CATGGCCACCTCCTG | 57630 |
| rs529744474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230596 | GGGCGCAGTGACTCA[A/C]ACCTGTATTCCCATC | 57630 |
| rs529780525 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243639 | CCCCTATTAGTTTTG[C/T]TATCTATATTCTCCA | 57630 |
| rs529788510 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187052 | AAAAGAAAAGATTCT[C/T]TTTAAAACCTCAAGG | 57630 |
| rs529797068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115824 | ACACTTTTGATCAAC[A/G]GTTTCATCCCCCTCA | 57630 |
| rs529811046 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237188 | GGAATACAATAAGCA[C/G]AAGAGGAGTGATGTG | 57630 |
| rs529812314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143679 | TAGGACAGGGAGGAA[C/G]ACGGACTCCTAATAC | 57630 |
| rs529817193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158534 | GTAATGGTAAGTCAT[C/T]TCCATGTTTAATGCA | 57630 |
| rs529824239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135929 | ATACAAGCAACTACA[A/G]ACGTCACGAGTTTGG | 57630 |
| rs529857125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126709 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 57630 |
| rs529859465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107771 | GTGATCAGAGTTAAG[A/G]GCTAAACCACTTCTC | 57630 |
| rs529874625 | snp | C/T | 6.96015e-05 | 0.00589881 | missense | SH3RF1 | GRCh38.p7 | 4:169136587 | GCACAGGAGGCTTAT[C/T]CCATTCTATCAGCTG | 57630 |
| rs529880288 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129345 | AGTCTTTCTCTACTA[A/C]CGAAGGTTGCATTTG | 57630 |
| rs529921361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208196 | TTCCTTCACTAACCC[G/T]CCTTCATCCCCACCC | 57630 |
| rs529942217 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164277 | TGAATAAATTAATGA[A/C]AGAACAAAAGTTATC | 57630 |
| rs529965639 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272008 | TCCATAGGTTTTGAG[A/G]TTTTTCAGTCTCGAT | 57630 |
| rs529989849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188489 | CCGAAAGGCCCTGTA[C/T]ACAGCTTGTTACTCT | 57630 |
| rs530041856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224380 | TGGAGTGCAATGGTG[C/T]GATCTTGGCTCACTG | 57630 |
| rs530050678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195082 | TAAATAACATACTTT[A/C]ACATTTCCTTTAGCT | 57630 |
| rs530058996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187858 | GCCTTATTAGAAATA[A/G]GGTCTAGGGTCTTCG | 57630 |
| rs530081870 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238226 | TTAACATATCCAAGC[A/T]TGGTCAGAATTAGGG | 57630 |
| rs530090865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138366 | GAAAAGCTACTTCAT[C/T]TCCTCCATCCCAAAC | 57630 |
| rs530124223 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137596 | TGATTTTTCCATCTC[A/G]GCATTACACATTGGG | 57630 |
| rs530155162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246708 | AAATCAAATTACCAA[A/G]GAGCAAATTTAATTT | 57630 |
| rs530181841 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100825 | ACAAAAGTCCCAAAC[A/G]CTCCCCTAAGCCTGA | 57630 |
| rs530229363 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218268 | TTTATATATAATATA[G/T]AATATAAATATATAA | 57630 |
| rs530255441 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210038 | TGAGCTCAAGCAATA[C/T]GCCTGTCTTGGCCTC | 57630 |
| rs530258198 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175825 | TGTATCTTCCCTCTC[C/T]CCCCATCCCCCAATT | 57630 |
| rs530268425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269612 | AAGGAACATAATTTC[C/T]TAAGCTCTGAAAGTG | 57630 |
| rs530281039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232261 | GAATGATGTTCAAAT[C/T]CACATTTGGGAAAGA | 57630 |
| rs530283437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224995 | TAATCCAACAGCAGT[C/T]GGGAAAGAAGAGAGA | 57630 |
| rs530310532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101757 | TGTTCCCTTTGAACA[A/C]AGCGCTGTGGAGGCA | 57630 |
| rs530397728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268390 | AACATAAAAATTAAG[A/G]CTTGATTTCCTATTT | 57630 |
| rs530398041 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174828 | AAAGCTCCTTAGTGA[-/CT]CTCATATGAAGCGCT | 57630 |
| rs530399523 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260133 | AGAGCTGGGGGCTCG[C/T]GGAATGCTGAGAAAA | 57630 |
| rs530413217 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123166 | TTAAGTGTAAATGGC[G/T]TCTATATGTCAGCAT | 57630 |
| rs530416069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158599 | AGTCTGGCAGTAGTG[C/T]GGAAAATGGACGTGA | 57630 |
| rs530425763 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211048 | TCACTTCCTCAAAAC[-/AT]ATTTATTTTTATAGA | 57630 |
| rs530456637 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121348 | TTCAAATGGCACTTG[G/T]TAGGCTTGAGAAGTA | 57630 |
| rs530459299 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267634 | CTGTTTTCTGATCAG[G/T]TTTTCCAGTGATTAA | 57630 |
| rs530488399 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187981 | ACATCAGAGTGAAGA[A/C]GGCTGGGTGGTGAGA | 57630 |
| rs530497651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165068 | CAGAGAGCAGGAATA[C/T]TTACTGGGAAGATTC | 57630 |
| rs530532032 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240970 | GCGTGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 57630 |
| rs530536097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152239 | AGGTCTGAAAGAATC[G/T]CCGGAGGGGAAGGGT | 57630 |
| rs530545581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107793 | CCACTTCTCACATGT[C/T]GCCACCTTGATTAAA | 57630 |
| rs530571616 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123688 | CGAGGTCAGGAGATC[A/G]AGACCATTTTGGCTA | 57630 |
| rs530583552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224394 | GCGATCTTGGCTCAC[C/T]GCAACCTCCACCTCC | 57630 |
| rs530597173 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101345 | ACGTTATGCTAAGTG[A/G]AATAAGCTGCATGCA | 57630 |
| rs530645664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122374 | TAAATCCATAGAACA[A/G]GACTTTAATGGAATC | 57630 |
| rs530647129 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231301 | AGTTGGGTGTGGTGG[C/T]TCATGCCTGTAATCC | 57630 |
| rs530652662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130502 | CCTGGTGCTCAACTA[C/G]CCTCCTAACAATTTC | 57630 |
| rs530662242 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101900 | AAACAGAGTCTTGCA[A/C]TATAAAGAAGCTCCA | 57630 |
| rs530692135 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182321 | ACACTCACAAAGGAG[C/G]GTGACCCAAAAATCA | 57630 |
| rs530714366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246918 | CTTGAATAATCTCAT[A/G]GCTCTTCATCTAAAA | 57630 |
| rs530723609 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260683 | TCTCTCCTTCAGTCA[A/C/T]GCAAAAGAGAAATAT | 57630 |
| rs530741951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202353 | TCTCAGCCCTCTCTA[C/T]TTTTCTCTTGTGCCC | 57630 |
| rs530783230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253507 | AAGGATCCCTTGGGA[C/T]TAATTTATTCTAACT | 57630 |
| rs530794289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209986 | TTTTTTTGTAGAGAT[A/G]GGGTTCGCCATGTTG | 57630 |
| rs530831523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123216 | AATGATTTCTAAACA[A/G]AGCTTATACCAGTCA | 57630 |
| rs530835165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180990 | CTTTACTCACAAATT[C/T]GCTCTAGGGACCAGA | 57630 |
| rs530837092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189562 | CTTTCAAATCATAAA[G/T]TTTCTGTTGCCACGG | 57630 |
| rs530859062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209277 | CTGAGTGACAGAACA[A/T]GACCCTGTCCGAAAA | 57630 |
| rs530875989 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231444 | CATGGCGCATGGCTG[C/T]AATCCCAGCTACTCA | 57630 |
| rs530886905 | in-del | -/A/AAAAAA/AAAAAAA | 0.201727 | 0.245295 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197624 | GCAAGACTCTGTCTC[-/A/AAAAAA/AAAAAAA]AAAAAAAAAAAAAAA | 57630 |
| rs530892036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132104 | CATTCTTTCCTTGCT[C/T]TGTGTGTTTTGTCCA | 57630 |
| rs530892447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196129 | GAACACAATAATTAT[A/G]AAGTCTATTTCTATA | 57630 |
| rs530897484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188579 | CCCTTATTTACAGTA[C/T]AAAAGCTAATGAAAA | 57630 |
| rs530931223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247614 | ATAGGAGTACAACTA[C/T]ATGGGCCAGAGAGAA | 57630 |
| rs530947249 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259524 | GGCAGACATATACGC[A/G]ACAAAAGGATTGCAG | 57630 |
| rs530985363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231865 | ACATTCAAGGATATA[C/T]AAGTATCAGGTCCTG | 57630 |
| rs530990602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152670 | TGAACCCGGAAGGCA[A/G]AGGTTGTAGTGAGCC | 57630 |
| rs530996386 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220666 | GATTAGCTTTCACTG[-/T]ACTGGATTCCTCTGT | 57630 |
| rs531015917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125526 | GGCTACAGGCCAGCT[C/T]GCCAGTAAAGTGCTT | 57630 |
| rs531021693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117418 | TGCCTAATGTTGTTC[A/G]TTATTAAAATTACAT | 57630 |
| rs531029127 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186142 | TTAGTGCAAGTAAAG[A/G]AATGATAACTTCTCC | 57630 |
| rs531046439 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239271 | TATTTTTGTAACCAT[C/T]GCATATCTCTATTAA | 57630 |
| rs531047169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174804 | GGGTCAGAAGCATAC[A/G]GATTTTGAAAAGCTC | 57630 |
| rs531053149 | snp | A/G | 0.237882 | 0.249706 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145837 | TTCTATATAAAATAT[A/G]TATTCTATATATTAT | 57630 |
| rs531066714 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202529 | TATAATGAATAAAAA[C/T]CTTCAGCTTACAGCT | 57630 |
| rs531074699 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233753 | TCCCTCTACCCTATT[A/G]TTTCACAGAACCATT | 57630 |
| rs531081661 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226315 | TTCACAGTCACTTGA[C/G]ATTTATAATTCAGTT | 57630 |
| rs531109402 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209549 | GGACCATATCTTGCT[G/T]GTAATTGCAGTATTT | 57630 |
| rs531115228 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145197 | TGAGTGTCCATCAAC[C/G]GTCTACTGGATAAAG | 57630 |
| rs531115797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139187 | GCTCAAGCGATCCTC[C/T]TGTCTCAGCCTTTCA | 57630 |
| rs531129377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102392 | ATCAAAGATCATACA[C/T]AGATTTTTTTTTTTC | 57630 |
| rs531134942 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095183 | CTCCACAGTCACAGG[A/C]GTAGTCTCCTGGTTA | 57630 |
| rs531159748 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119222 | GATTATCCTGCCTCA[A/C]CCTCCAAAGTAGCTG | 57630 |
| rs531163266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261568 | AGCCGTAAACACTCC[A/G]ACTGCACTCCAACCT | 57630 |
| rs531163323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270228 | GGGGGAGCCCCAGGG[C/T]TGCACCCCCGCTCCC | 57630 |
| rs531166524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185369 | AGCAAGGAAAAGGGA[A/C]GAATTCTAAAATTTT | 57630 |
| rs531170632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166469 | ATATATTCCAGAAGT[G/T]CCATGTACAAGAGGA | 57630 |
| rs531204570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219127 | CACAAAAAAATTACA[A/G]TGAGGAGCTGATAGA | 57630 |
| rs531225346 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184864 | AAAACAGACAGCAGT[C/G]GGCAAGATTACACTT | 57630 |
| rs531229649 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192356 | TCGCAAAAGAAGATA[C/T]ACAAATGGCCAACAA | 57630 |
| rs531232984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131494 | TTTTCTATTTTTCCT[A/G]TGAACCAAAGTCTAT | 57630 |
| rs531279672 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105510 | ACAGGGCTTATTACT[C/T]TGAGTGTAACTGAAT | 57630 |
| rs531292450 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191896 | CAAATCAACTCAAGA[C/T]GGATTAAGGACTTAA | 57630 |
| rs531299625 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146162 | TCTATATAAAATATT[-/A]TATATCTATATATTA | 57630 |
| rs531345186 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222703 | TCAGTTTATTGCTTC[C/T]CTTGTTAATCTTTCA | 57630 |
| rs531347992 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163562 | AACCACAGTAACAAG[G/T]ATAATTCCTGAAACA | 57630 |
| rs531389846 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205582 | TCCTTCTTGGGTTCT[C/T]TTTTCCCATTTGCTC | 57630 |
| rs531409990 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097989 | AAAGTGATGTGAATA[A/T]GCCATCTTAGAAGGG | 57630 |
| rs531437433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242367 | TTTAAAATGAAATAT[C/T]GCTTCTAAAATTATC | 57630 |
| rs531439851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169681 | GAGAAGGAAGGAAGA[A/T]CTTTGGACCACTTAA | 57630 |
| rs531456624 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120697 | GTAGACATGGATTTT[C/T]AAAACCTTGGCTATG | 57630 |
| rs531472282 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189100 | ATTCTGAAGAGATTC[C/T]TGTCAGTTCAAGTAG | 57630 |
| rs531483218 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243337 | GGCCAACATGGAGAA[A/C]CCTCGTCTCTACTAA | 57630 |
| rs531497117 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138617 | GAGGCAAAAAATATG[A/G]ATAGAGGAAACTATC | 57630 |
| rs531502396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170434 | TTTAAGATGAGAAAA[C/T]TAATAATCGGAATAC | 57630 |
| rs531504834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163062 | AGCCTTGCTGTTTTG[C/T]GGGGGGCATTAATGG | 57630 |
| rs531508954 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265550 | GCGATCTCAGCTCAC[A/T]GTAAACTCTGCCTCC | 57630 |
| rs531524749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223124 | CTGGACCTTCCTGGG[G/T]CCTTTCTGCCAGGAA | 57630 |
| rs531543072 | snp | C/T | 0.00914312 | 0.0669923 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095125 | TGGATCCTGCCACAA[C/T]TGTAAGGTGTGGGCA | 57630 |
| rs531567876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178398 | GGCACAGAATCACAG[C/G]GATTTGGGGCTAAAA | 57630 |
| rs531578507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148728 | AGAGGGGGTTTTTTT[C/T]GGTTCTGTTTCATAG | 57630 |
| rs531585684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143291 | TGTATCTACACTATG[A/G]TCACTTCAACATGTA | 57630 |
| rs531599836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100278 | AAAATCTGCATCCCA[A/T]CCACTCCTCTTCATT | 57630 |
| rs531600912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098596 | CAAGATCTGAAGCAA[A/C]AGCACAGCACAGAAG | 57630 |
| rs531604223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207985 | GGTCCTGGGATGAGG[C/G]GGATGGGAACCAAAA | 57630 |
| rs531635715 | snp | A/C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273079 | TTTTTTTTTTGAGAC[A/C/G]GAGTTTCACTCTTAT | 57630 |
| rs531646114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142285 | TATATTATGTAAAGT[C/G]CTCTTTAACTTATAT | 57630 |
| rs531711026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150765 | TGGAAACTGTGAGGA[A/G]TCCTGAAACCAACGC | 57630 |
| rs531713496 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141398 | CCATTTACTATGTCT[A/T]GGCAGGCTCGTACAA | 57630 |
| rs531722093 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258013 | CAAGATCATATCCAG[A/G]TGCCAATCTGAGTTT | 57630 |
| rs531742441 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094161 | GTATGCAAAGAATTT[C/T]TGTGAGGTACAAATT | 57630 |
| rs531772994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143719 | TACATCCTGCCAAGG[A/G]AAAAGGATTTTCAAA | 57630 |
| rs531791804 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125848 | GGAATGGTTCAAGCT[A/G]CTACATGGAGATGCC | 57630 |
| rs531820269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126220 | ATAACAGATCCTCAA[C/T]GAGCATTTCATGAAT | 57630 |
| rs531884099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164345 | TGGAAAAAGAACACA[C/T]CTAAAGGAAAAGCAA | 57630 |
| rs531895752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121842 | ATGAAAATAAAGATA[A/G]AAAGTTCAAACAGGA | 57630 |
| rs531898175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187615 | TTTTCACTAGAATAA[C/T]CTCCAATAACAACAA | 57630 |
| rs531902465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179476 | AAGAGAAAACTAATA[C/T]AACCATATGAACCAA | 57630 |
| rs531928688 | snp | A/C/T | 3.40259e-05 | 0.00412456 | missense | SH3RF1 | GRCh38.p7 | 4:169106920 | GGCGAGGAGGTGGAG[A/C/T]GATGGGAACTGCGGA | 57630 |
| rs531939609 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220648 | GGCACCCAGCTCCAA[C/T]GGGATTAGCTTTCAC | 57630 |
| rs531951395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099699 | TTGAAGTGAATTAGA[C/T]TAATATATGCATTTT | 57630 |
| rs531966894 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187114 | TAACTCTTAAATTAT[G/T]AGAGCAACCTGCAAC | 57630 |
| rs531995434 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248503 | GGGGTGGGAGGCAAG[A/G]AAAGGGAGAACATTA | 57630 |
| rs532020959 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120993 | ATAGCAACATACCTA[A/G]AATAGAAAATAATAT | 57630 |
| rs532033835 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226490 | GAGCCTGATTTAAAG[-/A]AAAAAAAAAAAAGAG | 57630 |
| rs532068862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185457 | CAAACAAACAAAAAA[A/C]CCACAAAACATTACT | 57630 |
| rs532114237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129138 | AACAGCACAACTTAC[A/G]ACTGTGGGCAGGCAG | 57630 |
| rs532122887 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244964 | TTATTTATACAGATC[A/C]CCTGACATACAGAAG | 57630 |
| rs532139653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248260 | CCATTAATGATAGAC[C/T]GCATAAAGAAAATGT | 57630 |
| rs532143171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229934 | TGCTTGGCCAGGCGA[A/G]GTGGCTCATGCCTGT | 57630 |
| rs532171622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121866 | AACAGGAGTTGTACA[A/G]AAGAGGCAGTTTCAT | 57630 |
| rs532207417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236410 | GCCAATCCACACAAC[A/G]TATACCTTGAGTGAG | 57630 |
| rs532207498 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148541 | CTTTCCAAACGTTCT[A/G]GAACATGATTATATT | 57630 |
| rs532234015 | snp | A/C/G | 0.000291909 | 0.0120778 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122192 | AGCAGCAGCAGCGGC[A/C/G]GTGGCGCCTGGTGGT | 57630 |
| rs532244607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163621 | ACAATCTGGAGACAG[C/T]TCCCAATTACCTCTT | 57630 |
| rs532244820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134802 | CATCCAACAAATACA[A/T]GTTGAGTGCTTTCTG | 57630 |
| rs532281502 | in-del | -/AC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217013 | AAAAAAAAAAAAAAA[-/AC]CAGCCAGGTGTGGTG | 57630 |
| rs532287450 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268610 | ACAGAGACTATCTAG[A/G]GATAATTTTCAAAAC | 57630 |
| rs532290801 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163278 | TTCCAAATTTCAAAA[A/C/T]GAAAAAATGCTATTA | 57630 |
| rs532294621 | in-del | -/TAA | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106035 | CTCATCAGCTATAAT[-/TAA]TGTTAGTGTGTATAT | 57630 |
| rs532304946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170584 | TGTTCACCAGGCTGT[A/G]AGCTATGTGAGGGCA | 57630 |
| rs532317310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259188 | AAAAATAATAATAAT[A/G]ATAATTTCCTTAATC | 57630 |
| rs532339245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216043 | TCCTGAGCTCAAGAG[A/G]TCTGCCCACCTTGGC | 57630 |
| rs532359130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099474 | TTTCTCAAGTCTAAT[A/G]TCAACATGCTAAAAA | 57630 |
| rs532369437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266430 | CTAAGGGAAGCGTCC[A/G]AAGAAGTGCCTTACA | 57630 |
| rs532375452 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143104 | TTGAATGAATAAAAA[C/T]GTTTGTCTCTTAGAA | 57630 |
| rs532408147 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223632 | TCTTTTTTAAAAATT[A/G]TGTCCTTCTTTCCAT | 57630 |
| rs532418537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193727 | GCCAGTCACCTGAAG[C/G]AAAGGTCCCTCAGCC | 57630 |
| rs532449151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244995 | TAAATATACTACAGT[A/G]CATATACTCGTATTC | 57630 |
| rs532449448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208997 | AAACAAAATAAAAAA[C/T]GAGGCAGTAGGACAG | 57630 |
| rs532485322 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161866 | AAGTAGAAAAATGGG[C/T]GGAAGAAACAATTTT | 57630 |
| rs532501248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138255 | AGTGGCCTGAACCTC[A/T]CTGTAGAGCTCTAAT | 57630 |
| rs532511941 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208058 | ATCTGGGGGTAGGAT[A/G/T]CTATGCACTAGGTAA | 57630 |
| rs532555846 | snp | A/C | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095568 | CATCACTTACCACCA[A/C]TATCTCACAAATGTT | 57630 |
| rs532565110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231718 | CCACTATGCATTACT[A/G]CTCCCTTCCAAATCA | 57630 |
| rs532572304 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123411 | TAATTTTTTGCTAAA[A/G]CGACTTTCAATAAAG | 57630 |
| rs532577834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137890 | AATTCAGGTGGCTTG[C/T]CTCATCTATAATTAG | 57630 |
| rs532596780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252613 | TCAAACTGTGAATCA[A/G]TTTTTGCCTCAATCT | 57630 |
| rs532623067 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188398 | CACTCTCACTGTAAA[A/C]AATAGTGTCCACAAA | 57630 |
| rs532652254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100333 | GACTTCATTACCTTC[C/T]ACCTCGTCAAATATC | 57630 |
| rs532657329 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238963 | TTCAAAGCTAATTTC[C/T]GCCCCCCCCCACCCC | 57630 |
| rs532659961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252092 | GATGTGCTAGGTAAA[C/G]GCAATTCACTCTTGT | 57630 |
| rs532671129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107666 | TCCTATCTCTAATTA[A/C]TGTAAGAGAGCTGAC | 57630 |
| rs532690584 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114866 | CCCTTAACCATTTAA[A/G]TAGAACGACATACAT | 57630 |
| rs532709835 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143850 | AAACAAAATAAACTA[C/G]AATTTTCTTGTTCAG | 57630 |
| rs532748583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240909 | TCATTGCAAGGAAGC[C/G]TTTTAAGTGAAGTGA | 57630 |
| rs532777779 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248950 | GAGGCAATTAGGGAC[A/C/G]GGCCCAGTGGCTCAC | 57630 |
| rs532781287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180204 | TCCAATTTCTAATAC[A/G]GTATGTCCCAACTTG | 57630 |
| rs532790095 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125178 | ACAGTGTTACATCAC[C/T]GAAGGAGCATGGCCT | 57630 |
| rs532804873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150857 | CTAAGCCATAGAGTA[C/T]TGCTACCATTAATTT | 57630 |
| rs532830730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187805 | ACACGTTGTCCATCC[C/T]CCTGCAAATTCATAT | 57630 |
| rs532842900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203784 | TTATCTTCTCTTCCA[A/T]ACTCCCTACAAGATA | 57630 |
| rs532868862 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151359 | CCATCACTGACATTG[C/T]TCTTGCTGGTACCAG | 57630 |
| rs532898001 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131506 | CTGTGAACCAAAGTC[-/T]TATTTCCAACCTATT | 57630 |
| rs532934451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168443 | AGAGAGAGATAAAGA[C/T]GATAAAAGTGTTGGA | 57630 |
| rs532955502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235008 | TACCCCCATTGAGAA[C/T]CACTGTTTTAGAGGG | 57630 |
| rs532959605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197295 | ACATGAGGCACCACG[C/T]CCAGCCAATTCTATA | 57630 |
| rs533044433 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263705 | TCATTACCTATCCCT[C/T]GAGTAATGCCTTAGG | 57630 |
| rs533044976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103263 | TTAGATGTATGAGAT[A/C]GGGTCATGGTTTGAG | 57630 |
| rs533053043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141631 | TTTCTTATAGACTGA[C/T]ATAAATACTTTTTTT | 57630 |
| rs533095621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096746 | ATTTTAAAAAATGGT[A/G]TACTGTTAGTCTGCA | 57630 |
| rs533121164 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197748 | ACTGACACTTTTTTT[A/T]ATAAAATCACAAATT | 57630 |
| rs533125760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256475 | TTTATGAACAGCTTG[A/G]GTATCTGAAGTTTAA | 57630 |
| rs533145677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155731 | GGATTAAATGTTTTC[A/G]TGAATTAAACGGTAG | 57630 |
| rs533147293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227536 | TGGAGCCCACAGCAA[C/T]AGAATGTTTAAAATC | 57630 |
| rs533152181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160876 | AAAGATAAAGCCAAA[A/G]CAATTGGTTTGATAG | 57630 |
| rs533169426 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254888 | ATGAGGACATGTAAA[C/T]GAAACTCAGTTATTC | 57630 |
| rs533172385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191724 | AACAGAATAGAGAAC[C/T]CAGAAATAAACCCAA | 57630 |
| rs533183623 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183788 | ACAGAACAAAAAAAA[A/C]TGGAAAAAAAAAGTC | 57630 |
| rs533186234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264267 | GGCATCTTCTCCATG[C/T]GTCTTCACATGGTCT | 57630 |
| rs533205544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156306 | GTTCACACAAAACTT[G/T]TATTTTTTTTTGCAA | 57630 |
| rs533208808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169111 | TATGTGCATATTACT[A/G]TTACTGTTCTTCAAA | 57630 |
| rs533214699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153632 | CTTTATTCCCCTAAG[A/G]GCTAAACTAGGTGTC | 57630 |
| rs533243609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111015 | TGTACTAATCAAAAA[A/T]TTTTTTTTCAGACCA | 57630 |
| rs533262277 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271857 | GTCTGACCTCAGGTG[C/G]GCTGGCACCGCAAAG | 57630 |
| rs533316988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133959 | AATGGTCTTACATGA[A/G]CCATTTCCCCATACG | 57630 |
| rs533329100 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172726 | GGTGTTGCCAGAGGA[A/G]ACTGACATTTGACTG | 57630 |
| rs533331527 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169528 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 57630 |
| rs533369036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213597 | TCTAAAATGTCACCA[C/T]CAAATCTAAGTTCAT | 57630 |
| rs533378011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199355 | GTCTAATGTTTGGTT[A/G]GCAGGTGGTTTTCCT | 57630 |
| rs533379141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104794 | CAATCCCAGCTACTC[A/G]GAAAGCAGAGGCAGG | 57630 |
| rs533397583 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272952 | TTATTTTGGTTTCCT[A/C]TGTATTTTTAGAGAG | 57630 |
| rs533418750 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194462 | AATGTTATTTAAATG[C/G]ATCATGCAGGCTGTA | 57630 |
| rs533431419 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250926 | TAAAAGCTGACCTTC[C/T]TTCCAGGCAGGGCAA | 57630 |
| rs533446451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119859 | TGTATATTAAACGGC[C/T]GGTGGTCAAAAACTA | 57630 |
| rs533453110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257194 | CCAGACACTTTCTGT[A/C]CAGCAGGAATCACAG | 57630 |
| rs533453551 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187713 | AAGCTAATGTCAGAT[A/G]TAAAAAGTTACCAGT | 57630 |
| rs533462434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176146 | TTTCCAGCGTCCAGA[A/C]CTGTGAGAAATAAAT | 57630 |
| rs533522703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226849 | ATCTAAATTGTACTA[C/T]CTCAGTCACCTAACT | 57630 |
| rs533552821 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251033 | TAAGCTGAGGAGATA[A/C]GGTGGAGGAAAAGGG | 57630 |
| rs533576168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118499 | CAGAGTCTCACTGTT[C/G]CCCAGGCTGGAGTGG | 57630 |
| rs533584609 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166268 | TTCTTTCCCATCTTG[C/G]CAGATGGTGGTGAAA | 57630 |
| rs533590547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233844 | GAAAATCTAGCTTTC[A/T]GGTAAGTCTGAGGGT | 57630 |
| rs533648024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206441 | ACTTTGGGAAGCCAA[A/G]GTGGGAGGATGGCTT | 57630 |
| rs533680255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197351 | CCCACCCAGCAGGGC[A/G]CAGAGGCTTACGACT | 57630 |
| rs533684988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249907 | ATTAATCATCAGGCT[C/T]CAGACACTCAACAGA | 57630 |
| rs533688766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162909 | CTGTGCTGTCTGCTG[C/T]CCTGCTCACGCTCAT | 57630 |
| rs533713754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205504 | AAAACTGCAGGCCAA[C/T]TTCCAGGCATGTCAA | 57630 |
| rs533752348 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133586 | AGTTCGAGACCAGCC[C/T]GGCCAACATGGTGAA | 57630 |
| rs533760376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234507 | GTTCGTTTGGGTGAA[A/G]AACATTTACATCTAA | 57630 |
| rs533771777 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260385 | CCGGCTCCCCACTGC[A/G]CCTCTTTTAGCCACT | 57630 |
| rs533787641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220970 | TTTAGCAGACAAACA[A/G]TTCTGGTTTAGTTAA | 57630 |
| rs533848569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227636 | CATCTATGCATTATT[C/T]ATTTTACTATACTAC | 57630 |
| rs533856256 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135083 | CTCATACTTGTAATC[C/T]CACCACTTTGGGAGG | 57630 |
| rs533895147 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207412 | AGTCTAGGTGACTGA[-/G]TGAGACCCTGTCTCA | 57630 |
| rs533908774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242495 | TGCATAAAAATCTCC[C/T]GGGAAACTTGTTTGA | 57630 |
| rs533914461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141924 | TTCACGTCATTCTCC[A/G]GCCTCAGCCTCCTGA | 57630 |
| rs533919943 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133133 | GACCCACTTATATGG[C/T]GTAGACATGAGCTGG | 57630 |
| rs533929424 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190165 | ACACCTCAAGGAACC[A/G]GAGAAACAAGAACAA | 57630 |
| rs533937029 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104021 | TCTGAGCTAGCAATT[C/T]CTTCTTTTCAGATGA | 57630 |
| rs533940175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264384 | CCTTAACCCCCTCTT[C/T]AAAGGTCCTATCCCC | 57630 |
| rs533946221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103364 | ATTGAAAAATACTTC[C/T]GTGAAATTCTACCAG | 57630 |
| rs533962398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147057 | GAGCAACAGATGTAC[A/G]GTCTATTCATGGTGC | 57630 |
| rs533979301 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142708 | AGTCCAATGTTCCTT[C/T]CCCAGATAAGTCAGT | 57630 |
| rs533982224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134453 | AGATTATTGTCCACT[A/C]TCTTAAAGCTATTCC | 57630 |
| rs533991886 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245658 | ATAGTAAACCTCAGT[C/T]TCTGCTACAAATAAT | 57630 |
| rs534008614 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100314 | TGTCACTATCCTGGT[C/T]GATGACTTCATTACC | 57630 |
| rs534027913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140422 | CAAGCATTTGGTAAG[A/G]AGCTTTGATAAGACT | 57630 |
| rs534035975 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255930 | GAGCCACCATGCCAA[A/G]CTAATTTTTTTGTTT | 57630 |
| rs534045997 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127979 | AATCTGAAATCCGAA[A/T]TGCTCCAATGAGCAC | 57630 |
| rs534073609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175708 | CCCACCCAAAACCAC[C/T]AGACCATAAGCTCTA | 57630 |
| rs534084823 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111521 | CTGCCCACCCTGGTC[C/T]CCCAAACTTTTGGGA | 57630 |
| rs534134479 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270705 | CTCCGCTTCCGCAGG[A/T]CCTGATTCCCGGCCC | 57630 |
| rs534143289 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112629 | ATGTGATCTCCCAGG[A/G]AGCAGCCTAATGGCT | 57630 |
| rs534146857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104200 | AGAGTCTGGGCAAAG[C/T]GAACCATCACTCAAA | 57630 |
| rs534161458 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125953 | TCCACATTTGATCTA[C/T]AAGAAACAAGAGAGA | 57630 |
| rs534192288 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217718 | AGTTACTGTTTAATG[A/G]ATACAGAGTTTTAGC | 57630 |
| rs534243120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148570 | TTGTAGAAATAAAAT[C/T]ATTAAAAATATCCTT | 57630 |
| rs534257737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198158 | GCCTTATGGAAACAT[C/T]TGAAACAAGGTCCTC | 57630 |
| rs534303700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144849 | TCTAAGTCAAGCATA[A/G]AAGTCATGGGGATCG | 57630 |
| rs534344714 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252831 | AGGCATGTTAAATAA[A/T]TCCTAAACTGGCAAC | 57630 |
| rs534353497 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177345 | CAGCTTGTACACTAG[A/C]GAATCTTTATAATCA | 57630 |
| rs534357745 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232461 | TTCAAAAAGATCACA[A/G]GACTTGCCCAAAGTC | 57630 |
| rs534368344 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229470 | TGGTATACCACCCCC[A/C]CACCCAAAAAAAAAA | 57630 |
| rs534419831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185641 | TGGGAGTGGAGGGAG[A/G]TAAGCTGACTACAGT | 57630 |
| rs534428468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138745 | CTCATCATGATCATA[C/T]CTGGCTGGCCAAGTG | 57630 |
| rs534432914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229976 | TTTAGGAGGTGGAGA[C/T]GGGTGGATCACTTGA | 57630 |
| rs534443971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236167 | ATTCTTCTCTCCCTC[C/T]AGACACATGGCAGGA | 57630 |
| rs534446665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217375 | AAAGCTTGTCACTGG[A/G]CAACAGAGAACTGGT | 57630 |
| rs534463256 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155889 | TTTGTTTTAGATTGA[C/T]TCTCAGATGCTCCTC | 57630 |
| rs534473147 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192573 | CACTATGGAAAACAG[C/T]GTGGAGATTCCTTAA | 57630 |
| rs534473800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181054 | AAATCTGAAATGTAG[C/T]CTAACCCAGACACAG | 57630 |
| rs534488850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104865 | AAGATTGCACCACTG[C/T]ACTCCAGCCTGGGCA | 57630 |
| rs534507472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243070 | AGTCTTCAAACCCCT[A/T]CTCCCAAATCCATAC | 57630 |
| rs534527711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180419 | TAATAACACTGTAGC[A/T]TAACACACTGCCACA | 57630 |
| rs534545575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116063 | AAACACAGAGAAACA[C/T]GAGCTCTAGATAAGA | 57630 |
| rs534546173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192162 | CTGACAAAGGACTAA[C/T]ATCCAGAATCTACAA | 57630 |
| rs534555367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239476 | CTAGTCACTGTTATT[C/T]AGTCCATATGTATGT | 57630 |
| rs534557009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101436 | AGAGAAAGTAGAAGG[A/G]TGGTTGCAGGGCCTG | 57630 |
| rs534576360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246409 | TATCAAACTGAGCTA[A/G]GAGTATGTGCAACCC | 57630 |
| rs534605493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107893 | TTTTAAGGAAAGCTT[C/T]AGTATATTTATAAAC | 57630 |
| rs534606349 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191963 | ACACTGGAAAAAAAA[A/C]CCTTCTAGACATTGG | 57630 |
| rs534637238 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207769 | TTAGAAAGCTCCCTT[A/T]TTCTTAACTCCTTGT | 57630 |
| rs534664865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166760 | GAGAATGGTTTTCCC[A/G]AAGCAGCTGGCTACC | 57630 |
| rs534689515 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095288 | CATGCCTTAGCCAGA[A/G]AGGGAGCGAGTGCAC | 57630 |
| rs534689520 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159404 | AGAGAGAGAGAAAGA[-/G]GAGAGAACTGGCAAG | 57630 |
| rs534713398 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111098 | GGATCACTTGAGGCC[A/C]GGAGTTCAGGACCAC | 57630 |
| rs534724540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131085 | TCCCACACATTGAAA[A/G]AAAGATTGTCAGGAC | 57630 |
| rs534733486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208453 | TACTGTGATAAAATT[A/G]TACTTCTTTTTAGTA | 57630 |
| rs534736922 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265171 | ACATTCAAAACCTAA[C/T]GTGTCTCTCCCACAA | 57630 |
| rs534739882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109694 | AACCAACAGCAGAAA[C/T]GAAAACTAAATGAAT | 57630 |
| rs534786950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232015 | CGGCCTCCACTGAAG[A/G]GAGAGAGCACCAGGC | 57630 |
| rs534803649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102618 | TCTTTGCAATTTCCT[A/C]ATTATTTTTTTCTCA | 57630 |
| rs534827305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150555 | TACTGTTATTAACTA[C/T]AGTCACCCTATAGAA | 57630 |
| rs534828259 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224252 | AGTGTAAGGAAGAAG[A/C]CAGTAGAGAGCTATA | 57630 |
| rs534836001 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170581 | ACATGTTCACCAGGC[A/T]GTGAGCTATGTGAGG | 57630 |
| rs534843569 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195966 | TTACAGGTGTGCACC[A/C]TTATGACCAGGTAAT | 57630 |
| rs534849134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107347 | GTATATGGGGCCTTA[C/T]GGTTTCAATGTTCGG | 57630 |
| rs534873679 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262539 | AGGCATGGCGGTAGG[C/T]GCCTGTAATCCCAGC | 57630 |
| rs534877168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131533 | TATTTCTAACGGGAA[A/G]CACACTGGTTTCAAA | 57630 |
| rs534888432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203947 | TACTTTTTACAAAAC[A/G]GGAATAAACTTTTTA | 57630 |
| rs534892128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196523 | GATATTATTAACATA[C/T]TCTTCCAGGGAATTT | 57630 |
| rs534911076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100793 | CTTTTTACACAGCTG[C/T]AGCTACTACTATCAC | 57630 |
| rs534949566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203269 | AAATATCCCAGAACT[G/T]GCCAAGCACGGTGGC | 57630 |
| rs534956282 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194474 | ATGGATCATGCAGGC[A/T]GTATTCTTTTGTGTC | 57630 |
| rs534974487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109153 | AGTCAGCTGCAACTT[A/C]CAGCTATTCTTGCCA | 57630 |
| rs534983915 | snp | C/T | 3.31609e-05 | 0.00407177 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117486 | TAGGCAGGTAAGCCC[C/T]TTATCCTGATATGTT | 57630 |
| rs535030990 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261179 | AGCCCAGAGAAACCC[C/T]ACAGCCAGCCCATGG | 57630 |
| rs535108346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247184 | GGCCAGAAGAGGACA[A/G]TGGAGAGGGTCAAGA | 57630 |
| rs535124832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139549 | CCTCCTTTCCTGTCT[G/T]CCTTCCTTCCAATAG | 57630 |
| rs535135568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225145 | AGTTAATGACCAGCT[G/T]ACCCTGAGATTTAAC | 57630 |
| rs535138628 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261939 | TATTTTTCTTACACT[A/G]AGTATTTTTTAAACA | 57630 |
| rs535140269 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181654 | GATACCTGAGTGTGT[-/A]AAAAATCCTCCCAAC | 57630 |
| rs535141175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153807 | CATTTGAAAGAAAAG[A/C]AGCAGAATGAAAATA | 57630 |
| rs535185829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132287 | CATTTCTCTAAAAGC[C/G]CAGAGTGGGAGACAG | 57630 |
| rs535197612 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256835 | CTCAAACTCCTGGCC[A/G]CAACTGATCCTCCCA | 57630 |
| rs535232272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108063 | GCTAGGAAAATCAGA[C/T]GTCAAGAGAGTGCTC | 57630 |
| rs535232645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210312 | ATTTGCATTTGAAAA[C/G]TGAACTTTACCTTCT | 57630 |
| rs535233775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269859 | TTAATTTTGCCCAAC[C/G]AAAAAGAGCTGAAGG | 57630 |
| rs535243654 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195675 | TCAGCTCTTTTTCAG[G/T]GTGTTAATCTTTTCT | 57630 |
| rs535262934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248213 | CTGCAGCACTATCTA[C/T]AATAGCAAAGACTTG | 57630 |
| rs535264556 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255049 | AATTTATGTTTAACA[C/G]AAAAAAGAACCTCCT | 57630 |
| rs535266687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124262 | TAAAATCATCTATTA[C/T]AGCTTAACTTTATTA | 57630 |
| rs535277268 | in-del | -/GCCATTT | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131759 | TTCTGTAACCAATCA[-/GCCATTT]GCATAGGAGTATAAC | 57630 |
| rs535289080 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108815 | TATATACCTCTCTAT[C/T]TCACCCAGTGCCTAG | 57630 |
| rs535324350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145005 | CAACCATCCAACCAA[C/T]GACCCAGAAATGAAA | 57630 |
| rs535330434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232898 | ACTAGTCTACTGATC[A/G]GTAGTGTGAACTGCC | 57630 |
| rs535331570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116955 | TTCTACAGTGTCAAG[A/C]GATGTCTCCCTCTAG | 57630 |
| rs535346871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152367 | CCCCTACTCACTTCT[C/T]CCAACCAGACTCTCC | 57630 |
| rs535362801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159726 | CCTCTTTACCAGTGA[A/C]ATGGGGCACCTGACA | 57630 |
| rs535366364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240477 | CTCTGGGATTACAGA[A/G]CGTGAGCCCTTGCAT | 57630 |
| rs535425150 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095357 | AGAGAACACTGTTTA[C/T]TTTTACACCTCCTGA | 57630 |
| rs535438642 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193994 | AGAGTCTTTTTTTCA[C/T]GTTTGTGCCAGACTT | 57630 |
| rs535453057 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255163 | CCCAGTAGATGACCA[A/T]TTTCAAAAAATGTTC | 57630 |
| rs535482241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131642 | GAAAAGAAAACCTTA[A/C]CTTTCCACGCCTAAG | 57630 |
| rs535492565 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228144 | AGTACATATTCTAAA[C/T]GTATACCTTCTGCAA | 57630 |
| rs535548837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166886 | TCTGCAATGTAAAAA[C/T]CTCAAAACATCTTAC | 57630 |
| rs535639823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159409 | AGAGAGAAAGAGAGA[A/G]AACTGGCAAGTACTA | 57630 |
| rs535650960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172569 | TATTGTTTTTATTTG[G/T]AGATTAAGTATGATT | 57630 |
| rs535658429 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162462 | TTCCACAATAGTCCA[C/T]CTTTCATTTGTTCTT | 57630 |
| rs535660211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173605 | CTGGTGATCCTGAGG[A/C]GCTGTAGATCCTGGG | 57630 |
| rs535660626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190940 | AGTCAATAAATGTGA[C/T]ACACCACATAAACAG | 57630 |
| rs535670847 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131760 | TCTGTAACCAATCAG[C/T]CATTTGCATAGGAGT | 57630 |
| rs535707252 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202692 | GAAATAACACAATAA[C/T]TTTACCTAGCAACTT | 57630 |
| rs535717061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160473 | TTAGCCTAGGGTTAC[A/G]TTTCCGTGATGCAAC | 57630 |
| rs535717558 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170169 | AGCCAGTTGCAGCAA[C/G]CCCAGACCCAAATGT | 57630 |
| rs535720830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181093 | CATATAAAATTCGAA[C/T]GTTCTTAGACATACT | 57630 |
| rs535729395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189825 | AATGCTACTCAAGTC[C/T]ACTACACTCAATAAA | 57630 |
| rs535765590 | snp | C/T | 2.58548e-05 | 0.00359538 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130160 | ACTTATATGAACCTG[C/T]CGAGAAAAGAAAAGT | 57630 |
| rs535776647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161122 | TCACTTGGCTACACA[C/T]GAAAGGGATGCTTAA | 57630 |
| rs535792749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188909 | TAGTTTATCAATGTA[C/T]CACTTGTAACTGACT | 57630 |
| rs535793601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102689 | TCTGCTGTCATCAAT[C/T]ATACATTTTCTGCCT | 57630 |
| rs535813467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163692 | CCATTTGGATTGTCT[A/G]TTCCACCTCATATTT | 57630 |
| rs535830711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105868 | TGAAGCCTGCGCAAC[A/C]GAGCAAGACCCTGTC | 57630 |
| rs535839456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203304 | GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCTGAG | 57630 |
| rs535846583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212321 | TGCCTGCCTCAGCCT[C/T]CCAAAATGCCAGGAT | 57630 |
| rs535851458 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153688 | TACCAGGAAGTTCAA[A/T]CTGATGGCTTGACAT | 57630 |
| rs535854013 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136233 | TCAAAATAAGCAATG[C/T]TTGTCAGCCAGTGAG | 57630 |
| rs535862565 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104057 | ACAGCAGGAGCCTGC[C/T]GTTAGAAAGGAGCCC | 57630 |
| rs535865232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103539 | CCTTCATTTTCAGCA[C/T]TGAGCACTTTTTATT | 57630 |
| rs535874879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163176 | TCCCTGGGCTGTACT[C/T]TCATCATTAATCATT | 57630 |
| rs535877555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254594 | CACTCGAGAGATGGG[A/G]GAAACTGAATTTATC | 57630 |
| rs535878117 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182614 | ATCCAACCTTGCTCT[A/C]ATATGACTTATAAAA | 57630 |
| rs535905089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220138 | CATTGTCTATAGGTA[A/G]CTTAGAAAAGAGTAA | 57630 |
| rs535921598 | in-del | -/C | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131346 | CTAAAAAGAGTTTCT[-/C]CCCCAAACCCAGTTT | 57630 |
| rs535927844 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214693 | TATGTGTATATATAT[A/G]TAAGTATTCATTCTT | 57630 |
| rs535942117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265221 | AGCTAAGAATGGTTT[C/G]TCTACCATTACCTAT | 57630 |
| rs535944477 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261747 | TTCTATTCAATTTTT[C/T]GTCTGAAAGAAAACA | 57630 |
| rs535961506 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147848 | TTTTTTACACGATAT[A/T]AGACATGACTTAACA | 57630 |
| rs535968650 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140592 | ATAAATAAATATGAG[A/C]TGAAATACTGACAAA | 57630 |
| rs535986181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150971 | AGCTGGTCTGAAGAA[C/T]GTAACATCCTGACGT | 57630 |
| rs535992220 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110285 | TTAAGACCAGGAGTT[C/G]AGGCTGCAGTGAGGT | 57630 |
| rs536006053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100492 | GATTACAGGTGTGTG[C/G]CATCATGCCCGACTA | 57630 |
| rs536028294 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236832 | TATGTAGGCTCAAAG[A/C/G]CTAACAAATAATTCA | 57630 |
| rs536029467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233889 | GATTTCTCTATTTCC[A/G]CCCCTGCCTCAGAGC | 57630 |
| rs536041569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241603 | CAGTGAGAAAGCCAG[C/T]GTGCCCTGGAGTAGG | 57630 |
| rs536102847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241098 | AGCCAAGCGTGGTGG[C/T]GGGCGCCTGTAGTCC | 57630 |
| rs536102952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249057 | TCGGTGAAACCCCAT[C/T]TCTACTAAAAATACA | 57630 |
| rs536115737 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200498 | AAATAAATATTTACT[A/T]CAGAAAAAAGAAGTA | 57630 |
| rs536153915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109809 | GAGCCCAGGAGTTCA[A/G]GACCAGCCTGGGCAA | 57630 |
| rs536159046 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147888 | TTAAAATGAATCTAT[C/T]CTGCTTATTAAAGCT | 57630 |
| rs536165888 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248953 | GCAATTAGGGACGGG[A/C]CCAGTGGCTCACGCC | 57630 |
| rs536166156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248685 | AAAAGTAATAGGAAA[A/G]GGGGAAACATCCACG | 57630 |
| rs536188037 | snp | A/C | 6.80249e-05 | 0.00583162 | missense | SH3RF1 | GRCh38.p7 | 4:169136434 | AGTGGCGGTTCTGGG[A/C]TGCCTGGGAGGACTT | 57630 |
| rs536198179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258570 | CAGACTTCAACTGTG[A/G]CAGAAAAAAAGCATA | 57630 |
| rs536211213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180236 | AAAGGGATTACCCAC[A/G]AAGAATAAAGAGGTA | 57630 |
| rs536225117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224071 | GTATTTAGCATCATG[A/G]CCCTTGTGGCACTAA | 57630 |
| rs536227418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130690 | AGACATGCTTAGAGC[A/G]GGCAATTACTTATAA | 57630 |
| rs536228481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169842 | AAGCAATCCTCCTGT[C/T]GTAGCCTCCTGAATA | 57630 |
| rs536237649 | in-del | -/TGTCTACCAACATGCCTCATTTTTCAT | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220099 | TCAAAGTGAATCATC[-/TGTCTACCAACATGCCTCATTTTTCAT]TGTCTATAGGTAACT | 57630 |
| rs536238904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157179 | AGTTCGGCTTTTAGG[A/C]AAATCTCTTCCTGAT | 57630 |
| rs536257300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265849 | TTACTTAATGATTCC[C/T]TAAATCATTGGAACT | 57630 |
| rs536286341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123349 | ACTGAGTGGAAAAAA[A/T]TTTCAAATTTCTAGA | 57630 |
| rs536329298 | in-del | -/TATTCTGTCTA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114518 | TCCTTGGGGAGTCAC[-/TATTCTGTCTA]TCACAAGTACCTTTC | 57630 |
| rs536391556 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186870 | AAAAAAAAAATTAGC[A/G]GGGCGTGGTGGCGGG | 57630 |
| rs536397043 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193979 | GACAATCTCAAGGAT[A/G]GAGTCTTTTTTTCAT | 57630 |
| rs536397503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261005 | CACTCATTTATTCAA[C/T]AAACCTCTTGTGAGT | 57630 |
| rs536401133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252958 | CCAAATACTGACCTG[A/G]TACCATGAAACTGGA | 57630 |
| rs536418844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245150 | TTATATTTACCACAA[C/T]AAGAAGAGTAACTTG | 57630 |
| rs536441410 | in-del | -/T | 0.475525 | 0.107882 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208149 | ATTTAAGTCCTCAAG[-/T]TTTTTTTTTTTTTTC | 57630 |
| rs536445086 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221231 | TATTCTTTTTGTCAT[G/T]TTTCTTTCAAGTGGA | 57630 |
| rs536452442 | in-del | -/T | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106461 | ACTAGCAGGAAACGA[-/T]GTAAATTTTTAATAA | 57630 |
| rs536480422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244169 | TTAAGACATTTATTT[C/T]AATCTGTCTTGCTGT | 57630 |
| rs536541021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251642 | GGATTGTGAGAAATG[C/G]AATGCACTGGGAGCG | 57630 |
| rs536569076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216586 | TTGCTCACCTCTATA[A/G]TCCGAGAACTATGGG | 57630 |
| rs536584069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207650 | TCATTCTTGAGGCAG[G/T]CCAGGTTCTGGATGC | 57630 |
| rs536607467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171796 | AGAGAAATGAAATGT[A/G]ATACAAGAAATGTGG | 57630 |
| rs536623108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122648 | CTGCTTGCTAGGAAT[G/T]AATTTGTGATTGTTT | 57630 |
| rs536633426 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265755 | TGCTGGGATTATAGG[C/T]GTGAGCCACCACACC | 57630 |
| rs536640225 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157923 | TTTTTGTATTTTTAC[A/G]AAATGGGGTCTCGCC | 57630 |
| rs536650242 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177193 | CAAATAAGGGATGGT[A/G]TGGCATCCTGTGTCA | 57630 |
| rs536681931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164338 | GGTTAAGTGGAAAAA[G/T]AACACATCTAAAGGA | 57630 |
| rs536684039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259455 | GCTGTGTTTACAGCC[A/G]CCCATATGTCACCAT | 57630 |
| rs536733512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187251 | TCACCCAGGCTAGAG[C/T]GCAGTGGTGTAATCT | 57630 |
| rs536752641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175687 | TTTATCATGACTAGG[C/G]ACCGACCCACCCAAA | 57630 |
| rs536757744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237490 | TATTTTTAATTTTTT[A/T]AAAAAGAGAGGCTGA | 57630 |
| rs536764775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144630 | TCTGCATAGCTTGGG[A/C]AGTTGAGGTCAATGA | 57630 |
| rs536824677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136263 | GCAAACATGTTTGTA[A/G]GTTGATCCTTTTGTG | 57630 |
| rs536828481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230944 | TTTATAGCCCTCAAG[A/T]ATAAACAATAGGCTC | 57630 |
| rs536836779 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238548 | TTATGAATTGTTGTC[C/T]ATCAGGCTGAAGTGA | 57630 |
| rs536858354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187361 | CCATGCTTGGCTAAT[G/T]TTTTAACTTTTTGTG | 57630 |
| rs536878205 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165302 | CTGCTTGCATCTTAT[A/C]TAATCCTACAGAAAT | 57630 |
| rs536886653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260310 | AGAAGACAACCCAGA[A/G]AAGCAGTTTTAGGAA | 57630 |
| rs536892268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136952 | CTCACTGTGAAATTT[C/T]GAGAAGAGCAATCAA | 57630 |
| rs536908014 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235611 | GTGTTATGCTACATT[C/G]CTTCTCATATAATAA | 57630 |
| rs536913624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157236 | TTACTCTTTCATGAG[C/T]TCAATGAGTATTTAA | 57630 |
| rs536945541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115309 | AACCAGGCCGCACAG[C/T]AGGAGGTGAGCTGCA | 57630 |
| rs536964185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130270 | ATCTGTACTTTCTGT[C/T]ATTTGGGGAAGGTAG | 57630 |
| rs536973492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150566 | ACTATAGTCACCCTA[C/T]AGAACTCTTGAACTT | 57630 |
| rs536985804 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151185 | CGCTGTGCAAAGACC[A/C]TGCGGAACCGGCCCT | 57630 |
| rs537038969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208289 | ACCCACTTTATCTTC[C/T]ATAGGAATTTCATTC | 57630 |
| rs537041670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151087 | TCTACAAACATGTTT[G/T]TTTTGAGTTTAGAAC | 57630 |
| rs537057329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100719 | AGCTTTACAATGCCT[A/G]TGAGCAAGGTTAATC | 57630 |
| rs537075144 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108195 | CTCTGAATGGAAGCA[A/C]TGCTTGAAAATGAAA | 57630 |
| rs537110178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207752 | CTACGTAAGACACTT[A/G]TTTAGAAAGCTCCCT | 57630 |
| rs537111999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216308 | GAAATTATAATGTTT[C/T]AGAAATTATAATTGT | 57630 |
| rs537132979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180373 | CTCCACCTCATTGAA[C/T]TGTTGACATTACATA | 57630 |
| rs537136975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108947 | GAAATAAAGGATATG[C/T]TGGATTCCCCAGATC | 57630 |
| rs537146188 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261347 | ATAGGAAGCAAGGAC[A/C]GTGAGGAAAGAATAA | 57630 |
| rs537162913 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137120 | TTCAAAATGAACTCA[C/T]GTGCTTCCATGTATA | 57630 |
| rs537173515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215762 | TTTTCTAATAGTCAA[A/G]TAATGTATTTTTTGT | 57630 |
| rs537181064 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235205 | AATGGAAATTTTAAA[A/C]ACTAAACAGTACCCA | 57630 |
| rs537235875 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232793 | TTACCCCTCTTCAGT[A/G]ATACACTTCAAAGCC | 57630 |
| rs537267840 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149543 | TATGGTGCTAAGCAA[C/T]GAGTAATTCTCCCTT | 57630 |
| rs537286989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237656 | CTGCAGTGAGTTCTG[C/G]ACAGATTTCAAAACT | 57630 |
| rs537306071 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113149 | AGAGTCTCACTCTGT[G/T]GCCCAGGCTGGAGTG | 57630 |
| rs537322809 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194007 | CATGTTTGTGCCAGA[C/T]TTGTAAAAAGGGGCT | 57630 |
| rs537350438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245280 | AAGAAGAAAATAAAA[C/T]GGAACTTCCTCTTCT | 57630 |
| rs537376722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209754 | TGTTGGTGCAATTCA[C/T]GCCATGCAATAAATG | 57630 |
| rs537400736 | snp | C/T | 0.000888434 | 0.0210577 | missense | SH3RF1 | GRCh38.p7 | 4:169268882 | GGGAGCTCTGCAGAT[C/T]TTTTGAGCTACAATT | 57630 |
| rs537400886 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260354 | GACTGCTTTCCTGCT[C/T]CCCCTGTCTGTTCTA | 57630 |
| rs537403297 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114129 | GTACTAGATGGTGCC[A/G]TAACAGGTTAACTCA | 57630 |
| rs537406989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124177 | TCCATTTAAATCTTT[C/T]TAAGCTCAATCTCAA | 57630 |
| rs537413611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165577 | GCCTGTAGTCCAATA[C/T]TGTGCCACTGCACTC | 57630 |
| rs537458551 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198797 | AGAAATAACAATTAG[C/G]CTGAAAACAGACTTC | 57630 |
| rs537461928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268092 | ATTTCTAATAAATAC[A/C]GAAATTTTGTGTGAC | 57630 |
| rs537477803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172323 | GGACTGTACTATCAT[A/G]AGTAATTCCTCCTTA | 57630 |
| rs537529558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184171 | ACTGTGAACCGACAT[A/C]CCCTACTTCTGAAAT | 57630 |
| rs537548355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112702 | CCATAACAAAGAACA[C/T]AACGTGGCCCATAGC | 57630 |
| rs537564193 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231514 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 57630 |
| rs537594187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191323 | AAAAAAAACCTTAGG[A/G]ATATACCTAACCAAG | 57630 |
| rs537598698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183337 | CCAGGCTGGAGTTCA[A/G]TGGCGTGATCCTGGC | 57630 |
| rs537617071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130313 | TCTGCTCAACCCAAA[C/T]TTACCAGTGACCTAA | 57630 |
| rs537618010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250068 | TTTCCACCCACTCCT[C/T]AAACAGTTTTAGGTA | 57630 |
| rs537622413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247321 | GGATCTTCCCCCAAA[C/T]AAATATTTACTGAGA | 57630 |
| rs537634160 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252072 | GCGACTCAAGAACCA[C/T]GTGAGATGTGCTAGG | 57630 |
| rs537681451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256641 | TCATTCTGTCACCCA[A/G]GCTGGAGTGCAGTGA | 57630 |
| rs537683751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253908 | ATAAGGCTTTTGACT[C/T]AACTCAGCAGAACAT | 57630 |
| rs537705675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213851 | GTCTATTTCTGGGCT[C/T]TCTAATCTAGTTCAT | 57630 |
| rs537760972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126963 | CCTTTATTGACCTGA[C/T]TACCTTATAATACCT | 57630 |
| rs537767531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221677 | TAAAATAAAGGCAAC[A/G]TATTTTATGTCTGAT | 57630 |
| rs537767836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213112 | TAAGAGACTGCCAAA[C/T]TGTCTTCCAAAGTGA | 57630 |
| rs537797889 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099295 | CATCTCACTATATTG[C/T]CCAGGCTGGTCTTGA | 57630 |
| rs537801646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263553 | CCTGGAGCAACTCAG[C/T]TGTCCTAACTTTCTC | 57630 |
| rs537819526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127576 | TGGGATGACAGACAG[A/G]TTTGTTTATAATTAG | 57630 |
| rs537828151 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135086 | ATACTTGTAATCCCA[A/C]CACTTTGGGAGGCCC | 57630 |
| rs537832254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236299 | AAGCCAGAACTCGAC[C/T]TGCCAATTCCCTTCC | 57630 |
| rs537895217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243179 | ATTACAACTACACAA[C/T]AAAAATACCAAAAGG | 57630 |
| rs537930486 | in-del | -/TTAA | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147998 | TAAAATATCATGGTT[-/TTAA]TTAGTTTGTGATTTT | 57630 |
| rs537957185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242610 | ACCCAAAATTCATGT[A/G]TTGGAAACTTAATCT | 57630 |
| rs537969771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155949 | CAAATGTACATCCTA[A/C]CGCTTTTCTCCACAA | 57630 |
| rs537980462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159373 | TAAAACACAGCAATC[A/G]ACAGAGAGAGAGAGA | 57630 |
| rs537987638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198918 | GAAAAATAATGACCT[A/G]TGTAGAAAGATAAAA | 57630 |
| rs538014480 | in-del | -/T | 0.499958 | 0.00459298 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224322 | GATCTAATTTCCTAT[-/T]TTTTTTTTTTTTTGA | 57630 |
| rs538068891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098323 | TAGCCTCGTGGGACC[C/T]ACTCCTGACTGAAAG | 57630 |
| rs538078785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170159 | TGGTTTACTAAGCCA[A/G]TTGCAGCAAGCCCAG | 57630 |
| rs538085799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133671 | AATCCCAGCTACTTG[A/G]GAGGCTGAGGCAGGA | 57630 |
| rs538113175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222912 | ATGAAGCCAAATGGG[C/T]GGCTATAAATGCCTG | 57630 |
| rs538169193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236601 | AGTAGCAACTACTTC[A/G]TAGTGTTGCTATGAG | 57630 |
| rs538221678 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112882 | GATGGCAAGAAGAAA[C/G]GGAAGGATAATCTTC | 57630 |
| rs538227128 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241541 | CTGGATGTGCTTTGG[C/T]GCAGTCCATAGCTAA | 57630 |
| rs538245400 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214057 | CACTGATATAGTTTG[A/G]ATGTCTGTCCCCTCC | 57630 |
| rs538250568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192634 | AGCAATCCCACTACT[A/G]GGTATCTACCCAAAG | 57630 |
| rs538259151 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124380 | AAATAAAATTTTGTA[A/G]TAAAATATAAAATCA | 57630 |
| rs538267937 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158693 | AGTTTAATATTTCCA[A/G]TGAAGTAGAGCAATA | 57630 |
| rs538273706 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177667 | TGTGTTAACTGTCTG[A/G]TCTACTAATTTAAAA | 57630 |
| rs538313815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192227 | TCATCAAAAAGTGGG[C/T]TCAGGACATGAATAG | 57630 |
| rs538337007 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176475 | TTAACCGAACAAAAC[A/C]AATATTAATTTTAAC | 57630 |
| rs538348189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250722 | ATTAAACAAATAAAT[G/T]TATAATGTGATTTTA | 57630 |
| rs538368437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206614 | TGCTTATTATGTGCA[A/G]TGTTCATCACTGCTG | 57630 |
| rs538432607 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156524 | CACAAAGTTGGTGGG[A/G]AAAAAGCCATGGATT | 57630 |
| rs538446624 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187000 | GCCTGGGGACAGAGC[A/G]AGGCTCCATCGCAAA | 57630 |
| rs538451246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207595 | CTGCCAAGACTAGAA[C/T]TCTGTCCATAGTATG | 57630 |
| rs538488311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230024 | TAGCCTGGTCAACAT[A/G]GTGAAACCCAGTCTC | 57630 |
| rs538503380 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127901 | GACCAGAAGTGTTTC[A/G]GATTTTGAATTTTTT | 57630 |
| rs538507247 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183711 | TATGGCTGTGCCACC[A/G]CACTGCAGCCTGAGC | 57630 |
| rs538510260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206767 | AAATGACATGTAGCG[C/T]TGCATTCATTTTACC | 57630 |
| rs538525047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186650 | AACTTAAAGGAGAGA[C/T]TCCCATCATATCAAT | 57630 |
| rs538538895 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108526 | ACCTATGGGCTAGAA[A/G]TGGGAAGAGAGGGTG | 57630 |
| rs538546126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142798 | TACATCCTCTCAGCA[A/G]ACATGAAAATATTTT | 57630 |
| rs538587765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185748 | CAGTCTTCAGAAGAG[C/T]CTGTGCTAATAACAG | 57630 |
| rs538592030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256699 | ACTCCTGGGCTCAAG[C/T]GATCCTCCAGCCTCA | 57630 |
| rs538597325 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127199 | TATTTAAAATTTTAA[C/G]TGTTACATGTGAAAT | 57630 |
| rs538626297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129516 | GTCATGTTTTCAGAA[A/G]GGAAATCAACATAAT | 57630 |
| rs538633936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230067 | AAAAATTAGCCAGGC[A/G]TGGTGGTGCATGCCT | 57630 |
| rs538634165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136815 | TCTATATCACAGGTA[A/G]ATATTAAATCAAGAA | 57630 |
| rs538635954 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262018 | TAAAAATACTATGAG[A/G]AAAATACTATGAAAA | 57630 |
| rs538637001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156056 | AGAATTTTACATATA[A/C]AATATGAAAGTAATG | 57630 |
| rs538649099 | in-del | -/GTAG | 0.480461 | 0.0968913 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157923 | TTTTGTATTTTTACA[-/GTAG]AAATGGGGTCTCGCC | 57630 |
| rs538688703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130177 | GAGAAAAGAAAAGTT[A/T]TTAAAAAGAAGACTA | 57630 |
| rs538694730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236638 | ATAAGTTAATATACA[C/T]AAAGTACCTAAAACA | 57630 |
| rs538702158 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156205 | CATCAACCAAGATAA[C/T]CTTTCATATAAGAAG | 57630 |
| rs538712131 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269777 | CATGCCTCATGTAAT[C/T]GCTCGTGGTAAATGA | 57630 |
| rs538749742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236323 | CCCTTCCTGGAAGCA[C/T]GTGCTGAGATGGAGC | 57630 |
| rs538763712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157114 | GGAAAAATTTAAACC[A/G]AATTTATTAATTTAC | 57630 |
| rs538802685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134230 | AGGGGTGGAATGGTT[A/G]AAGGGGAAACTTTTA | 57630 |
| rs538804028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259523 | TGGCAGACATATACG[C/T]GACAAAAGGATTGCA | 57630 |
| rs538811836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267752 | GGTATCCACATCTGC[A/G]AATTATGGGAACTAA | 57630 |
| rs538818760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246602 | AATTAGACTAATTGC[C/T]TCCCAATCTTAGCTG | 57630 |
| rs538855273 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181097 | TAAAATTCGAATGTT[C/G]TTAGACATACTATAC | 57630 |
| rs538868615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099845 | TTTTATAAACCTCTG[C/G]GGGGGCGGGTGGAAT | 57630 |
| rs538869813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258444 | CTTAATATTTCAGAC[C/T]TGTTTTACAAAAATG | 57630 |
| rs538903760 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219142 | ATGAGGAGCTGATAG[A/C]CGCAAGCATAAGAAC | 57630 |
| rs538917676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253383 | GTTAAATTGTTGATA[C/T]ATTAACAATCACAGA | 57630 |
| rs538924289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163092 | GTTTCGGGGGCAAGG[C/T]AGAGGGAGAGAAAAA | 57630 |
| rs538927388 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257522 | TACAGCTTCCCCCAT[C/G]CAGGCTTGCCTGACC | 57630 |
| rs538939440 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198373 | GTGTTAAATCAGCAG[A/C]TTCTTCATGCTTAAT | 57630 |
| rs538939630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120264 | TATTATAGAATTCAT[C/T]GTCAGAATTCAGAGG | 57630 |
| rs538941279 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128613 | CAATTATTTATAGAT[G/T]TATCAAGACAAAATA | 57630 |
| rs538952519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214516 | TCTATAGATCAAGTT[A/G]GGAAAAAAACTGACA | 57630 |
| rs538986156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178992 | AGTAGACCCTACCCA[A/T]GTGTGCTAGGCATAA | 57630 |
| rs538997128 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266051 | TTTGGCCTAAAACCA[A/G]CAGGAATTCTTTACT | 57630 |
| rs539027768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132520 | AAAGAATGACTAAAC[A/G]CAGAAGGACAAAAAG | 57630 |
| rs539055379 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256485 | GCTTGGGTATCTGAA[C/G]TTTAAGCCAGCTGTT | 57630 |
| rs539077731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190035 | AACTGAGTGACAATA[A/G]TGACACAAACTATCA | 57630 |
| rs539084397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133073 | GCCAGCAATTTGGAC[A/G]TGACAGTGACATCTC | 57630 |
| rs539088715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125234 | CCAACCCTGGCTCAG[A/C]CTCTTGGGGCAGTCC | 57630 |
| rs539103805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193135 | TTGGGGACTCAGGGG[A/G]AAAGAGTGGGAAGGG | 57630 |
| rs539112956 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155393 | TGCTTTTTGTTGTGA[A/G]GACTTCTTAATACTC | 57630 |
| rs539119365 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120230 | TCTATGCTATACTTA[A/C]AATTTTTATTTCTGA | 57630 |
| rs539133054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244064 | TGATTTAGCAACAGG[C/T]TTCTACATGCTCCTA | 57630 |
| rs539138691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196438 | ACAATGTTAGGTAAC[A/G]ATGTACTATATTTTT | 57630 |
| rs539148303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125834 | TACTGGTTGATGAGG[A/G]AATGGTTCAAGCTAC | 57630 |
| rs539152495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134249 | GGGAAACTTTTAATG[A/G]AACACAGAAAGAGCC | 57630 |
| rs539158523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239738 | AAAAGTAATTAAGAT[C/T]GGCCGAGTGCAGTGG | 57630 |
| rs539167090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248131 | GATCCAGCAATCCCA[C/T]TGGTGGATATATACC | 57630 |
| rs539188224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164378 | AAAAAGATGATTCTA[C/T]TGACAGGCTCAACAG | 57630 |
| rs539189600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203240 | TTGCTCTTTGTAGTT[G/T]AAAGAGCAAATAAAA | 57630 |
| rs539220358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167729 | CAAATGAGTGAAAGA[A/G]GGTGTGAGGGAAATT | 57630 |
| rs539238146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266970 | AAGGCTCAAGTTTAG[C/T]TGAGTTTCTTGGCAA | 57630 |
| rs539253583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220298 | AGTGGTGTCCACAGC[C/T]AGCTGACACTTCACA | 57630 |
| rs539259294 | in-del | -/GACTCAAGCAATCCTCCC | 0.0209421 | 0.100162 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174292 | CTCTCAAATTCTTAA[-/GACTCAAGCAATCCTCCC]GCCTCAGCCTCCCAA | 57630 |
| rs539272622 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143377 | AAACCCGGTGCGAAC[A/G]GAGTGCTTCCATCCC | 57630 |
| rs539273570 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102535 | ATATTTTTTTTCTTT[G/T]GAAGAAAAACCTGTC | 57630 |
| rs539276159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270643 | GGGAGACCGCGGCAC[A/G]GAGCCCTGGCAGCTT | 57630 |
| rs539298471 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241313 | TTTACACATTGAAAT[A/C]AATACTGGAAATACA | 57630 |
| rs539298725 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211888 | AGAGGGGGCTTTTCA[A/G]TGTAATGAAAATATC | 57630 |
| rs539305756 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146032 | ATAAAATATTACATA[G/T]TCTATATATTCTATA | 57630 |
| rs539313723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226705 | AACTATTGTAGATAA[C/T]AAAACCTATCTTTGT | 57630 |
| rs539327228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179681 | CTCCTGAGAGCCCCA[C/T]GCAAAGACAACACTG | 57630 |
| rs539333094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136234 | CAAAATAAGCAATGT[C/T]TGTCAGCCAGTGAGC | 57630 |
| rs539364191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139678 | TAGAACTGCTGGACC[A/G]TAGGGTTGGATGCTT | 57630 |
| rs539411402 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180296 | ACCTGTACAGAAAAA[C/T]GCACCCAAACCGGAG | 57630 |
| rs539421446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249214 | GCCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA | 57630 |
| rs539436041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147884 | TTAATTAAAATGAAT[C/T]TATTCTGCTTATTAA | 57630 |
| rs539450490 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182738 | AGGAGGCAAAGTGTT[C/T]AAGTGTAAAGAACGA | 57630 |
| rs539475802 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253024 | GACTGAGAAATTTAC[A/G]TATCAGGTTAATGTG | 57630 |
| rs539482929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255881 | CAAGCGTTCCTCCCC[A/C]CTCAGCTTCTGAAGT | 57630 |
| rs539501178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141465 | GCTAGATCAAAGTGT[A/T]AGTTTAAAAATCGTT | 57630 |
| rs539501417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148503 | CAAAATTATACACGA[A/T]GAGACTTAGGATTAT | 57630 |
| rs539511954 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221751 | TCATCTTTTACCCCA[C/G/T]AAAATTTGCCCTGAA | 57630 |
| rs539516997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189065 | CTTGTAGAAAAAAGA[C/T]AGTTTGGGCTTAAAT | 57630 |
| rs539541176 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263236 | GGTATTCTTTGACCA[C/T]GCACTTAATCCAAGG | 57630 |
| rs539541444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255213 | CCAAAACAGTACATG[A/C]ATATTTTAGCTACAA | 57630 |
| rs539562220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195623 | TCTATATTTTCCAGT[C/T]CTTTTCTTCTCCATA | 57630 |
| rs539570084 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189364 | GTATTCTATTTTGAC[C/G]AGTCCCACATGGGGC | 57630 |
| rs539644709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166958 | ATCAAGAAGGTGATA[A/T]CTTCGACACGGAAAA | 57630 |
| rs539657762 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106026 | TTTTTTTAGCTCATC[A/G]GCTATAATTAATGTT | 57630 |
| rs539658744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184198 | AAATCCATTTGGTAC[A/G]GCAGGAGATCTCTTG | 57630 |
| rs539667967 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175069 | ACTGTTCACCTCGTT[G/T]CTTGGGCCAAAAGAC | 57630 |
| rs539670760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139031 | TTCATTGCTCAGTGC[A/G]GCCTCGAACTCCTGG | 57630 |
| rs539700347 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269944 | CCCTTCAGGGCAGTA[C/G]TTGATAAACTCTGAA | 57630 |
| rs539708015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154001 | TCATGCATCACAAAC[C/T]AAGTATCAGCATGTA | 57630 |
| rs539725255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191391 | TGCTAAAAGAAATCA[C/T]AGATGACACAAACAA | 57630 |
| rs539729922 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182971 | AGGACTGCTTGAGGC[C/T]AGGGGTTTGAGACCC | 57630 |
| rs539733902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174392 | TCAAGCTTTAATGAG[C/G]GCACGAATCACCTGG | 57630 |
| rs539771133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154647 | TCTTAGTTAACCCTT[A/G]TTTATCCATCACACA | 57630 |
| rs539771339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147329 | GAGGTTATGAACATG[G/T]AATTGTCATTAATTC | 57630 |
| rs539804396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104148 | AAAGGAATGCACTGG[C/G]GGAGGGAGGCTGCAG | 57630 |
| rs539804438 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097098 | AGTAGCTGAGCAGGG[C/G]GGGTTCAGTCCTCTC | 57630 |
| rs539812194 | in-del | -/AT | 0.00240577 | 0.0345991 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134723 | CTTTTTCTCACACGG[-/AT]ATGATTAGTTAAATG | 57630 |
| rs539824094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219637 | CTACTGTTTTGTATT[C/T]CCTTCAGGCCTATTT | 57630 |
| rs539825083 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197559 | AACCCAGGAGGCAGA[C/T]GTTACAGTGAGCCAA | 57630 |
| rs539846223 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204732 | ATTTTTTGTATTTTA[G/T]TAGAGACGGGGTTTC | 57630 |
| rs539849005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269999 | AATCCCATTCAGAAA[A/G]GCTGGCAAAATTATC | 57630 |
| rs539855029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160697 | GTTTCTAAAAAGAAG[C/G]CTTCCCACATTAAAT | 57630 |
| rs539855473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248783 | ACACAGACAACAAAG[C/G]CTACTCCAGATTGAA | 57630 |
| rs539857757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161816 | AACTGAGGCACAAAG[A/C]AATCATAGTAATAGA | 57630 |
| rs539864595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097561 | CAGCTTGTAGGAAAC[A/G]AGAGGGAGGTGACTT | 57630 |
| rs539879807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110085 | GAACAAAGAAAATGA[A/G]CGTTAGAGGCCGGGC | 57630 |
| rs539882664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226084 | TATTCTGACTAATGC[C/T]ATTATTCTACTTAAT | 57630 |
| rs539907885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204104 | AGGAAAAAGAACTCA[A/T]GGGTAAGTAAAACTT | 57630 |
| rs539919488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153388 | AAGATATAAGAGAAT[A/T]ATTTACCAATTTTTG | 57630 |
| rs539922136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168340 | CTAGAATCTGACCTT[A/G]TTAGCACCAGTCAGT | 57630 |
| rs539927159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098125 | TGACCCACAGAAAGT[A/G]TGAAATAATACATGC | 57630 |
| rs539935674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141851 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 57630 |
| rs539943524 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102959 | TGGAGTCTCGCTCTG[C/T]CAGGCTGGATGGAGT | 57630 |
| rs540026043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227923 | TGTCACAAGAGCGAA[C/T]GAAGGGAACTCTACA | 57630 |
| rs540026193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235505 | GCACAGAACGGTTAA[A/G]TAACTTGCCCAGGGT | 57630 |
| rs540041402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192071 | ATACTAAAGAGCTTT[C/T]GCACAGCAAAAGAAA | 57630 |
| rs540051314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255283 | ATTAAAAAATATATA[A/C]ATTTATTGAAATTTG | 57630 |
| rs540074280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242419 | AAATATTAAATTCAT[A/G]TGTCCTAATAGCTAA | 57630 |
| rs540104432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198669 | TATATTAAGCAAAAC[A/G]ATTACTAAAGAGAAT | 57630 |
| rs540113859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254784 | CACTAAGAGCTCTTC[C/T]GGACCTGAACCCAAG | 57630 |
| rs540117159 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191205 | CCTCTTCAACATACA[A/G]AATTAATGTACGCAG | 57630 |
| rs540134238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103603 | TCCCTAAATTCTATA[C/T]TTGGTGGCTTTTAAT | 57630 |
| rs540181474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211912 | AAATATCAGAAAAAT[C/T]GCAAAAGTCACTGTT | 57630 |
| rs540224690 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261441 | ATGTTTGTCACTTAA[C/G]TCAACTGCAGGTAAG | 57630 |
| rs540253092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126563 | ATACACACATACAAA[C/T]ATGTATGTGTATAAA | 57630 |
| rs540263336 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184382 | GAAGATTCTAGAAAG[A/C]CAGATGGCAGGGCCA | 57630 |
| rs540275852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183405 | CCTGGCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 57630 |
| rs540300473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234267 | CATCTAGTGGGTAGA[C/T]ACCAGGTATGCTGTT | 57630 |
| rs540318004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110753 | TTATGTGGCCCACCT[A/G]TAGGAATGCTGGCTT | 57630 |
| rs540324164 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233078 | ACGTGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 57630 |
| rs540331181 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215445 | GTTTTGGTATTAGGT[C/T]AATGCTGGCCTCATA | 57630 |
| rs540334798 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211168 | TTTAGTATTATGACC[-/T]CATTCTCCAAAGAAG | 57630 |
| rs540340029 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243738 | ACTGGATATTCAAGA[A/C]GTCTTGCTTTCATTT | 57630 |
| rs540341638 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191130 | AATACTAAATGGGGA[A/G]AAGTTGAAATAATTC | 57630 |
| rs540356876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154123 | AGTGCTTGTAGTTTC[C/T]CATTACCCACAGTTA | 57630 |
| rs540364379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241186 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 57630 |
| rs540421886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204290 | CTTCTTTTAATCAAA[A/C]TAATTCAATGAATTT | 57630 |
| rs540427424 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272740 | CACACAGTAAGTAAT[A/G]TTGAACCAAGACTCA | 57630 |
| rs540433057 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256322 | GAGGAAGGAAGGGAG[A/G]GAGAAATAGAGGGAG | 57630 |
| rs540450875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161352 | TACATTTCAAATAAT[A/T]TTTGTTTCCAAATCA | 57630 |
| rs540481498 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212501 | GTATCTATATGTTTT[A/T]TCCCTTTTCATAATT | 57630 |
| rs540488556 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227166 | CAACACCCTGCCTTG[-/A]AAAAAAAAACACATA | 57630 |
| rs540492926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203603 | TTGCTCTGCAATCCC[C/T]ACCAGAAACAAGAAT | 57630 |
| rs540511917 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271669 | GTGGTGAATCGATGG[A/G]GACAGTGCCGCGGCC | 57630 |
| rs540542871 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188683 | CAAAATCTTTAAAGC[C/T]TTCTGGCTTATGTAA | 57630 |
| rs540556449 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222368 | TACTTGGGAGGCTGA[C/T]GCAGGAGAACTGCTT | 57630 |
| rs540556467 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160771 | ATCTTTGAAAGACTT[A/G]TTCCCACACAGACTG | 57630 |
| rs540571060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175373 | ATCATCTGGTCCCGG[C/T]TAACCTCTCTGGCTC | 57630 |
| rs540598553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227361 | TGTGCATTTGAAAAA[C/T]GTTCCTCTTGAATAA | 57630 |
| rs540641010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191483 | CCAAAAGCAATCTAC[A/G]AATTCAATGCAATCC | 57630 |
| rs540656700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137203 | CAGAAACTCTTAATA[C/T]GTTTTTTGTCATGTC | 57630 |
| rs540713552 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095087 | ATGACATCAAGGAAT[G/T]GATATAAAAAGACAG | 57630 |
| rs540745431 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212308 | ACCTCAGGTGATCTG[C/T]CTGCCTCAGCCTCCC | 57630 |
| rs540796821 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192917 | TATATATCATATATA[C/T]GTGATATATATATAT | 57630 |
| rs540807971 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221933 | AGTAATAATAGACTA[C/T]GTAATACAAACTTCT | 57630 |
| rs540827581 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138490 | ACACCTAGAAACAAA[A/T]CTTTGAAAGTGCAAA | 57630 |
| rs540839655 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216753 | TCCTTCTATTTATAT[G/T]TTTGACAATTTGATA | 57630 |
| rs540842542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172015 | GCTACAGAATAGAAT[C/G]TTATAAACTCTGACA | 57630 |
| rs540857312 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268135 | TGTCCAAATAATTAG[C/T]TTCATCTAAAATTAT | 57630 |
| rs540869656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221214 | AAGTCAAGTAGTGAT[C/T]TTATTCTTTTTGTCA | 57630 |
| rs540889368 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143643 | ACTGGCAGCAACTAC[A/G]AGGGTTACTCATTTA | 57630 |
| rs540907794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179869 | TGTATTTTTTTTCCT[A/G]AGACATATTCCACCC | 57630 |
| rs540912815 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197256 | ATCCACGTGCCTCAG[C/T]CACCCAAAGTGCTAG | 57630 |
| rs540961578 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123222 | TTCTAAACAGAGCTT[A/G]TACCAGTCATCTTAT | 57630 |
| rs540967262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179259 | GGAGAGGACCACAAG[A/C]CAAAGGATATTTCTT | 57630 |
| rs540971368 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107743 | TGGACGTGAGCCTTA[G/T]CATTTACAGGCAGTG | 57630 |
| rs540983941 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093940 | ATAGGTCTGCTTTTC[A/C]TTCTATGGCTAAGAC | 57630 |
| rs541004705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129922 | GAGATAATAGATGAA[A/C]GATAGATACCCACCT | 57630 |
| rs541009380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187460 | CCCAAAGTGCTGGGA[C/T]TACAGGCATGAGCCA | 57630 |
| rs541021943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101576 | CTCAATGCCACTGAA[C/T]TGTACACTTGAAAAA | 57630 |
| rs541045984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237033 | AAATATGCACACGCT[C/T]CCTTCTCAATGAACA | 57630 |
| rs541053466 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112257 | GGATCTCTAATACAC[-/T]TTTTCCTTGCTGATA | 57630 |
| rs541082399 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200931 | GGCCCTTTCAAAGTA[A/T]AATGACAGCAGTAAG | 57630 |
| rs541084819 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193426 | ACAAGGACTCCACCC[A/C]CAGAGAGTTATTTGG | 57630 |
| rs541095552 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186826 | CCTGGCTAACACGGT[A/G]AAACCCCATCTCTAC | 57630 |
| rs541098053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136687 | ATTCCCTGAGGTTTA[G/T]TTCCAACATGATTTC | 57630 |
| rs541122301 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095642 | AAATGACGCTTCATA[A/G]CCATTCTCAGACAGT | 57630 |
| rs541126801 | snp | A/C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250939 | TCCTTCCAGGCAGGG[A/C/T]AAAGACTAAGTGCAA | 57630 |
| rs541155351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200732 | TAACAGAAAGTTCCA[C/T]GGCTATTCACTCTTC | 57630 |
| rs541163139 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133882 | CAGATTTAGCAATGG[A/G]TCTCAGTTAAATCTA | 57630 |
| rs541174591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164861 | AGTTGATATGGCATT[C/T]CTCTTGGATGGCCTT | 57630 |
| rs541191635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217737 | CAGAGTTTTAGCTGG[C/G]GAAGCTAAAAAAACT | 57630 |
| rs541191747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139095 | TAGTTGGGACTATAG[A/G]TATGCAACACCACAC | 57630 |
| rs541192760 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175962 | GGGTGGAGGTCCCAT[A/G]ATGGGATTGCTGCCT | 57630 |
| rs541204511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224740 | CAGGAGATTATGACA[C/G]CTTGGCTTGGGTAGG | 57630 |
| rs541259660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100135 | GGCCCTTTACATCTG[C/T]TGCTCCACCCTCTGC | 57630 |
| rs541267986 | in-del | -/TTG | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099292 | TGGCATCTCACTATA[-/TTG]CCCAGGCTGGTCTTG | 57630 |
| rs541268541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189119 | CAGTTCAAGTAGAAG[C/T]TTTTGTAAATGTCTA | 57630 |
| rs541273680 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257380 | TAAACTTATGGCCCT[A/G]TTCGCCTCAGACAGT | 57630 |
| rs541279871 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225433 | CCACCAGAGAAAAGG[C/T]AGACCTCACAAAACA | 57630 |
| rs541298608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195744 | TTGTTTATTTTGGTT[A/T]TAATAATGTGCAGTT | 57630 |
| rs541334513 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223691 | TAATGGGGTGATGGG[A/C]AAGCATATCAACAAA | 57630 |
| rs541339185 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158558 | TAATGCACAAACAGA[A/C]TTAGGTCCTATGTGC | 57630 |
| rs541342883 | snp | A/G | 5.02046e-05 | 0.00500997 | missense | SH3RF1 | GRCh38.p7 | 4:169136544 | CTCTGGGCTGCTGCC[A/G]AGGAACATTCTCCAG | 57630 |
| rs541359543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195074 | ATCCTGCCTAAATAA[C/T]ATACTTTAACATTTC | 57630 |
| rs541361446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202915 | GGAAAACAATTTAAA[A/G]TGTATATATCTAAAG | 57630 |
| rs541374339 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203535 | CAGCCTGGGCAACAG[A/C]GCCAGACCCTGTCTC | 57630 |
| rs541428115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231657 | TAAGATTAGTTTTTG[C/T]TCAAAGCTGCTATAG | 57630 |
| rs541432393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145136 | AAACCTGTACTTGTA[C/T]GTTTATTGCAGCACT | 57630 |
| rs541433676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102146 | CCACTTACTGCTTTC[C/T]ACCAGTTGCCACAGC | 57630 |
| rs541446119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131170 | CCACTGGGGTAGGCC[C/T]GACCAAAGCCAGGCA | 57630 |
| rs541496970 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269385 | AAGGAGCCAAGAATC[-/A]AAAAAGTACCCAAAA | 57630 |
| rs541507220 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166909 | CATCTTACTGTTGCT[C/T]ACTTCAAGAAGAGGC | 57630 |
| rs541514224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252619 | TGTGAATCAATTTTT[A/G]CCTCAATCTATCTTT | 57630 |
| rs541519842 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194037 | TAGCCTACTACCTTC[A/G]TAGTCAGCATGAAAT | 57630 |
| rs541539203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209007 | AAAAATGAGGCAGTA[A/G]GACAGGGCGTGGTGG | 57630 |
| rs541549557 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165642 | GAAAAAAAGGCGGGG[C/G/T]GGGGAGTCAGGTAAG | 57630 |
| rs541566374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159184 | TCTGGTCATTCACAA[C/T]GCTGTGTACTCTGGT | 57630 |
| rs541608219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115809 | ATAAATCCATAAGTA[A/G]CACTTTTGATCAACA | 57630 |
| rs541610315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123414 | TTTTTTGCTAAAGCG[A/T]CTTTCAATAAAGATT | 57630 |
| rs541643768 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165646 | AAAAGGCGGGGGGGG[A/G]AGTCAGGTAAGGCCT | 57630 |
| rs541645750 | snp | A/G | 1.93737e-05 | 0.00311231 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269237 | CTTTACTGAGAAAAA[A/G]TCTTCAGAAATGTTC | 57630 |
| rs541650906 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101619 | CATGTATACTTTACC[A/G]CAATTTAAAAAATAA | 57630 |
| rs541673290 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094029 | CATACATGACCTCGT[A/G]CGACTCCACAAACTC | 57630 |
| rs541675655 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137368 | AATCTGTGCACTCCA[C/T]TGATATTATCAGCAA | 57630 |
| rs541682182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188401 | TCTCACTGTAAACAA[C/T]AGTGTCCACAAATCC | 57630 |
| rs541702618 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238999 | CTTTTTCAGTCTCAA[C/G]ATACCATGTCAGTCC | 57630 |
| rs541742038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172633 | GGTCAACTATTATGG[C/T]TCACATTAGGTGTCA | 57630 |
| rs541778667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152098 | AAATATACCCTTTTA[A/T]ACATATCATGGCATG | 57630 |
| rs541785970 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262118 | TCAAAAACTGGAGTA[A/G/T]GTCTATGTGCTTAAA | 57630 |
| rs541806482 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197898 | AAGACTCTGATCAAG[A/G]TAAAATACACAAAGT | 57630 |
| rs541809507 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095730 | AAAACTAAATATATT[A/C/T]CTAAATACATTTTGT | 57630 |
| rs541815698 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100990 | CTCCCCTGTGAAATC[G/T]CCAGCCCCATGGCTG | 57630 |
| rs541827737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224381 | GGAGTGCAATGGTGC[A/G]ATCTTGGCTCACTGC | 57630 |
| rs541839926 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166083 | AACCATAAGTTGACA[A/G]ATTTGACTGTATTGA | 57630 |
| rs541840727 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115346 | TGAGTGAGGCTTCAT[A/C]TGTATTTACAGCCGC | 57630 |
| rs541855459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231109 | GGTCGTAATACTTAC[C/T]TCATGGGGTTGTTGT | 57630 |
| rs541916976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237982 | AGAGTCCTATTAGGT[C/T]GGGTTAGCAAGAATC | 57630 |
| rs541939118 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258348 | CATTTCAAGCTGTCA[C/T]ACTTTGGGGCCTTTA | 57630 |
| rs541955597 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156954 | GGTGTTTTGCCTTCT[G/T]TCTTTGAGGTTATCA | 57630 |
| rs541976975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194138 | AGTGTATGAAGTTCA[C/G]GTAGTCGTCATCTAA | 57630 |
| rs541990556 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209931 | AGTAGCTGGGACTAC[A/G]GGCACGCATCACCAC | 57630 |
| rs542022847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159802 | TTCACATAGCAATTA[C/T]ATTTTTAATACATAT | 57630 |
| rs542069472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182439 | TCTTTTCAAAGCATT[C/G]TTAATTTCTTAATTG | 57630 |
| rs542113856 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140990 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTAAGC | 57630 |
| rs542116910 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266696 | ACTTGAACTCCTGGG[C/G]TCAAGTGATCCTCCG | 57630 |
| rs542121612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130490 | TCCAATGGACAGCCT[A/G]GTGCTCAACTAGCCT | 57630 |
| rs542147386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102242 | AGTCCAAGTAAATTA[C/T]GTCCATTGCTTCACC | 57630 |
| rs542148841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196703 | CAAGCAGACTTTTTT[A/G]TACTTTATCTTGCTT | 57630 |
| rs542150674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224784 | TAAGATGAGGGAGAT[C/T]TTGAAGACTGAGCCA | 57630 |
| rs542152887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189390 | GGGGCCAAGACTGGC[A/C]GAAGTCATGGTAGGT | 57630 |
| rs542177071 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167913 | AGGCCAAGGTGGTAG[C/G]ATATCTTGAGGCTGG | 57630 |
| rs542190181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145781 | TAAAATATTATATAT[C/T]CTATATATTATTCTA | 57630 |
| rs542197236 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146372 | GTAGCTGGTATTACA[C/G]GCGCATGCCACCACG | 57630 |
| rs542214097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240080 | GCACAAACACTCCAA[C/T]TGCACACTGGAACAT | 57630 |
| rs542214586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199123 | TTTAAAAGGGCAGCA[G/T]GTAAAGTAGGAGAGA | 57630 |
| rs542217978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248269 | ATAGACCGCATAAAG[A/G]AAATGTGGCACATAT | 57630 |
| rs542222677 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096277 | AAAAAAAGTTTCTCT[G/T]TGTAGTAAATCAGAC | 57630 |
| rs542251908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149737 | TTAAAGGAAAATAAT[A/C]CATCTAAAGGAAAAA | 57630 |
| rs542276001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099301 | ACTATATTGCCCAGG[C/T]TGGTCTTGAACTCCT | 57630 |
| rs542285210 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151530 | CACCAGTATGTGTTT[-/G]GGGTACAGCAAGTGA | 57630 |
| rs542308042 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162706 | TTTTGCCTTTATTCT[A/G]CTATCCCAGTGTCCC | 57630 |
| rs542317089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134714 | GATCCATGTCTTTTT[C/T]TCACACGGATATGAT | 57630 |
| rs542358336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132713 | AAAAAGGAGGTGGGG[A/G]TGGGGGTTTATTGCT | 57630 |
| rs542392001 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222724 | TAATCTTTCACCTTC[C/T]AAAATGCATTTTACA | 57630 |
| rs542414475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152168 | GCTTACACAAGTGAA[A/G]AAAGGGCCTGTCTAA | 57630 |
| rs542441407 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114376 | ATCCTTGAGTTTACA[A/C]TGGGCCCACCTGGAT | 57630 |
| rs542443963 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210320 | TTGAAAACTGAACTT[A/T]ACCTTCTAATTCACA | 57630 |
| rs542464030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155210 | AAACAGGAAATAGTG[C/T]AGGTGACTGACAATA | 57630 |
| rs542478869 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109252 | AAATTACAATCTCAG[A/C]AAGCCACAGCTAAAG | 57630 |
| rs542482048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181550 | ACAGGCGTGAGCCAC[C/T]GCGCCAGCCCTGGGA | 57630 |
| rs542484735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104589 | TAGAAAATTATTGTA[C/T]AGCACTATAAAAATA | 57630 |
| rs542492722 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201429 | ACACATAGGCACACA[A/T]GGGAATTATTTTACT | 57630 |
| rs542520386 | snp | A/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271493 | GGACCCTTCCTCCCC[A/C]GGCTGGGCGAGTCGC | 57630 |
| rs542525763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185355 | TGAATACTAGACATA[G/T]CAAGGAAAAGGGAAG | 57630 |
| rs542549299 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209421 | TCAGTTTAAGGTATC[A/G]TCCCCCGGGAACTCT | 57630 |
| rs542584386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114617 | CTTATCAGTGGCAAG[G/T]GCTCTGAGACACATT | 57630 |
| rs542596303 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250907 | AGCCATGTTGAGACC[C/T]GGGTAAAAGCTGACC | 57630 |
| rs542598172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242857 | CAATCTTGGACTTCC[C/T]AGCCTCCAGAACCAT | 57630 |
| rs542641025 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142131 | CCTTAATTTGCAATT[C/T]TTTTAGTAGAGATGG | 57630 |
| rs542653923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223567 | GTGGGGGATACACCA[C/T]GACACACCATGAATA | 57630 |
| rs542657857 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215106 | ATTTGGGGTAAATTT[A/T]TTTTCTTATCAAGTT | 57630 |
| rs542659534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250161 | TAAAAAAGCATTCCT[A/T]TCCATGCTCTCATTT | 57630 |
| rs542668518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206137 | CAGTGGTGCTAAAGA[C/G]CATCTCTTGCATATC | 57630 |
| rs542684807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256825 | TCAGGCTGGTCTCAA[A/G]CTCCTGGCCACAACT | 57630 |
| rs542704236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142938 | TGGATGACCTAAATA[A/T]AAAAGCAAGCTCAAA | 57630 |
| rs542724114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158090 | TGATGACTTAAAGAA[A/G]AATAAGACAGTTCTT | 57630 |
| rs542729879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214118 | TTGGAGGTGGGGCCT[C/T]GAGGGAAGTGTTTGG | 57630 |
| rs542738773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179036 | AGTAGACCACACCCC[A/T]ATCCCTGAACCCCAT | 57630 |
| rs542746240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264755 | TGACCCTTCACCCTA[C/T]GTGGCCCTTGGGGCA | 57630 |
| rs542758591 | snp | A/G | 4.97195e-05 | 0.00498571 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116356 | GAGTCCAGGGAGAAC[A/G]GTCACTATCCGGCCA | 57630 |
| rs542758979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230140 | AACCCAGGGGCGGAG[A/G]CTGCAGTGAGCCAAG | 57630 |
| rs542775084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229738 | CATCACAACTGGGAA[A/C]AAAACCAGCCCCACT | 57630 |
| rs542815712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186081 | TAGTAAGGAAAGAGT[A/G]TCACCTAGATGAAAG | 57630 |
| rs542836166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236376 | TGACTCTAATGACTA[C/T]AATGAGCGGTGTCCC | 57630 |
| rs542847113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201687 | ATACCATAATCATTT[C/T]CATGGTAACTTCCTG | 57630 |
| rs542847953 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252428 | AAATGTTTTCATGAC[C/T]ATTGAAAAGGGCTAT | 57630 |
| rs542876286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112949 | AATGAGTGAAGAGTT[C/G]GGATTTAGAGATCAA | 57630 |
| rs542877060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156213 | AAGATAATCTTTCAT[A/G]TAAGAAGTCTGTGCA | 57630 |
| rs542901961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129586 | CCACAGCTACAGACC[A/G]TATGGACACAAGACA | 57630 |
| rs542903886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105289 | TATTTATATAAGATA[C/T]AAAAAGAGTCCACTA | 57630 |
| rs542910364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208631 | GTGCCCCAAGGAGAA[A/G]AGGAGATGACACACA | 57630 |
| rs542925757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114046 | TTGGTCAATGGGGCA[C/T]GCACCTAGGCAGAAG | 57630 |
| rs542935274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243449 | ACCCAGCAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 57630 |
| rs542949297 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259557 | CCACGAAAAAGGGTG[C/G]CTGGGGCTCTGAATT | 57630 |
| rs542963680 | snp | A/G | 3.29679e-05 | 0.00405991 | missense | SH3RF1 | GRCh38.p7 | 4:169122133 | GGCCGTAAATGTGCA[A/G]TCTGGTCAGTGGATC | 57630 |
| rs542967271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258979 | TCCCACACTGACACT[C/T]TTACTTACATTGCTA | 57630 |
| rs542971477 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202086 | CAATGCTGTCAGCTT[-/A]AAAAAAAAAAATCTC | 57630 |
| rs542975762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266844 | TAAGTATTGCATCAA[C/T]TGCATCAACTCAGAC | 57630 |
| rs543000953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163960 | TGATTCTTGTGTGGG[A/T]CAATAGGACAGTCTC | 57630 |
| rs543013948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157532 | ATGATACTTTTCAAC[A/G]GCATTGGGGGTGCCC | 57630 |
| rs543050227 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135343 | AGGGGACATAATTTC[A/C]TTTTAATGTTTAAAG | 57630 |
| rs543052354 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177855 | ATGTGTATGTATATA[-/AT]ATATATATATATATG | 57630 |
| rs543064227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163522 | ACAGGAAACTAGAGA[A/G]GTAGGACGAAAACCA | 57630 |
| rs543081154 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173978 | CGGCTAATGCTAGTT[C/T]TTCAATTGTAATTTC | 57630 |
| rs543116737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145180 | AAGTCACGAAATCAA[A/C]CTGAGTGTCCATCAA | 57630 |
| rs543149709 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259778 | ATGTTGCTATGTAAA[C/T]GAGGCTTGCCTGCTA | 57630 |
| rs543151265 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178375 | AAATAAGCATTGTTA[A/T]GTTTTGAGGCACAGA | 57630 |
| rs543162855 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111973 | CTGTTCAAAGGAGTA[C/G]CCGGTTAGAAGAGAA | 57630 |
| rs543164707 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232575 | AGAGGTTAAAATAAA[A/G]TACAAACTTTGGTCA | 57630 |
| rs543184171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199324 | TTCAGTGGCTTAACA[C/T]ATCATTCTCATAACA | 57630 |
| rs543192773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128971 | TGAAGTAGATACTTA[C/T]TTTATGGCTAGGGTT | 57630 |
| rs543215070 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113735 | AATCATGGAATTACT[A/G]AATTTATATCAACCA | 57630 |
| rs543215717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156792 | AAACCACACTGTAAC[C/T]CTTGAAGAAAATCTC | 57630 |
| rs543228184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179224 | ACAGAGATGCAACTT[C/T]GCTGGCTTTGAAGAC | 57630 |
| rs543238900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193624 | CGGCTTATTGTAATG[G/T]CTGAGTAATTATTAC | 57630 |
| rs543251884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148748 | CTGTTTCATAGAATT[G/T]GTTTTGTTGCATACG | 57630 |
| rs543254037 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121582 | TGCCCACGAACACAT[A/G]GTAACCAGGCAGGCA | 57630 |
| rs543262515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200887 | CTTAATGGGTCAGAA[C/G]AGCTATGAGGTCCCT | 57630 |
| rs543288267 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098599 | GATCTGAAGCAAAAG[A/C]ACAGCACAGAAGTTG | 57630 |
| rs543290951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178465 | AGGACGAGGAAGTAC[A/C]TTCAATGCCCAAAAG | 57630 |
| rs543291029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186990 | CTGCACTCCAGCCTG[A/G]GGACAGAGCGAGGCT | 57630 |
| rs543326463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207939 | GGGTGTCAGTAGGGG[C/T]GGGGGGATCCTGCAC | 57630 |
| rs543330321 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233064 | GACCAGCCTGGCCAA[C/T]GTGGCAAAACCCCAT | 57630 |
| rs543334160 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121859 | AAGTTCAAACAGGAG[C/T]TGTACAAAAGAGGCA | 57630 |
| rs543351061 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131507 | CTGTGAACCAAAGTC[C/T]ATTTCCAACCTATTT | 57630 |
| rs543362070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229906 | TTACATGAGTGGGTC[C/T]TTTAAAAAACAATGC | 57630 |
| rs543401088 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116185 | CAGTGAGTCCTCTCA[C/T]TAGCTAAAAATGACA | 57630 |
| rs543403723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208899 | TCTCAAGATAGTTAC[C/T]GTGACTAAAAAAATA | 57630 |
| rs543413253 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169112 | ATGTGCATATTACTG[G/T]TACTGTTCTTCAAAG | 57630 |
| rs543416481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244357 | CCCCTCCACACAATG[A/G]ACCAGTGCTGATTCA | 57630 |
| rs543418100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236384 | ATGACTATAATGAGC[A/G]GTGTCCCTCTGCCAA | 57630 |
| rs543429594 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259283 | GCACTACGTAACTTA[A/G]AAATTCATTTGCACA | 57630 |
| rs543446359 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100927 | GTCTCCTTTGACGCT[A/C]TCTCTCCCACCCATA | 57630 |
| rs543476290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164704 | ACTAAAACATAGTCC[A/G]TTCTGGAAGTGGGCA | 57630 |
| rs543500001 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250950 | AGGGCAAAGACTAAG[C/T]GCAAAGGCCCTAGGC | 57630 |
| rs543507941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101548 | TGAATGGTTGTATGA[C/T]AACATGAATGTACTC | 57630 |
| rs543539195 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171923 | TGCTTCTTCTCCATC[C/T]GCACTGCAGTGAATC | 57630 |
| rs543555227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171199 | ACGGTGTAACCAATC[A/T]GGTTGTTTCTGTACC | 57630 |
| rs543560436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129712 | GTATTTTCATAAATG[C/T]GTCCTTATAAGAAAT | 57630 |
| rs543569288 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105277 | ACAAATACTATATAT[G/T]TATATAAGATATAAA | 57630 |
| rs543572755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207091 | AGCCTCCCAAATAGC[A/G]GGGCTACAAGTGGGT | 57630 |
| rs543578683 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180647 | ATTGGTTTGGTCTTT[A/G]GTTGTTGCCTACTTA | 57630 |
| rs543600826 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144348 | GTACAATACCTATTC[C/T]CAACCCAAACAAAAA | 57630 |
| rs543607217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105347 | TATGTAATGAATAGT[G/T]CCTCATTGTTGAGTT | 57630 |
| rs543614729 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110790 | ATGGATCTAGGATAT[A/G]GCAGAGTGCATGTTG | 57630 |
| rs543631985 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108382 | CTAAATCCCTAACAA[C/T]ATTGTTCCATTAGAG | 57630 |
| rs543640657 | in-del | -/ATG | 0.00255881 | 0.0356771 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107240 | AGCCTTAGTTGGAGA[-/ATG]ACAGTACTATTGCTG | 57630 |
| rs543650706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230227 | AAATAAAAAACAATG[C/T]TTAATTCAATATGAC | 57630 |
| rs543662577 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199156 | CAACTGGAGTTGTAT[C/T]TGAAGATCCTCATGG | 57630 |
| rs543667092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149786 | ATGATGCTATCTTTT[C/T]ATATAGTTCAATCAA | 57630 |
| rs543668151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105934 | TTCTCTAATTCAAGC[C/T]TGTCCAACCCGTGGG | 57630 |
| rs543690316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246515 | CTACGTGCCTAAAGG[A/G]GAAAGTAGAAAAAGA | 57630 |
| rs543726133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202195 | TTTATTAAGGGCCTA[C/T]TTCGTGTTCTTGGTG | 57630 |
| rs543738918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099374 | GATTATAGACATAAG[C/T]CGCTATGCCCAGCTC | 57630 |
| rs543751195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236947 | AAGTAGAAGAGAGAC[C/G]ATTGTATTTAACTGA | 57630 |
| rs543755489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253196 | ACCTAGAAACCACAG[A/C]GTGGCACATTTCTAA | 57630 |
| rs543759952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252506 | TTGTAATCTAATTAC[C/T]CCCTACCATCTGGCA | 57630 |
| rs543761582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115586 | GGCTCCCACTAATTC[G/T]ACATTATGGTGAGTT | 57630 |
| rs543776229 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228457 | TCCAGAGGCTGCCTG[C/T]ATCACTTGCCTTGGG | 57630 |
| rs543839448 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151227 | ATTCTAATGGGGAAA[C/T]GGAGGGTGAGGGGTC | 57630 |
| rs543860489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220442 | CTGTTTGATCCTCTC[C/T]TCCACAGGATAAATT | 57630 |
| rs543864105 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124963 | CCAGGCCAGCCCAGG[C/T]ACCAGAGGCCAAGTA | 57630 |
| rs543866671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154370 | TCTCTATGGAGGAAA[C/T]TGAGTGCTGGCTACA | 57630 |
| rs543887281 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164018 | TGTCCATCAGGACCC[A/T]GCCCAGGCATTGCCT | 57630 |
| rs543892353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104408 | ATACAGCAGGAAAAA[C/G]GTTGACTCTTAGAGT | 57630 |
| rs543896466 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094192 | AGGTCAAATGTGTCC[C/T]GTGTTTTTTGTTTTG | 57630 |
| rs543913943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259161 | TGAATTGATAAGCAG[C/T]TTTTTCTGGCAAAAA | 57630 |
| rs543916201 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267286 | CAACAACTAAGATAC[A/G]GTATTCCAGGAAGCC | 57630 |
| rs543921077 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184743 | TTTATTTTTTGCACA[C/G]TGGCTAAGAATAGAA | 57630 |
| rs543921881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219967 | CTTCCAGGCGATCAG[C/T]ACAAACTAGCGTGTG | 57630 |
| rs543927965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140890 | CACTAGAGCAAGCTT[A/G]TCCAACCCACGGTCC | 57630 |
| rs543972553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242049 | TATATGTCAAAGAAT[A/G]CTATAAATAGGATCC | 57630 |
| rs543998208 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188200 | CAAAGTTTTTGGTAA[A/T]TTGTTACAGCACCCC | 57630 |
| rs544017188 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124697 | ATGTTGCTTGCCCCT[C/G]TGGGGTTGGTGAAAT | 57630 |
| rs544018320 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182292 | TGACTTTTATATGCG[-/A]AATCAGGTAAAATAC | 57630 |
| rs544023831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174790 | AAATCTCTGGGGCTG[A/G]GTCAGAAGCATACGG | 57630 |
| rs544035712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114724 | AGTGCAAGTTTAATG[C/T]AGTTAATTATAAACA | 57630 |
| rs544039175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241290 | AGTCCATGTGAAAAG[C/T]ATCCAAGTTTACACA | 57630 |
| rs544054927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125487 | GAGGGGAAGTAGTCC[A/G]GTACGTCTCAAACTT | 57630 |
| rs544059725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185665 | CTACAGTCACAGCCA[C/T]AAGCCTGAGGAGGTT | 57630 |
| rs544092560 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245790 | AGTGAAATGTAATTT[G/T]TAAGTAATTTTTAAT | 57630 |
| rs544095640 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248920 | TGTGATGGTATTAAG[A/T]AGTAGGGCCTTTAAG | 57630 |
| rs544097186 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094818 | AGGAATGATTTCATC[C/T]TCAACCACATAAAGT | 57630 |
| rs544102199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110143 | ACTTTGGGAGGCCAA[C/G]GCGGCAGGATTGCTT | 57630 |
| rs544103151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157654 | ATGTCTATAATAATT[C/T]CCTGAACAAGATTAC | 57630 |
| rs544145114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197670 | ATTGTGTTTGTTGTT[A/G]TATGTCTTATAAAAC | 57630 |
| rs544165909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158259 | TGACACATGAGCCAA[A/G]TCTTAAAGGATGCAC | 57630 |
| rs544181235 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243468 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA | 57630 |
| rs544188203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161498 | TGGCAAAATGCTACT[C/T]GATGAACTAGCTGAG | 57630 |
| rs544188400 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270697 | GCGGGCTGCTCCGCT[C/T]CCGCAGGTCCTGATT | 57630 |
| rs544202014 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246878 | TAAATATGACAATCT[G/T]GCAAGACTGCTGTAG | 57630 |
| rs544209507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204333 | TTCATTCAATCATCC[C/T]ATTCTCTGTCAAAGG | 57630 |
| rs544246173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262961 | TAAAATAAGAGGTCA[A/T]GCATGCAACAAACAT | 57630 |
| rs544248369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167880 | CTCAATACCAAAGGA[C/T]ATTAAGGTAACACTG | 57630 |
| rs544271340 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212125 | GCTGGAGTGCAATGG[C/T]ACGATATCAGCTCAC | 57630 |
| rs544279740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262270 | AAGATCTGCAAGTAT[A/G]TACACACTTAATAAC | 57630 |
| rs544281877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175239 | CCAGATCAACACCAT[C/T]TGTATTGCCACTATT | 57630 |
| rs544307283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234880 | CATGGTAGGACGCAC[A/G]GCATTTCTGGCTTCT | 57630 |
| rs544308911 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270820 | AGGGGTCCGCCGACG[A/C]TGGGTCCCCGTCGAC | 57630 |
| rs544310801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167194 | TGAATACACATCTTG[A/G]AAAGAAGATGTTTGT | 57630 |
| rs544324195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148211 | ATGCTAGTTATTGAA[C/T]GTGCTCTGAGACTAG | 57630 |
| rs544338102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156257 | CTTGTGACTTAAAGA[C/T]TGCTTCTAGGCATTT | 57630 |
| rs544431872 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249347 | TAGCTTGCCCATAGA[A/G]GGCCATGTGAGGACA | 57630 |
| rs544437432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250337 | AAAAAAAAAGCTTGC[A/G]GCAAGATTATTTTTT | 57630 |
| rs544452268 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204937 | TTAAGAAGCTGCTTG[C/G]TGATTTTTAAAAAGG | 57630 |
| rs544485700 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264759 | CCTTCACCCTACGTG[G/T]CCCTTGGGGCAGTTC | 57630 |
| rs544494786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256156 | AAGTCTTTAGTAATA[C/T]GCTAAAGAAATAACT | 57630 |
| rs544590699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127239 | AATGTTTATAACTTC[A/G]TTCTGCATAAAAGAT | 57630 |
| rs544609176 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152036 | TGTTTTTGAACAAAG[A/C]AGCAGATTAAAAATC | 57630 |
| rs544627264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169069 | GCCTTTTATCTTCTT[A/C]TTTTTGCTGTTGAGA | 57630 |
| rs544628340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185194 | ATGCCAAGCACTGTG[A/C]TAAACATTGAGGATA | 57630 |
| rs544631905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120668 | TTTTAGAGTTAGAAG[G/T]GATTTTAGCAGATGT | 57630 |
| rs544649615 | in-del | -/CT | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099287 | AGGGATGGCATCTCA[-/CT]ATATTGCCCAGGCTG | 57630 |
| rs544655442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204518 | CAGAAATTACACTAA[C/T]TCTTACCTGGTTATC | 57630 |
| rs544672906 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263578 | TTTCTCCCACTACTT[C/T]CTTCAATTCTTTCTG | 57630 |
| rs544700180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098398 | TACAACTGTCCCCAA[A/G]CTTCTGAAACCTATT | 57630 |
| rs544720440 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113117 | CCCAGTTTTCTTTTT[C/T]TTTTCCCCCCTGAGA | 57630 |
| rs544741418 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118984 | ATTTAAATGATAACA[A/G]TTCTGTATATAGTAA | 57630 |
| rs544748516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257735 | GCAGTGTAACAACTT[C/T]AGATGAAGATAATAA | 57630 |
| rs544763869 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150380 | ATTGACAAAATTGTA[-/T]TATCTTTATCATGTA | 57630 |
| rs544770739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235804 | TCAAGCCTCAGCCTC[A/C]TGAGTAGCTGGGATT | 57630 |
| rs544795122 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122900 | CAGTGAAAAGCTGCT[A/G]GTTCCTTTATGGGCA | 57630 |
| rs544811801 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214818 | GTATCCTTCAACCTT[G/T]CTAATTGACTAATAA | 57630 |
| rs544876593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169426 | ACATGGCAAAACCCT[A/G]TCTCTACTAAAAATT | 57630 |
| rs544910243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103917 | CTATCAAAGAATTCC[A/G]GCATGCCCAGGCCCA | 57630 |
| rs544929841 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242607 | GTCACCCAAAATTCA[C/T]GTATTGGAAACTTAA | 57630 |
| rs544930909 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142451 | AAATAAGAAACCTAC[A/C]TTTTTTCCTACTTTT | 57630 |
| rs544936471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176851 | GGCCAATTTATATAG[C/T]TCCTTGATTAAAACC | 57630 |
| rs544962597 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212741 | TTATATCAGGGTTCC[C/G]TCTTGGTGTTCTATG | 57630 |
| rs544971988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121416 | GAAGCACAACACGCT[A/G]GCTTCTACACACAAG | 57630 |
| rs545016072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162017 | AAAACTCATCTCTAT[A/G]AAAAGTACAAAAATT | 57630 |
| rs545022179 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148286 | CCACGATTCCTTTCT[C/T]GATTCCTGGCTCTGT | 57630 |
| rs545026286 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228915 | GTAATGTTAGAATTT[C/T]ACTTTAAAAAAACAA | 57630 |
| rs545038856 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229691 | GCATATCTCCACAGA[A/G/T]TATTACTCATGAGTA | 57630 |
| rs545040080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213247 | TAGGTACCTGGTGGT[A/G]GCTCACTTTAATCTG | 57630 |
| rs545041568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256191 | TGAATTTTTTTAAAA[C/T]TACTTGAGCTATTAT | 57630 |
| rs545061646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214181 | GTACTGTCCTTGCAA[C/T]AATGAGTGAGCTCTC | 57630 |
| rs545075496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264941 | CTTCCCTGCCCAGCC[C/T]CCATTCCCTAATTAA | 57630 |
| rs545077874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168827 | AAAAGTTTATTCTTG[A/G]TGATTTTGTCCTTTG | 57630 |
| rs545085938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148654 | CTAATTATACACTTA[C/G]CATGTTCCAGGCAAG | 57630 |
| rs545099673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228806 | CAGACATATACCACA[A/C]CCATACCCAAAAGTT | 57630 |
| rs545103877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263814 | AGTTTTCCCCTCTCA[A/G]TATTTCCTTCATTTC | 57630 |
| rs545110742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222293 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57630 |
| rs545111502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221141 | TTCTGTGCTCTCTAG[C/T]GAGCAAGAGTAATCC | 57630 |
| rs545134117 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149836 | AAGGTTATTATTGTG[A/C]CCTTCTGCTATCATT | 57630 |
| rs545215863 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251093 | TGGACCATTATATAA[A/C]ATAGTTTTGAGCAAG | 57630 |
| rs545216604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182637 | TTATAAAAGGCTTAC[A/G]GGAAATATGGCTGGT | 57630 |
| rs545221287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243773 | TTTCCCTATTTGAAC[G/T]TTTTAGAATCAGAAT | 57630 |
| rs545249463 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163628 | GGAGACAGTTCCCAA[C/T]TACCTCTTAAATCAC | 57630 |
| rs545293244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111697 | AACTGAATATGAAGT[C/T]AGCAGTATGTCCAGA | 57630 |
| rs545300709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163882 | CTTGGATTTTTATGT[A/C]TGTCTAGGATGACTG | 57630 |
| rs545311445 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207478 | ATTTCTGGATATTAT[A/G]CCATTTGCTAAACCA | 57630 |
| rs545323954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135112 | GGCCCAGGTAGGATG[C/T]TCACTTGAGGCCAAG | 57630 |
| rs545357819 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155178 | TTTCTACTCCCACCA[A/G]AGCCAGCAAATGGAA | 57630 |
| rs545375746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124521 | AAAGGTTCTTCCTGA[C/T]AGAAAAGAGTTCTCT | 57630 |
| rs545389054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119485 | TGTTTGACAAAAAAA[A/T]TTTTATAAAAATGTT | 57630 |
| rs545401305 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268405 | GCTTGATTTCCTATT[A/T]ATGATTTACCCACAC | 57630 |
| rs545404307 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175128 | ATTCTTTCACATTGC[A/G]CATCCACTTAATGCA | 57630 |
| rs545410465 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206262 | CTTAGCATGCCACAC[A/G]TGATTCAATCTAAAA | 57630 |
| rs545427615 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113880 | AGAAAAGACACAAGG[A/G]GACACACCTGCAAAT | 57630 |
| rs545428429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173827 | ACCTTGGTTATGAAA[A/T]CTTCATTAATCAGAG | 57630 |
| rs545442345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232161 | CGCTAGTAAGCACCT[A/G]TGAGGCAAGAAAGGA | 57630 |
| rs545457154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156885 | ACATAAGAACAGTAC[A/G]ACACCCATGCACCAG | 57630 |
| rs545489595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106056 | TAGTGTGTATATATA[C/T]GTAATGTAAAATATT | 57630 |
| rs545499752 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266711 | CTCAAGTGATCCTCC[A/G]GCCCCAGCCTCTGGA | 57630 |
| rs545506592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231672 | CTCAAAGCTGCTATA[A/G]AATACTCACTCCTCC | 57630 |
| rs545522460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117189 | ATGATCAGCACACCC[A/G]TTAGTAGAGTATCAC | 57630 |
| rs545569104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134656 | TCTTTAGTTCTGAAC[A/C]TTTCTGGATTAACCT | 57630 |
| rs545607286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207836 | GAGACAGTTGTTTAT[A/C]CAGGTGCCACTTTCT | 57630 |
| rs545637055 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163238 | TATTCAAACACCCAG[-/A]AAAAAAAAAAAATGA | 57630 |
| rs545639188 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094987 | GGATCTTATTCATTA[C/T]CAGGCTGTCTTCCCT | 57630 |
| rs545647729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131279 | ATCTGTATCTATTAG[C/T]CTATATATTGATTGA | 57630 |
| rs545648617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178523 | AGACTTGGGCCCAGA[C/T]CTGGGTGGACAGGGC | 57630 |
| rs545669694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138243 | TATTATAGTGGGAGT[A/G]GCCTGAACCTCACTG | 57630 |
| rs545672528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261411 | TGCTAAAAGCAACAT[G/T]AGGTCCCAGGGAAAA | 57630 |
| rs545708924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123667 | GAGGCTGAGGCGGGC[A/G]GATCACGAGGTCAGG | 57630 |
| rs545732729 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097560 | ACAGCTTGTAGGAAA[C/T]GAGAGGGAGGTGACT | 57630 |
| rs545733844 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269330 | CATGGGGAAAAGGGG[A/G]AAAAGAGAACATGAG | 57630 |
| rs545744317 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209423 | AGTTTAAGGTATCGT[C/T]CCCCGGGAACTCTCC | 57630 |
| rs545756276 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144778 | TTTTTTTTTTAAGGA[A/T]AGCTTATGTAAAACC | 57630 |
| rs545768058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166301 | ATTGAGAAGCTGGAT[A/G]CTAAAGAGAAGGAAC | 57630 |
| rs545799850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172787 | ATTGGCTGCCAGCGC[A/G]GCTAGAACAAAGCAA | 57630 |
| rs545803590 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224506 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 57630 |
| rs545807811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191463 | TTGTGAAAATGACCA[C/T]ACAGCCAAAAGCAAT | 57630 |
| rs545816605 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183453 | CCCAGCTAATTTTTG[-/T]TATTTTTAGTAGAGA | 57630 |
| rs545832785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224930 | AGCCTAAGGGACATC[A/G]AGTCTCATTCTGTAA | 57630 |
| rs545858604 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187399 | GGTCTCTATATTACC[C/G]AAGCTAGTCTCAAAC | 57630 |
| rs545878185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190322 | AAATTGATAGACCAT[C/T]AGCAAGATTAACAAA | 57630 |
| rs545941459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196935 | TTAGTTTTGCCTATT[C/T]AAAAAATAATGAATA | 57630 |
| rs545952938 | in-del | -/C | 0.0310518 | 0.120672 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113121 | TTTTCTTTTTTTTTT[-/C]CCCCCCTGAGACAGA | 57630 |
| rs545972203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248379 | ATTCTCAGCAAACTA[A/T]CACAGGAACAGAAAA | 57630 |
| rs545986201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153252 | ATAGTGGTGTCAGAC[C/G]CTTGGAGATACATCA | 57630 |
| rs545995571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254223 | CTATCAGTTCCATCA[A/G]GAAGTATTTACTGAA | 57630 |
| rs546000451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175302 | CTGTTAACCTCAGAA[C/T]GGCTTTCCCTCCCAC | 57630 |
| rs546009415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203071 | GCAAAGAAACCTGTT[C/T]ATTGTTAAGAAAATG | 57630 |
| rs546065595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174849 | TATGAAGCGCTAAGA[A/G]CTGTGGATCTACACA | 57630 |
| rs546068634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220617 | CCTGCCCCACTTCCA[G/T]CAGTCTGGGCACCTG | 57630 |
| rs546085003 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169270940 | GCCCCACCGCGCTCG[C/G]CGCTCGCAGTGTCTC | 57630 |
| rs546126977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182695 | TCTTCCCTCTCTTCA[C/T]AGCAGGCTTTATTGC | 57630 |
| rs546140622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146450 | GGTCAGGCTGGTCTC[A/G]AACTCCTGAACTTGT | 57630 |
| rs546148041 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138606 | TCTTCTCATTGAGGC[-/A]AAAAAATATGAATAG | 57630 |
| rs546169498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140635 | AAAAACAACAAGGCA[A/G]CTTAAGAAATATTAA | 57630 |
| rs546193459 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261805 | CCTAGAGATTAGGAA[A/C]AAAGGAGTAGAGATA | 57630 |
| rs546210774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132848 | AAAACATCTTGGCTG[C/T]TTGTACCACCATGTG | 57630 |
| rs546217724 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129983 | TGTTAGGAGGTGGAG[C/T]GTGCCAGATTAACAT | 57630 |
| rs546244167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101923 | AAGCTCCACAGACTT[C/T]CAATGCTATGGTATT | 57630 |
| rs546274170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125546 | GTAAAGTGCTTTGCA[C/T]TGGAGCTTTGGACAC | 57630 |
| rs546303853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196142 | ATAAAGTCTATTTCT[A/G]TAATGCCAATCTATG | 57630 |
| rs546306860 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100584 | TGACCTGGTGATCCA[C/T]CCACCTTGGCCTCCT | 57630 |
| rs546344789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109941 | TTGCTTGAGCCTGGA[A/G]GTTGAAGTTGCAGTG | 57630 |
| rs546345950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203423 | AGGCACGGTGGTGTG[C/T]GCCTGTAATCCCAGC | 57630 |
| rs546373983 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116096 | ATGGGGTGGTGCCTG[A/C]GTTTCTTCCCCACTC | 57630 |
| rs546376030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123834 | GAGGCGGAGCTTGCA[G/T]TGAGCCAAGATTGCG | 57630 |
| rs546432161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232873 | ACCCTAAACTCTGAA[C/T]ATATAATCTACTAGT | 57630 |
| rs546437520 | snp | C/G/T | 3.70887e-05 | 0.00430619 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169116631 | GGTTGTGCGCTGCAA[C/G/T]TAGTAGATGGGAAGA | 57630 |
| rs546452316 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095833 | TAAATTGAGGACTAG[A/G]TCTTCAGGGTGATTC | 57630 |
| rs546467838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247921 | ATCATTAGAGAAATG[C/G]AAATCAAAGCCACAA | 57630 |
| rs546468428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227157 | GGTGACAGAGCAACA[C/T]CCTGCCTTGAAAAAA | 57630 |
| rs546472886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189681 | TGGGACCAGGCAGGC[A/G]TGGGCTCCTATTTCT | 57630 |
| rs546487844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226384 | AGTTGTCGTGTCTAC[A/G]TATCAAGGTTTTCCT | 57630 |
| rs546515477 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096321 | CCTTATACATCCGAA[C/T]CCAGACTAACAAAAC | 57630 |
| rs546529269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254343 | GTACAGGAGACAACA[C/T]TAAAGCACAATTAAT | 57630 |
| rs546547057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109394 | AAATGATTAAACACA[C/T]TAAATACAGCTTGCT | 57630 |
| rs546574880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215272 | ATTGATTTTTCAATA[A/C]TGAACCAGCCTTGCA | 57630 |
| rs546587693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108803 | GTGGCAGTGCTGTAT[A/C]TACCTCTCTATCTCA | 57630 |
| rs546598722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174967 | GCATCCACAAATCAA[C/T]GTGTCCAAAACAGAC | 57630 |
| rs546601530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202558 | CTAGCTTATAATTAG[C/T]ATTTGGGTTAATAAC | 57630 |
| rs546660119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174279 | GTTGCCTAGGCTGCT[C/T]TCAAATTCTTAAGAC | 57630 |
| rs546687716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270398 | GTGGGGATCTCACCC[C/T]ACAGCCTCCCTCATC | 57630 |
| rs546694067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161074 | GCCAAGGCCCCCAAG[A/G]ATCCACAGAGCTTAC | 57630 |
| rs546699657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165756 | AAACATAAGGTTAAA[C/T]GTAAAAGATAGTTCA | 57630 |
| rs546735754 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241759 | TGACCTTGCAGCATG[G/T]TTACTGAGATACTGC | 57630 |
| rs546757159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153867 | CAACTTAAGTCAGAG[C/T]AAATAATCCTGATGA | 57630 |
| rs546775344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187252 | CACCCAGGCTAGAGC[G/T]CAGTGGTGTAATCTT | 57630 |
| rs546786313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140197 | TCAGGCAGAAACATA[A/C]AGCAGCTTTTGCTGT | 57630 |
| rs546791341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158730 | GCATTACTTATATCA[C/T]TGTCTGCCCCCCGAC | 57630 |
| rs546836244 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161658 | AGTAAAAAAGATTCA[A/G]TGACCTCCTAAAAAG | 57630 |
| rs546869144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239477 | TAGTCACTGTTATTC[A/C]GTCCATATGTATGTA | 57630 |
| rs546871944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168097 | ATGAGCTATGATTGT[A/G]TCACTGCAGTCCAGC | 57630 |
| rs546875827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132223 | ACCAAAATACAACTT[C/T]CTGGGCCTGACCCTA | 57630 |
| rs546878750 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196264 | TCACTTAACATCATC[A/C]ACAGGTTCTTGGAAA | 57630 |
| rs546935449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167521 | CACTATTTATAATAC[A/C]AAACACTGAAAACAA | 57630 |
| rs546935956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195460 | CTTGAGTTTGTAAAT[A/G]GAAGTTATTTATCAG | 57630 |
| rs546940070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203158 | AACATGCTGTTATTT[A/G]GTAAGCCACACATTC | 57630 |
| rs546949272 | in-del | -/G | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228948 | AAAATTCTGTTCTTC[-/G]AAAAACAAACAAACA | 57630 |
| rs546983194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220026 | AGAGAAAAAAAGAAA[A/T]GAGAAAGCAGAAATG | 57630 |
| rs546985876 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212292 | TGGTCTTAATCTCCC[A/G]ACCTCAGGTGATCTG | 57630 |
| rs547041686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182750 | GTTCAAGTGTAAAGA[A/G]CGATACACTGACTAT | 57630 |
| rs547046984 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219267 | ACCCTAAATCATCAG[A/G]AGAGGGTTAATTTAT | 57630 |
| rs547062213 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233381 | ATCATAAAATAATTA[A/C]CAAATTTCAAAGAAT | 57630 |
| rs547106496 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222762 | CTGAGAAAGAACTTA[C/T]GTTAACAACTCTCTA | 57630 |
| rs547107414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190532 | TCAGGAAGAATTAGA[C/T]ACCCTGAACAGACAA | 57630 |
| rs547156127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204672 | TCACCTACCTCAGCC[C/T]CCTGAGTAGCTGGGA | 57630 |
| rs547161333 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142736 | AGTCACTTTGAAGAA[G/T]ATCAGGGAATGAATG | 57630 |
| rs547164110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236438 | GAGAAATAAGCCTTT[C/G]CTGTATTAAGCATCT | 57630 |
| rs547175433 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249023 | ACGAGGTCAGGAGAT[C/G]GAGACCATTCTGGCT | 57630 |
| rs547175803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200310 | CAAAACCTGTTTATA[C/T]GTTAAGCCACAAAAC | 57630 |
| rs547219844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157870 | TTCAGCCTCCCAAGT[A/T]GCTGGGATTGCAGGC | 57630 |
| rs547233362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132907 | AGACACTCATGAACA[G/T]CTATCTGATCTGGCG | 57630 |
| rs547237154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207600 | AAGACTAGAATTCTG[C/T]CCATAGTATGTGGTC | 57630 |
| rs547238591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248658 | TTCAAGTAAAATTTT[A/T]AAAAATTCAAAAAAA | 57630 |
| rs547259877 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263102 | TGCTTGGGTCCGGTA[A/T]GAGTTAATACACATC | 57630 |
| rs547294312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125687 | TTCTGGGTCCCTTGG[A/G]CAAATATTATTAATA | 57630 |
| rs547318651 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271021 | CGCACACACACCACG[A/C]CGCCGCCGCCGCCTC | 57630 |
| rs547322557 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216190 | ATATTACTATTGAAT[A/C]TTTAGAAGTCCATAT | 57630 |
| rs547329971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170599 | GAGCTATGTGAGGGC[A/G]GGGCTGGAGCTCATT | 57630 |
| rs547336905 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266550 | TGTATGGCCCTGACT[G/T]TTCTGAATATTTGAA | 57630 |
| rs547366672 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250688 | CTATTGTGGGGTAGT[A/G]GGGATGGGGGTAGGA | 57630 |
| rs547380184 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256014 | CTCAAGCAATCCTTC[C/T]GCCTGAGCCATCCAA | 57630 |
| rs547414450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114293 | CTCATTTCCCTATCA[C/T]TCCTACCTCTGCTTC | 57630 |
| rs547443300 | snp | C/T | 0.208169 | 0.246476 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229939 | GGCCAGGCGAGGTGG[C/T]TCATGCCTGTAATCC | 57630 |
| rs547461599 | snp | C/G/T | 0.000503882 | 0.0158649 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122201 | AGCGGCGGTGGCGCC[C/G/T]GGTGGTGTGGAGGCA | 57630 |
| rs547470108 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137931 | CTTTATCAAACATGA[C/T]CATATCTCTTCTTCA | 57630 |
| rs547477396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106311 | ACAGGGTTTTACCAT[A/G]TTGCTGGGATTACAG | 57630 |
| rs547477929 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139804 | TAGCACAGCCATTAC[C/G]TAACTTTGGGGCCTT | 57630 |
| rs547503692 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185484 | TACTCACAGGGAGCA[A/T]TATTCTTTTCTTTTA | 57630 |
| rs547510696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201100 | ACTGGCAATTTGAAA[A/G]AAACCTTTTCTATGA | 57630 |
| rs547551652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099856 | TCTGGGGGGGCGGGT[A/G]GAATGAGAAACTATG | 57630 |
| rs547551715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224946 | AGTCTCATTCTGTAA[A/C]AGGGTGCCCAAGGGT | 57630 |
| rs547555297 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211708 | AATTAAAGCCTAGAT[-/AC]ACAGATGTGTGAATG | 57630 |
| rs547559592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150424 | TAAAATATGTATACA[C/T]TGTGGAATGGCTAAA | 57630 |
| rs547564391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134833 | CATGTCTTATGTCTG[C/T]CACTTAGAATATAAT | 57630 |
| rs547611733 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260888 | ACTTTATAATCTTTT[C/T]GGTATCTTTTCAGTA | 57630 |
| rs547615698 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123748 | TACAAAAAAATTAGC[C/T]GGGTGTGATGGCGGG | 57630 |
| rs547631456 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151200 | CTGCGGAACCGGCCC[C/T]TGGGAGTTTGAATTC | 57630 |
| rs547650111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163644 | TACCTCTTAAATCAC[A/G]TTAATGGTCTAAATC | 57630 |
| rs547663726 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163854 | GCCTGATAATTATGC[C/T]GCATTTCTTTCACTT | 57630 |
| rs547675037 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231363 | ACGAGGTCAGGAGTT[C/G/T]GAGACCAGCCTGACC | 57630 |
| rs547677390 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128630 | ATCAAGACAAAATAA[A/T]TAACAAATAGGAAAA | 57630 |
| rs547679962 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215398 | GTTCATGACAGATAT[A/T]GCAGTTCCTTTTCTT | 57630 |
| rs547696448 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265621 | TGGGGTTATAGGCAC[G/T]TGCCACCACACCCGG | 57630 |
| rs547699883 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223083 | ATCAGTCCTCCAACA[C/T]GCAGACTCACTTTAA | 57630 |
| rs547787148 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237368 | ATTTCAGGCTGGACA[C/T]GATGGCTCATGCCTG | 57630 |
| rs547792336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266746 | CTAGGACTGAAGATG[C/T]AAGTAGCTAGGGGCT | 57630 |
| rs547819820 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133398 | GAGAATTGCTTGAAC[C/G]TGGGAGGCGAAGGTT | 57630 |
| rs547831752 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193791 | AGAAGTTAACACTCA[A/C/G]TGATGAAAACAGATA | 57630 |
| rs547843272 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102110 | AGGCACTCAGTTCAT[C/T]ACTCTGACCTGGGTG | 57630 |
| rs547858954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158571 | GACTTAGGTCCTATG[C/T]GCCGGACAGATCAGT | 57630 |
| rs547873509 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134888 | CCTTCACTGCACTCA[A/T]GTTCTAGTTGTGCGT | 57630 |
| rs547886124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171531 | GTAGAATATGACTTA[C/T]TGATAGTAATATAGG | 57630 |
| rs547894568 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131341 | GTGGCACTAAAAAGA[C/G]TTTCTCCCCAAACCC | 57630 |
| rs547952329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179341 | GTAACATAGCCCTGC[C/T]TACACCTTGATTTTG | 57630 |
| rs547960846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194210 | TTAGGCTTTTTGTAC[C/T]ATAAAATAAAGCATA | 57630 |
| rs547978267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180839 | CACTTATTCTTTAGG[C/T]TTTTTAACTCTAACA | 57630 |
| rs547986368 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230608 | TCACACCTGTATTCC[C/G]ATCACTTTGGGAGGC | 57630 |
| rs548018110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172164 | AGAGCTGAAAACATA[C/T]TATTGAAGGCTTGGG | 57630 |
| rs548019005 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151518 | CTCCCACTATGGCAC[C/T]AGTATGTGTTTGGGG | 57630 |
| rs548075858 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201913 | GGTCCAAACTGCAAG[C/G]ACCTGTACCAGGAGT | 57630 |
| rs548080770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151371 | TTGCTCTTGCTGGTA[C/G]CAGGCACTATTCTTA | 57630 |
| rs548085860 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171260 | TTTCGGTCCATGAAT[A/C]CTCTCTGACCACACA | 57630 |
| rs548126281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164281 | TAAATTAATGAAAGA[A/G]CAAAAGTTATCTCTA | 57630 |
| rs548136815 | snp | A/C | 1.83893e-05 | 0.00303221 | splice-donor-variant | SH3RF1 | GRCh38.p7 | 4:169130045 | GAGAAACTATACTCA[A/C]TCCAAGGGCAGCTTG | 57630 |
| rs548176012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188493 | AAGGCCCTGTATACA[A/G]CTTGTTACTCTAATA | 57630 |
| rs548183509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115168 | AGACATTAAAAAAAA[A/C]CCCAAAAACTATGGA | 57630 |
| rs548198200 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105569 | AACTGAGACTGAGAA[C/T]TTAGCCATACCCTTC | 57630 |
| rs548203630 | snp | C/T | 2.32021e-05 | 0.00340595 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122231 | AAGGACAGTGGCAGC[C/T]AGGAGAGGGGGTGGT | 57630 |
| rs548227010 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132137 | TCTTTGTTCAAAACG[C/T]GAAGTACATGGACAC | 57630 |
| rs548233848 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120136 | TAGCACCCCTAACCT[-/C]TAGTCGTGACAATCA | 57630 |
| rs548245675 | snp | A/C/G | 8.44893e-05 | 0.0064991 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107149 | TGGAGGAGACACGCG[A/C/G]GGCTTCCGTTTAGTG | 57630 |
| rs548245792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115864 | ATTTTTAACAGAACT[C/T]TTATCAAGCAAGACT | 57630 |
| rs548266204 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163620 | TACAATCTGGAGACA[A/G]TTCCCAATTACCTCT | 57630 |
| rs548297380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194341 | TAGAAGTGTGCCTTA[C/T]GACCTTACTAGTAAC | 57630 |
| rs548306114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107772 | TGATCAGAGTTAAGA[A/G]CTAAACCACTTCTCA | 57630 |
| rs548314028 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223410 | ATGGCCCTAAAAGGA[G/T]GGGTAGGAATTAGAG | 57630 |
| rs548337052 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249561 | ACACTCCACTGGAGA[C/T]ATAAGGGTATTCTCT | 57630 |
| rs548343066 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123887 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 57630 |
| rs548357455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219016 | TCCTCCCTCCAAATA[C/T]AACTTCCCAAAAAGT | 57630 |
| rs548374999 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255239 | TACAAAATCAGTACG[C/T]GAATATTTTAACTAT | 57630 |
| rs548408648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116813 | ATCCCCAGACACTAT[C/G]TATTGTCCTTCCAGG | 57630 |
| rs548408900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102130 | TGACCTGGGTGAGTA[A/G]CCACTTACTGCTTTC | 57630 |
| rs548418659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201270 | AGAGCTGGCTTTAAC[A/G]ATTGACGAATACTTA | 57630 |
| rs548425161 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126516 | GGCTACATATTGGCT[A/G]TTCTGAGAATCTGAC | 57630 |
| rs548468541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101106 | CATCTGTGTCCGTCT[C/T]GTTTATTCTACCAAA | 57630 |
| rs548486632 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268677 | GATGGGGGAAAAAAA[C/T]ATTCAGAGGTATAAT | 57630 |
| rs548488459 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223293 | CACCACACCTCTCCA[C/T]AAAATGCAGCACATA | 57630 |
| rs548502714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144597 | ATGGATTAAGGATAG[A/G]AGGCACAAATTCACG | 57630 |
| rs548509261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259387 | GAAATGGCACCTCCA[C/T]TCCCTTCCCAGCTAC | 57630 |
| rs548522597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217248 | TTGGTTCAACACCCT[A/G]AGCTGGGTTGGCTTG | 57630 |
| rs548524884 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094634 | GAATATTATGACACA[C/T]TGGTGTCAACTTACA | 57630 |
| rs548561488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180287 | AAACTGAAAACCTGT[A/T]CAGAAAAATGCACCC | 57630 |
| rs548591071 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131426 | ATGTCACACTTCTTA[A/T]TAGACAGAGTCTCAC | 57630 |
| rs548596731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231421 | AAATACAAAAATTAG[C/T]CAGACGTCATGGCGC | 57630 |
| rs548626198 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191314 | AAAAAAAAAAAAAAA[A/C]ACCTTAGGAATATAC | 57630 |
| rs548646723 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235548 | CTGTGACAGAGCTGG[C/T]ATTTCAGCCCAAGCA | 57630 |
| rs548675998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124659 | TGAAGATCAAGAAAC[C/T]CTGATTAAAATCAGA | 57630 |
| rs548683407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120001 | ATCTAAAGCTCCTGT[C/T]ACTCTATAACAGGGT | 57630 |
| rs548695559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246709 | AATCAAATTACCAAG[C/G]AGCAAATTTAATTTT | 57630 |
| rs548695649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238243 | GGTCAGAATTAGGGT[C/G]TACCTACACCTACCT | 57630 |
| rs548725501 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178157 | GAGGCAGAAGAATCG[C/T]TTGAACCCAGGAGGT | 57630 |
| rs548771002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261020 | CAAACCTCTTGTGAG[C/T]GTGTACTCTGTGCCA | 57630 |
| rs548777010 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174049 | CTGAAGCAGCCCCAT[A/C]CTGATAACACAATAA | 57630 |
| rs548782377 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189209 | ACCACAATAAGCAAA[C/T]ACAATACCATTTCCC | 57630 |
| rs548800179 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241501 | AAAGGCCTTAGGAAG[G/T]AAAGGCCTTAGGGGT | 57630 |
| rs548807396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269638 | AAGTGGTATCAGCTG[C/T]CTTAATAAAGTCTTC | 57630 |
| rs548809948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225511 | ATCATGCTGTGTGCA[A/G]GAGGGTTAAAAGCAC | 57630 |
| rs548826914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128418 | TAACTGTTCAGGAAA[A/C]ATTAAAAACGAAAAT | 57630 |
| rs548868599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137989 | ATCATTCAGAAATAA[C/T]AGGCAGTAACGCCAG | 57630 |
| rs548875384 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217382 | GTCACTGGGCAACAG[A/C]GAACTGGTCCAACAA | 57630 |
| rs548889391 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130730 | AGGAACAATGTCAAG[A/C/T]CAAATTAGTTGTTTT | 57630 |
| rs548916488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264412 | CCCAAATATGGCCAC[A/G]TTGTGAGGTACTAGG | 57630 |
| rs548923740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243163 | TTGAAATGTTATTCT[C/G]ATTACAACTACACAA | 57630 |
| rs548950508 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166733 | CATCCTCTCTAGGTG[G/T]CACAGAGGCAAGAGA | 57630 |
| rs548971058 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142718 | TCCTTCCCCAGATAA[C/G]TCAGTCACTTTGAAG | 57630 |
| rs548996086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242344 | AATTTTTCCTATCAA[A/G]CAATGTTTTTAAAAT | 57630 |
| rs548996391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097905 | TGTGAGGACACTCAA[C/G]ATCTCTATGGAGAGG | 57630 |
| rs549016123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127415 | CACAGTCTTCGGAAC[C/T]AATTCAAATTTTAAA | 57630 |
| rs549016779 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202809 | AACTTTGTACCTAAA[C/G]TAAAGCTTAATAAAT | 57630 |
| rs549044857 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188810 | TCTATCAATTTGGTG[C/T]GTGTGCTTCAAGCTT | 57630 |
| rs549081701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106115 | ATATATTTATTATTA[C/T]TATTATTATTATTTT | 57630 |
| rs549089980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207441 | CAAATAAATAAGTAA[C/T]TTTAAAGAGAAATGA | 57630 |
| rs549112328 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150009 | TTCTCTCATTCCCTA[C/G]AAGAGGAAGCTAGCA | 57630 |
| rs549134905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099528 | TTGCCATGTGGGGCA[A/C]GTTAAACATTTAAGG | 57630 |
| rs549165211 | in-del | -/G | 0.00399679 | 0.0445244 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211498 | AAAAAAAAAAAAAAA[-/G]AAGAAGAAGAAACTA | 57630 |
| rs549205277 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147811 | CACACATGCTGGACC[A/C]GTATAGAATATTCAT | 57630 |
| rs549208774 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206967 | AAGACCCCATTTCTC[-/T]TTTTTTTTTTGAGAC | 57630 |
| rs549209505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169197 | TACTTCAGGAAAATA[C/T]CTTCTTACTTTGAAA | 57630 |
| rs549226159 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142650 | CACTGGTTTGAAATG[C/T]CATGTTTTAAATGTA | 57630 |
| rs549233478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176317 | ATCCTTTGGAATATC[C/T]AGCATTTTCATCAAT | 57630 |
| rs549270749 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272113 | TACAAAAAGTTATCC[C/T]AAATACCCCTCCTCA | 57630 |
| rs549282241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237239 | ATGTTCCCAGACACA[C/T]GGTGAAGGTGATTTG | 57630 |
| rs549289614 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169560 | TGAGACTGCACCACT[A/G]CACTCCAGCCTGGGC | 57630 |
| rs549327798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141795 | GGCAAGTGCCACCAT[A/G]GCCCGCCTAATTTTT | 57630 |
| rs549355856 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211211 | CACGGTGTTGAGCAC[A/G]GTGGCTCATGCCTGT | 57630 |
| rs549403093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206562 | CCATCAAGGGATTCA[C/T]TTTAAATAAGTGAAG | 57630 |
| rs549407272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228566 | TTCCACTTCTAAAAG[C/T]CCCAGTGATTACACT | 57630 |
| rs549432471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192427 | AATGCAAATGAAAAC[C/T]ATAATGCGATACCAC | 57630 |
| rs549443868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257322 | TGCTTAATGAATCCT[A/G]TTTTCTATATCCTGT | 57630 |
| rs549453133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157036 | AAGCTTAACTTCCTA[C/T]ATTAACTACTTTATT | 57630 |
| rs549483931 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261299 | ACTGTCATTGTAAAG[A/G]AGCTTTATTTGTCCT | 57630 |
| rs549491363 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104826 | GAATCACTTGAACCC[A/G]GGAAATGGAGGTTGC | 57630 |
| rs549512340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176349 | ATTTGAATGACGGTA[C/T]ATTAGGGCATATTTA | 57630 |
| rs549526441 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095984 | AAATTAGAGAACTGG[A/G]ATTTCTATCTTAAAG | 57630 |
| rs549543835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169639 | AAACTCAGACATCCA[A/T]GGAAAACTGGTTTTG | 57630 |
| rs549545699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162350 | CAAATATGATTTGGC[C/T]ATCACTACTAATGTT | 57630 |
| rs549549219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228546 | CCTTGTCTTCTGCCT[C/T]GCTATTCCACTTCTA | 57630 |
| rs549552389 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186632 | AGTCAAGAAAATAAA[C/T]TGAACTTAAAGGAGA | 57630 |
| rs549585187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236515 | ATATCGTTACTTATT[A/G]GTTGGTGTGACCTTA | 57630 |
| rs549628856 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121853 | GATAAAAAGTTCAAA[C/G]AGGAGTTGTACAAAA | 57630 |
| rs549656159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192950 | GATGGAATACTACTC[A/C]GCCATAAAAAGGAAT | 57630 |
| rs549662784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105612 | AAGAAGAGAGTTCTT[C/T]GCTAGACATCGTGGC | 57630 |
| rs549672114 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108587 | GCTTGACCTGGGCTA[C/T]AGATGAGCAGAGCCA | 57630 |
| rs549712884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257435 | CAAAATTATCAACAA[C/T]ATCCTTTTCACTCTC | 57630 |
| rs549719353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192583 | AACAGCGTGGAGATT[A/C]CTTAAAGAACTAAAA | 57630 |
| rs549772600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142298 | GTGCTCTTTAACTTA[C/T]ATGTATATATGTGTG | 57630 |
| rs549778208 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244039 | TTTGAACTGCATTCC[C/T]GTTCATTTCTGATTT | 57630 |
| rs549817572 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229580 | TTAAAAGTCCTCTAA[C/T]TTTGTTTAACATCAC | 57630 |
| rs549839142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236031 | CTAAGTGACAAAACT[A/G]TTCTGGACAACATTT | 57630 |
| rs549864881 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113351 | CTGACCTCAGGTGAT[A/C]CACCAGCTTTGGCCT | 57630 |
| rs549866708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244913 | CCAAAAATACAAGTC[C/T]AGTTTTTAGAAAAGG | 57630 |
| rs549890843 | snp | C/T | 7.68787e-05 | 0.00619947 | missense | SH3RF1 | GRCh38.p7 | 4:169130138 | GGGTCACAATTAACC[C/T]GGTGGTACTTATATG | 57630 |
| rs549899488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201034 | CAGGATTCCAAATAT[A/G]AAGAAATTAAGATGG | 57630 |
| rs549909546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143753 | AACTACCTGGCTGCA[C/T]TAGGTTAGGAAGGTG | 57630 |
| rs549928017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252058 | TGGTATGTTCCGCAG[C/T]GACTCAAGAACCACG | 57630 |
| rs549937427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231329 | TCCCAGCACTTTGGG[A/G]GGCCAAGGCAGGCAG | 57630 |
| rs549941798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105647 | GCCTGTAATCGCAGC[A/G]TTTTGGGAGGCTGGG | 57630 |
| rs549951055 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141804 | CACCATGGCCCGCCT[A/G]ATTTTTGCTTTTTTT | 57630 |
| rs549953300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163554 | CAAACTATAACCACA[C/G]TAACAAGGATAATTC | 57630 |
| rs549953748 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168674 | TTAAATATTGCAGTG[A/G]ATTATGATATCTTTC | 57630 |
| rs549996335 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231561 | ACACAGCGAGACTCC[A/G]TCTCAAAAAAAAAAT | 57630 |
| rs549998744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230745 | ACACCTGTAGTCCCA[C/G]CTACTCAGGAAGCTG | 57630 |
| rs550006094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265582 | AGGTTCAAGCGATTC[G/T]CCAGCCTTGGCCTCC | 57630 |
| rs550059770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237294 | TATTTTCAAAAGCAT[A/T]AATTTTCCAAAGGTG | 57630 |
| rs550060188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222431 | GATTGCACCACTACA[C/T]TCCAGCCTGGGTGAC | 57630 |
| rs550060211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264008 | CTGGACCACTGCCAG[C/T]TTCTGGGGAAACCAG | 57630 |
| rs550067656 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265038 | CACAATTCACCCTCA[C/T]GCTAAATGCAGGTCT | 57630 |
| rs550070195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099730 | ATAAAATGCACTAAA[C/T]CAATTTTGTCAAAAA | 57630 |
| rs550078011 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194735 | AGGAGTGAAACTGCT[A/C]GATCATAGGGTATGC | 57630 |
| rs550089001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177512 | AATGAGCACACAATA[A/G]ATTTGTAAATGCAAT | 57630 |
| rs550100081 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140017 | ATTTGATTTTTATGC[A/T]TGGACAGTAATATTT | 57630 |
| rs550118797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248435 | AAGTGGGAGTCGAAT[A/G]ATGAAAACACATGGA | 57630 |
| rs550128355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127626 | GGCACAGTAGACATA[C/T]TGTTTAATCAACCTT | 57630 |
| rs550130090 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273084 | TTTTTGAGACGGAGT[A/T]TCACTCTTATTGCCC | 57630 |
| rs550135322 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103076 | CAGGTGCCCGCCACC[A/G]CGCCTGGCTATTTTT | 57630 |
| rs550136065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193035 | GAAGTAACTCAGGAA[C/T]GAAAAACCAAACATT | 57630 |
| rs550182182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248000 | ACCACAGATGCTGGC[A/G]AGGATGTGGAGAAAC | 57630 |
| rs550226101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251411 | GTCAAGCAGCCTTAA[A/C]ATCGTGCACAAAACA | 57630 |
| rs550226397 | in-del | -/AAAC | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228950 | ATTCTGTTCTTCGAA[-/AAAC]AAACAAACAAACAAA | 57630 |
| rs550247048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144661 | ATGAAGAAGGCCAGA[C/T]AGAGACCAACAGAGA | 57630 |
| rs550323118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223917 | ATATTTAAGAACAGC[C/T]AGAAGGCCAGTGTAG | 57630 |
| rs550337792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108872 | TAGAGGCTGAGAAAA[C/T]ACTGGAAGAGGATGA | 57630 |
| rs550353093 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241012 | GAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCA | 57630 |
| rs550385864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254502 | CATTTTTCAATTCCT[A/G]TTGATAGTGGCCAAT | 57630 |
| rs550417431 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155196 | CCAGCAAATGGAATA[A/C]ACAGGAAATAGTGTA | 57630 |
| rs550447121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261557 | AATGTATAGTGAGCC[A/G]TAAACACTCCAACTG | 57630 |
| rs550461026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240888 | ATTATCACCCAAGCA[A/T]CCCCCTCATTGCAAG | 57630 |
| rs550475790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226588 | AACCATTCCTTACCC[C/G]CCTAGAAAGGGAGAT | 57630 |
| rs550478252 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127987 | ATCCGAAATGCTCCA[A/G]TGAGCACTTCCTTTG | 57630 |
| rs550527085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186746 | GCGTGGTGGCTCATG[C/T]CTGTAATCCCAGCAC | 57630 |
| rs550533610 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150780 | ATCCTGAAACCAACG[A/C]CCTGTGGATACTGAG | 57630 |
| rs550538982 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233618 | AACAAATGTGGTTGT[C/T]TTAGATGGCTTTGGT | 57630 |
| rs550544082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203736 | CACAAAAATAACTGT[A/G]AAACGAATGACTGAA | 57630 |
| rs550569185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263156 | AACAACTCCTTTGTC[C/T]GTCAGTGTTTGTAGT | 57630 |
| rs550578151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152812 | CTTACTCCAGTGCAC[A/G]TGGAGATCACAGTCC | 57630 |
| rs550630471 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271055 | CTTTCCCAGCCAAGG[A/T]GGGCGGAGGAAGAGG | 57630 |
| rs550639107 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146026 | TTCTATATAAAATAT[A/T]ACATATTCTATATAT | 57630 |
| rs550642532 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246146 | ATTCATGCAAATTGT[A/G]TATTACTATGCAAGG | 57630 |
| rs550662284 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238306 | GGAACTACCTACCAG[C/G]TGTCATGGGCATGGA | 57630 |
| rs550692802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270501 | AAATAAATGCGCAGG[C/G]TTAAGTTGCGAAACT | 57630 |
| rs550712377 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186257 | TTGTTAACAAATTTT[G/T]GGGGCAATGAAATAA | 57630 |
| rs550742259 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259545 | AGGATTGCAGAGCCA[C/T]GAAAAAGGGTGCCTG | 57630 |
| rs550744096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166422 | AAAATCCTATCCTTA[G/T]TAGAGGAATTGGCAG | 57630 |
| rs550745901 | in-del | -/C | 0.0676543 | 0.171026 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271452 | CCGCCTCCTCCTCCC[-/C]CCCGGCGGGGCTGGG | 57630 |
| rs550746113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159508 | AAACTCCAGAGCCAG[A/G]TTGCAGGGTGTGAAT | 57630 |
| rs550755393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133428 | TGCAGTGAGCCAAGA[C/T]TGTGCCACTGCACTC | 57630 |
| rs550773002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167699 | AAATCACAGTAGTTG[C/T]CCATAGGAGGTGGGC | 57630 |
| rs550798970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182862 | TCTTCCAACCAAAAA[A/C]AAAAGGAGAAAGGTG | 57630 |
| rs550878543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219472 | TTTCAGGTTTTTCCT[C/T]CTAAAAGAAACTATT | 57630 |
| rs550880718 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197181 | TAATTTTTGTATTTT[A/T]AGTAAAGATGGGGTT | 57630 |
| rs550887433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125798 | AACAGTCCTTGTGTG[C/T]ACTGAACTCAGATGC | 57630 |
| rs550893064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153566 | CTGTAAGACAATCGA[C/T]ATTACTGAAATAGTT | 57630 |
| rs550906703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264245 | CAACTCTCCTTGGTT[A/G]GTAAGTGGCATCTTC | 57630 |
| rs550912545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161737 | AATTTAATAACTCAG[C/T]TATATCTAAATTGGC | 57630 |
| rs550912857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233790 | TCATACTTGTCAGCT[C/T]TGCCCTTACAAGCTG | 57630 |
| rs550937209 | in-del | -/ATAAGAA | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237793 | ATACCCTACAGTCTT[-/ATAAGAA]ATAAGAAATAAGCTT | 57630 |
| rs550943285 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208004 | TGGGAACCAAAACAA[A/C]ATTGAATGAGCATAG | 57630 |
| rs550948735 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197851 | ATTATATCCCTTTAA[A/C]ATACTACTAAAAGTG | 57630 |
| rs550972253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111238 | CCCAGGAGGTAGAGG[C/G]TGCAGTGAGTCGAGA | 57630 |
| rs550975700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249090 | AAAATTAGCCAGGCA[C/T]GGTGGTGGGCGCCTG | 57630 |
| rs550981724 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152278 | TCAAAGCAAGAGAAC[A/C]CTTACCCTTATCTTA | 57630 |
| rs551000473 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234842 | CCTGATAGTTGTTTG[C/T]TGGGGAGCGTGGCTG | 57630 |
| rs551030188 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175585 | CAGAAGGCTTCCCTG[A/G]TTATCCCACAATAGC | 57630 |
| rs551041885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104072 | TGTTAGAAAGGAGCC[C/G]CTCTAAGAGGAAGGG | 57630 |
| rs551049921 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175649 | ACCCTGAACTTTCTA[C/T]CCTGCTCGTTTTCTT | 57630 |
| rs551064716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227485 | TCTTAACAGGTATCA[A/G]GCATAGAGTTGGAAT | 57630 |
| rs551075934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203862 | AGAAAATAACGCAGA[C/T]ACTGGTACTAAACAG | 57630 |
| rs551079845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190702 | ACAGAGAAAGAGGGA[A/G]CCCTCCCTAAATCAT | 57630 |
| rs551080341 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126761 | GCTAATTAAAAAAAA[A/T]TTTTTTTTTTGTAGA | 57630 |
| rs551091714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148466 | ATTAAAGCATAAGGA[A/G]AAAGAATGGAAGGAT | 57630 |
| rs551111398 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206764 | AGAAAATGACATGTA[C/G]CGTTGCATTCATTTT | 57630 |
| rs551115579 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172366 | GCCCGTACATGGATA[C/T]ACCTGTACTCAGAAA | 57630 |
| rs551128796 | snp | C/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272563 | AATGGAATGGAGAAT[C/T]TCTAGTCCAGTTTGC | 57630 |
| rs551129486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102563 | GTCATATACTTTCTT[G/T]TATTTGCCATCCCTT | 57630 |
| rs551135699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183477 | GTAGAGACAGGGTTT[C/T]ACCATGTTGGCCAGG | 57630 |
| rs551156273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242402 | GTGGAAAAAGAGATT[A/T]GAAATATTAAATTCA | 57630 |
| rs551171023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248543 | CCTAATGCACGCCAG[A/G]CTTAAAATCTAGATG | 57630 |
| rs551206911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126702 | GATCCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG | 57630 |
| rs551209169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205381 | CATAAAAACTAATTT[A/G]TATTTTTGTAATCCC | 57630 |
| rs551250357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234405 | ATCTCAGACGAAATA[C/T]CATGGTCTTCCAGTT | 57630 |
| rs551270427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118894 | ACAGCCAACTCTAAA[C/T]ATCTATTTACTCACT | 57630 |
| rs551275095 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210827 | GTTCCATTTTCTGTA[C/T]ATCACTTTCCTCTCT | 57630 |
| rs551275763 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271220 | TGCGCCCAGTACCCC[A/G]CCGGAGCCCGGGGGC | 57630 |
| rs551275798 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181988 | ATGAAGAGAGAAACC[A/G]TATTTGTTTTATTTA | 57630 |
| rs551288523 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117349 | AGGCTTGAAGTAATA[C/T]GCAGGGCACGCTTAG | 57630 |
| rs551309075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241476 | ATTTTAATCCATCAT[A/C]CATGGAAGTAAAGGC | 57630 |
| rs551312143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213498 | ATATTCTCTTGACAG[C/T]GTCTTTTGCAGAGCA | 57630 |
| rs551347842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197790 | TACTACTACAACTAA[C/T]AAATGATGAAATTTC | 57630 |
| rs551356062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141130 | ATGAAGTAAAAAGTA[A/G]AAGGCCTCAGCCAGT | 57630 |
| rs551432400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149176 | ATGGAAAGCAAAAAG[A/C]AACTCTTAAATTAGA | 57630 |
| rs551458238 | in-del | -/CT | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268472 | TACATGTAATTATGA[-/CT]CTGAGCCCCATCAAA | 57630 |
| rs551485761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263307 | TTATTCTATATCTTA[A/T]CCCACCCCCTGATGC | 57630 |
| rs551512321 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187934 | TGGACCCTAAATCCA[A/G]TGCCTGATGAAGGCC | 57630 |
| rs551534088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110159 | GCGGCAGGATTGCTT[C/G]AGCCCAGGAGTTGAG | 57630 |
| rs551543866 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119172 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAGCCT | 57630 |
| rs551544003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152874 | AGTTGAGGACAGGAA[A/G]AGAGGGCAAACTATT | 57630 |
| rs551544513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255014 | GGATGAAAGGAATGA[C/G]AGTACATTGCAAGGA | 57630 |
| rs551553447 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141882 | CAGTGGCGTGATGTC[A/G]GCTCACTGCAAGTTC | 57630 |
| rs551559657 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117101 | TTGGGAAGGTTTTCA[G/T]TGCTACAGAACTAAG | 57630 |
| rs551564960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161823 | GCACAAAGAAATCAT[A/G]GTAATAGAAAGTACC | 57630 |
| rs551595617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212929 | TGCTTTTTCCAGAAT[A/G]TAATATAGTTCAAAG | 57630 |
| rs551598890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173938 | CCCACACACCACCAC[C/T]ACCAAATACCTGACT | 57630 |
| rs551605216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119936 | AAGGCTTCTTTCCTC[A/C]GTGACCAAAAGCTGA | 57630 |
| rs551668801 | snp | G/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183924 | ATGAGACTACAAAGA[G/T]AAAGCTGACAGACTG | 57630 |
| rs551680378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191236 | ATCAGTAGCTCTTCT[A/G]TATACCAACAGCGAC | 57630 |
| rs551734123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111340 | GCTCACTGTAGCCTT[G/T]ACCTCCTGGGCTCAA | 57630 |
| rs551739941 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171606 | CATGATTTAGAAGAA[C/T]TTGGCCAGCTAAACT | 57630 |
| rs551766213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159296 | ACTATATTATGTATT[C/T]CTTCAAGGCTAGTTA | 57630 |
| rs551767090 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242438 | CCTAATAGCTAAGAT[C/T]TGCACTTACATTTTG | 57630 |
| rs551768772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162208 | ACAACAAAAAACATG[C/T]TGGCTTTTCCCTACA | 57630 |
| rs551786136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205616 | TTAAAGTGTTGACAA[A/C]TACGCACCTGTCAGA | 57630 |
| rs551801363 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213682 | GGTCCATTTTGAATT[A/T]ATTTTTGTGAAGAGT | 57630 |
| rs551821259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267657 | GTGATTAAAATGGTC[C/T]ATATACTTAAATACT | 57630 |
| rs551853642 | in-del | -/CCT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101816 | CCGGTCCCTGAATGG[-/CCT]CTGCCTCTTGGTGGC | 57630 |
| rs551877495 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271865 | TCAGGTGGGCTGGCA[A/C]CGCAAAGCACGCTGA | 57630 |
| rs551877538 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128919 | GAGCCCAAAAAGGAG[A/G]TCAATAATGTTCATC | 57630 |
| rs551883489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142553 | CATAAAGAATAAGGT[C/T]GGGAAAGCATTTAGC | 57630 |
| rs551898822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098779 | GTTAGAGCAGCTTAA[C/G]TTTGGGCCAGTTATC | 57630 |
| rs551899576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165083 | TTTACTGGGAAGATT[A/C]TCTGCAGTAACTTGA | 57630 |
| rs551945321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130559 | TGGCTGAACACTCAC[C/T]TGTCTATCAATACGT | 57630 |
| rs551947984 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176195 | CCAGTCAGGTATTTT[A/G]TCCTAGCAGCCCAAG | 57630 |
| rs551948738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192546 | GCTGATGGGAATGTA[A/G]ACTAGTACAACCACT | 57630 |
| rs551960138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236095 | TTCTAGCCACTGGCA[C/T]AGCATCTGTAGCCCA | 57630 |
| rs551964568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172137 | TTGATACTGTATGAG[C/T]CTAAGAAAGCAAGAG | 57630 |
| rs551969549 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243030 | GCATTGCATGAAAAA[C/G]AACTCATTTCCAAGA | 57630 |
| rs551997431 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224465 | TGGGATTACAGGCTC[A/G]CGCCACCATGCCTGG | 57630 |
| rs552057456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112504 | ATGACCTGAAACCCA[A/G]AAGGGAAGATGCTTC | 57630 |
| rs552075197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195374 | TTTGTTTCTGCTTTT[A/G]TTAGCATTACAGTGA | 57630 |
| rs552127605 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206514 | TCCGTCTCCATAAAA[A/C]ATTTTTAAAAATTAT | 57630 |
| rs552182972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107794 | CACTTCTCACATGTC[A/G]CCACCTTGATTAAAT | 57630 |
| rs552206187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115955 | AGGAAATTCCTCCAC[A/G]AGACTGTAAGCTGCA | 57630 |
| rs552221042 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181006 | GCTCTAGGGACCAGA[C/G]GATGCTGTATTCTTT | 57630 |
| rs552248192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101394 | GCATGATTCCACTTA[G/T]GAGATGCCCAGAAGT | 57630 |
| rs552255941 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094785 | TACATTGTTTTTTTT[A/T]AAAAAAAAGGTTAAT | 57630 |
| rs552302825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216346 | GAAGTTTAAGCATTT[A/T]AAAATTTTCATTATT | 57630 |
| rs552328964 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212157 | GCAACCCCCGCCTCC[C/G/T]GGGTTCAAGCGATTC | 57630 |
| rs552339144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203256 | AAAGAGCAAATAAAA[A/T]TATCCCAGAACTGGC | 57630 |
| rs552373746 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160369 | TTCCACAAAACAAAT[A/C]TATTACATGTTCCTA | 57630 |
| rs552397981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109593 | ATTCTGATTTTTTCT[A/G]TGTTAGCAGAAGAAT | 57630 |
| rs552399878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194452 | TGCCTTTTAAAATGT[C/T]ATTTAAATGGATCAT | 57630 |
| rs552416731 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154664 | TTATCCATCACACAG[A/G]TATCTACTAAGACCT | 57630 |
| rs552420573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188625 | TGTAATTCACTGAAA[A/G]TCTGACAGGAAAAAA | 57630 |
| rs552423707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246376 | CCTCGGTGTGCTATA[C/T]AGATATTATCACTGA | 57630 |
| rs552451008 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202497 | GGAGGGGATGTGGTT[C/T]CTTTTAAAGGACAAT | 57630 |
| rs552514659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210003 | GGTTCGCCATGTTGC[C/T]CAGGCTGGTCTCAAA | 57630 |
| rs552514694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201984 | GAGAGGAGTCTTTGG[A/G]CACAGTATCTAATGT | 57630 |
| rs552535503 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244509 | AGAACACACTACACC[A/G]TCAATGGCAGAATGT | 57630 |
| rs552539053 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121581 | GTGCCCACGAACACA[C/T]GGTAACCAGGCAGGC | 57630 |
| rs552557167 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125618 | TCTCTTACGTGTGTA[C/T]CTCCCTCACACACTC | 57630 |
| rs552565277 | snp | A/C | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096179 | AACGTATCTATTATA[A/C]GAAAAGTTCAAGTTT | 57630 |
| rs552567672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225118 | AGGTATTACCAAGAC[A/T]AGGTTAGTGCCAGTT | 57630 |
| rs552574150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166525 | TGAAAAGAAAAAGGA[C/G]AAAGTTCTTGCAACT | 57630 |
| rs552574430 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214238 | TGGCACCTCCTCCCT[C/T]ACTCTCTTGCTTCTG | 57630 |
| rs552575814 | in-del | -/ATAG | 0.00119737 | 0.0244387 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272982 | GCAGCACACAAGGTC[-/ATAG]ATAGAATGGTGCAGC | 57630 |
| rs552601487 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153798 | GAAAATGCTCATTTG[A/T]AAGAAAAGAAGCAGA | 57630 |
| rs552616570 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110199 | GGCAACATAGCAAGA[-/C]CCCATCTCTACCAAA | 57630 |
| rs552622881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269731 | ATCCAACTAAATTCC[A/C]TTTTTTAAGCCACTT | 57630 |
| rs552636644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252863 | ACCCACAGTAACAGG[C/T]AGGATGGGTGGATTA | 57630 |
| rs552668406 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123436 | ATAAAGATTTTTCCC[A/G]CACTGTAGCTAAAGT | 57630 |
| rs552696783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138135 | GCATTTTCAAGGCAA[C/T]TGGCCAGGAGATCCA | 57630 |
| rs552698056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252398 | ATATACAATATTCCA[C/T]AGGATCAGCTTTTAA | 57630 |
| rs552715042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246410 | ATCAAACTGAGCTAG[A/G]AGTATGTGCAACCCC | 57630 |
| rs552717437 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140745 | TTTAAAGAGAAAAAA[A/T]TTTTTAATAAGAACT | 57630 |
| rs552731459 | snp | C/T | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093903 | CCATGCTGAGACTTA[C/T]GGGTTATCATACTAT | 57630 |
| rs552732040 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120461 | GCCTGGCATATAGTA[C/T]GCATTATATAAACAC | 57630 |
| rs552733129 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197131 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 57630 |
| rs552750194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152894 | GGCAAACTATTCCGG[C/T]AGCATTTCTCACCAC | 57630 |
| rs552753127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167279 | TGATATATTATAATG[C/T]GTTCATTAGAATGAT | 57630 |
| rs552757947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131139 | CCCAGAGGACCTAAT[A/G]GAAACTTTCAGTTTC | 57630 |
| rs552758519 | in-del | -/ATTA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205445 | CAAGTGCTATCTCTT[-/ATTA]TTATATTAATAACTG | 57630 |
| rs552786086 | snp | A/C | 0.145978 | 0.227331 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219991 | GCGTGTGGTACTCTA[A/C]ATTACAGGAAAGACA | 57630 |
| rs552802287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270241 | GGCTGCACCCCCGCT[C/T]CCACGGCGCCAAGCA | 57630 |
| rs552807116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180912 | GAGCACCTATTAGCA[C/T]TCTCAGCACTAGCCG | 57630 |
| rs552826432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144367 | CCCAAACAAAAATAT[C/T]CCATTCAAAATATTC | 57630 |
| rs552868649 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261577 | CACTCCAACTGCACT[C/G]CAACCTGGGCAGAAG | 57630 |
| rs552873944 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124325 | AAAAGGACAAAAATC[A/G]TCTATGCACCTGATA | 57630 |
| rs552914610 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227377 | GTTCCTCTTGAATAA[A/G]CTGTATTTATCACCA | 57630 |
| rs552925800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132135 | ATTCTTTGTTCAAAA[C/T]GCGAAGTACATGGAC | 57630 |
| rs552968991 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094808 | AGGTTAATTTAGGAA[C/T]GATTTCATCTTCAAC | 57630 |
| rs552985411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194480 | CATGCAGGCTGTATT[C/T]TTTTGTGTCTGGCTT | 57630 |
| rs552988367 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095657 | GCCATTCTCAGACAG[G/T]GACTACAACTTCAAT | 57630 |
| rs552998261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138920 | TCTTCATATCATATA[C/T]TCTCCATTAAAATAA | 57630 |
| rs553016368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245456 | ATTTATCTATATAGT[C/T]CACTAAAATCTACTA | 57630 |
| rs553017298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188054 | ACTGCTGGCAACCAC[C/T]GAAAACTAGGAAGAA | 57630 |
| rs553021024 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166133 | ACAACAAAAGACACA[A/T]GAAGAAAATAAAAAT | 57630 |
| rs553025106 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261292 | CTGGTCCACTGTCAT[C/T]GTAAAGGAGCTTTAT | 57630 |
| rs553043711 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150478 | ACCTCAGATAGGTAT[C/G]ATTTTTTGTGGTGAG | 57630 |
| rs553046208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152611 | ACGTGGTGGTGCATG[C/T]CTGTAATCCCAGCTA | 57630 |
| rs553048607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194078 | ACTACCAAGAGAACA[C/T]CCCAACATTTTTTTT | 57630 |
| rs553066751 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102200 | TCACTGGCATAACCA[A/T]ACTAGTTCCCTTTGT | 57630 |
| rs553067362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131604 | CCTAAGGCTGTTTCA[C/T]GCTGACTTCCCAGAA | 57630 |
| rs553084209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173500 | ATGAAAAACAAGATA[C/T]AAATTGTCACTACAA | 57630 |
| rs553100361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217764 | AACTCTATAGATGGA[C/T]TCTGGCTAGTGATGG | 57630 |
| rs553125534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210700 | TAAAAAGACTGTAAA[C/T]TACCCTTGTGTCAAT | 57630 |
| rs553133406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197406 | AGGGCAGGTGGATCA[C/T]CTGAGGTCAGGAGTT | 57630 |
| rs553159155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225216 | AGCATCATGAAAGGA[C/G]AAGAGGATTTGAAAA | 57630 |
| rs553164827 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261200 | CAGCCCATGGCAGTG[C/T]TGGAACCAGAGGCCA | 57630 |
| rs553180113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107928 | TGATTTCTCTTTTTG[C/G]AAGCAAATATACAAA | 57630 |
| rs553185221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218551 | CCTGGTGCAAAAACT[C/G]CTTTTACCCTTTCCC | 57630 |
| rs553208623 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179488 | ATACAACCATATGAA[C/G]CAATATCCAAAATTC | 57630 |
| rs553221164 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261983 | TATGAGAAAAATACT[A/G]TGAAGAAAAATTCTA | 57630 |
| rs553234852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224743 | GAGATTATGACAGCT[A/T]GGCTTGGGTAGGTGC | 57630 |
| rs553260361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196036 | CCAGGCTGGTCTAGA[A/T]CTCCTGACCTCAGGT | 57630 |
| rs553298212 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231589 | AATTTTTTTTTTTAA[A/T]AAATAAATAAAAAGG | 57630 |
| rs553302473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211572 | AATAAGCAGGTTATC[A/G]CAATAGCACTTGTCT | 57630 |
| rs553306396 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093946 | CTGCTTTTCCTTCTA[C/T]GGCTAAGACAACTAG | 57630 |
| rs553309989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240564 | AGATACCAACGTGTA[C/T]TAAGGAGTTTTTGAG | 57630 |
| rs553323308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206033 | TTTAAATGGAATACA[C/T]AGTGATAAAACTGGG | 57630 |
| rs553369128 | in-del | -/CTAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269695 | CATTGAAAGTTTCCT[-/CTAC]CTGAAATTTACTTTT | 57630 |
| rs553370213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102687 | TTTCTGCTGTCATCA[A/T]TTATACATTTTCTGC | 57630 |
| rs553414541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109171 | GCTATTCTTGCCATG[A/T]TGTAAGAAAGCACAC | 57630 |
| rs553420352 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145728 | GCTGGGATTACAGGT[A/G]TGAGCCACCGCCTGG | 57630 |
| rs553421617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169345 | CTCACACCTGTAATC[A/C]CAGCACTTTGGGAGG | 57630 |
| rs553427319 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110107 | AGGCCGGGCACAGTG[G/T]CTTACACCTGTAATC | 57630 |
| rs553434472 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265870 | CATTGGAACTGCGCA[-/T]AAAAAGCAGAAACTA | 57630 |
| rs553454432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099218 | CTACCTCAGCCTTCC[A/G]GCTGGGACTACAGGT | 57630 |
| rs553485341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146291 | CTGCAGTGCAGTGGC[A/G]CTATCTCAGCTTGCT | 57630 |
| rs553490588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241005 | GGAGGCTGAGGTGGG[C/T]GGATCACGAGGTCAG | 57630 |
| rs553567550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118121 | AGAACAAGCTAGGAT[A/C]ATTCCCTGACAATAT | 57630 |
| rs553570445 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209160 | CAGACACGGTGGCAC[A/G]CACCTGTGATCCCAG | 57630 |
| rs553584524 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191300 | TTACAATAGCTGCAA[-/AG]AAAAAAAAAAAAAAA | 57630 |
| rs553599386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199701 | ACAGCTTCCAATCCA[A/C]TGGGAATAAGAAAAC | 57630 |
| rs553664335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116993 | CCTATTATTCATTCC[C/T]TTTTCTTATGAATCA | 57630 |
| rs553706088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223522 | CACTCATTCAGACAA[C/T]GAATGTTTACTGAAC | 57630 |
| rs553747204 | snp | A/G | 1.65225e-05 | 0.00287419 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122085 | TAAGCAGTAACAGAC[A/G]ACACGCTCACTTACA | 57630 |
| rs553752429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254583 | TAAAAACTAACCACT[C/G]GAGAGATGGGGGAAA | 57630 |
| rs553764072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214100 | GAAATGTAATCCTCA[A/G]TGTTGGAGGTGGGGC | 57630 |
| rs553767682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230132 | ACTGCTTGAACCCAG[A/G]GGCGGAGGCTGCAGT | 57630 |
| rs553769284 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228953 | TCTGTTCTTCGAAAA[-/AC]AAACAAACAAACAAA | 57630 |
| rs553770686 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222369 | ACTTGGGAGGCTGAC[A/G]CAGGAGAACTGCTTG | 57630 |
| rs553804808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264686 | TCGTCTCAGTCCCAA[A/T]GGTCCCTCTTTCTTA | 57630 |
| rs553821514 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148683 | AGTAAGAATGGTACA[A/C]ACGGGGTACTGTAGA | 57630 |
| rs553824533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163110 | AGGGAGAGAAAAAAA[A/C]AAACAAACTAGAGAT | 57630 |
| rs553829874 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249472 | AGTCTCTAGAACTGT[A/G]AGAAATAAATTTGGG | 57630 |
| rs553849276 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215519 | AGACTGTAGAGAGTT[A/G]GTATAATTTCTTCCT | 57630 |
| rs553853536 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246040 | TTTAAGTCAGAGCAA[C/T]TGAAGATGTGATGGG | 57630 |
| rs553871647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115441 | TCATAGGAGCATGAA[A/C]CCTATTGTGAACTGC | 57630 |
| rs553885281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149588 | AATGTCTTTAAATTT[C/T]ACTTACAAAAATTTA | 57630 |
| rs553933550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186792 | CAGGCGGATCACGAG[A/G]TCAGGAGATCGAGAC | 57630 |
| rs553936540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243391 | TACAGCGCATGCCTG[C/T]AATCCCAGCTACTCA | 57630 |
| rs553945933 | in-del | -/CGGC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141397 | CCATTTACTATGTCT[-/CGGC]TGGCAGGCTCGTACA | 57630 |
| rs553953951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236683 | GTAAGAACCCACTAC[C/T]GTCCCCAGAAATTCT | 57630 |
| rs553954777 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142919 | GTAATAAGGTTTTTG[C/T]TTTTGGATGACCTAA | 57630 |
| rs553983133 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100362 | TCTTTTTTTTTTAAG[A/G]CTGAGTTTCGCTCTT | 57630 |
| rs554005943 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119560 | TATCCATTATTATCA[C/T]TATTTTGCACCAGGG | 57630 |
| rs554007841 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127798 | CCATTTACTACATTG[C/T]ATAATTTTCAGCCCA | 57630 |
| rs554018563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258950 | ACTTTATACAAATGC[C/T]AGGGATATTTGTATC | 57630 |
| rs554036877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223966 | ATCAAAGAGGTAAGA[A/G]ATGTTGCTGGAAAGA | 57630 |
| rs554044113 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208485 | GACAGACACAAATGT[G/T]TCTTAAAAATATGAG | 57630 |
| rs554046707 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227132 | GATCATGCCACTGTA[C/T]TCCAGCCCGGGTGAC | 57630 |
| rs554070530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120425 | AAGGTTAATCAGTGT[A/G]ATGCATTTATAAATC | 57630 |
| rs554074474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250864 | GGAAGAGACATTTGA[A/T]AAGAGACCAAACTGA | 57630 |
| rs554079373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164481 | TGCTAATCCATCTTT[C/T]TGAAACTGTCCTCCC | 57630 |
| rs554103930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216560 | AGAAATGCTTTCTCC[A/G]CCAGGAATGGTTGCT | 57630 |
| rs554120135 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197290 | TATAGACATGAGGCA[A/C]CACGCCCAGCCAATT | 57630 |
| rs554140771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136252 | TCAGCCAGTGAGCAA[A/G]CATGTTTGTAAGTTG | 57630 |
| rs554144692 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267020 | AGAAGAAACATGAAG[A/T]AAATTAGGAAAAGCA | 57630 |
| rs554203317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178996 | GACCCTACCCATGTG[C/T]GCTAGGCATAATAAT | 57630 |
| rs554203958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129560 | CCAAGACTGAAGGTG[C/T]CTTTAAACAGCCACA | 57630 |
| rs554220323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157196 | AATCTCTTCCTGATA[C/T]TGCTTTTAATGTGGG | 57630 |
| rs554248783 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207669 | GGTTCTGGATGCTTC[A/G]AGCTTTGCTATGAAG | 57630 |
| rs554282100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169972 | ATTTCTCCATTATTC[A/G]ACTGTGCAAGAAATG | 57630 |
| rs554282818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236329 | CTGGAAGCATGTGCT[C/G]AGATGGAGCCTTTGT | 57630 |
| rs554283731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150528 | TCAGCATTTTTCAAG[A/G]ATACAATAATATACT | 57630 |
| rs554316630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099963 | ATCTTCCAGCTCAGG[C/T]CCTGATCTTGAGCCT | 57630 |
| rs554333205 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186945 | TGCGAAGCCAGGAGG[A/C/T]GGGGCTTGCAGTGAG | 57630 |
| rs554339097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265857 | TGATTCCTTAAATCA[C/T]TGGAACTGCGCATAA | 57630 |
| rs554354098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135165 | CAAGGTGAGACCCCA[C/T]CTCTATTAAAAACAA | 57630 |
| rs554387011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133247 | AAAAATGAATACTAA[A/C]ATTTTTAAGCCCCTT | 57630 |
| rs554395228 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162392 | GACGGCCAAGACGAA[C/T]ATTAAAGGTTTTATT | 57630 |
| rs554395619 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133141 | TATATGGTGTAGACA[G/T]GAGCTGGAAGGTGCC | 57630 |
| rs554414193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143405 | CCCACTCAGTTTGGA[C/T]GAGTCTCGCTGCAAG | 57630 |
| rs554499434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149738 | TAAAGGAAAATAATA[A/C]ATCTAAAGGAAAAAA | 57630 |
| rs554510421 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224214 | CTGTATGGCCTTGTG[A/G]TCATAAATATGATTT | 57630 |
| rs554530063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199734 | ACAAAATTCAAACAA[C/T]TTAAAAAGAAAGACA | 57630 |
| rs554538939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170955 | ACTGTAAAATAAATA[C/T]AGTAATTGAAGGAAA | 57630 |
| rs554581627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106440 | ACCTGCTCTAGTTGC[C/T]TCACAACTAGCAGGA | 57630 |
| rs554589496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206995 | GACAGGGTTTCACTC[A/G]TCACCCAGGCTGGAG | 57630 |
| rs554597005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107466 | TCTCCTCCTTCTCCC[G/T]TTCTGCTATATATTT | 57630 |
| rs554614204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250912 | TGTTGAGACCTGGGT[A/G]AAAGCTGACCTTCCT | 57630 |
| rs554621752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257659 | TTAGGTAATTCTAAA[C/T]ATGGTTCTAAAGTGC | 57630 |
| rs554640760 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215210 | CATCTACTGGTATGA[C/T]CATATAGTTTTTCTT | 57630 |
| rs554658516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108100 | TCTGAAACCTTAAGC[A/G]TGAATGTTCTTTCTG | 57630 |
| rs554681134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265301 | TATTAAATAAAGCAA[C/T]GAATAAACTAAGTAT | 57630 |
| rs554698099 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241684 | GCTATCTTTCTAAAA[C/T]GAAAAATAAAAAACA | 57630 |
| rs554708692 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216844 | TACACTTCCCATGGT[C/G]TTCCATTTTTAAAAA | 57630 |
| rs554709085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214722 | TTTTAGGTGCTAATG[C/T]AAATGGCAATGTGTT | 57630 |
| rs554730678 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179753 | TCATTCTTTGAACTA[C/G]ATTTGCTTCCAAGTG | 57630 |
| rs554743706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144064 | GGTGGACCACATAAA[C/T]TCCATGGTTTTGGTT | 57630 |
| rs554773448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236928 | AATATCTCCAAAAAC[C/T]ACAAAGTAGAAGAGA | 57630 |
| rs554827590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245230 | ACCAACTACTAACTG[A/T]GAAGTCAGAACTGGA | 57630 |
| rs554845228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202188 | GCAAATATTTATTAA[A/G]GGCCTACTTCGTGTT | 57630 |
| rs554857873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113508 | CATTTAGAAAGGGAA[A/C]TAAAACTCTTCCAGG | 57630 |
| rs554873811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253049 | AATGTGAAAAATAAA[C/T]TTGCCTCTCAAGGAA | 57630 |
| rs554890612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244228 | TACCCAGCAAATCAT[A/G]TTTGGCTGCCCTGCA | 57630 |
| rs554898568 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249101 | GGCATGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT | 57630 |
| rs554913087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227638 | TCTATGCATTATTTA[G/T]TTTACTATACTACCA | 57630 |
| rs554918116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105869 | GAAGCCTGCGCAACA[C/G]AGCAAGACCCTGTCT | 57630 |
| rs554995522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267192 | AAGACATTAAGTTGA[A/G]TGTTTGAGCCTCTCC | 57630 |
| rs555021598 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195906 | CAGGCTGGAGTGCAG[C/T]GGTGCAATCTCGGCT | 57630 |
| rs555034850 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175809 | TGCATTTTGCACTAT[C/T]TGTATCTTCCCTCTC | 57630 |
| rs555057751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126889 | GGCCATCACACCCAG[A/G]CTAAAATTTTAAAAT | 57630 |
| rs555074509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179114 | TATCCTGGCTTATCC[A/T]GGTGGGCTTACTGTA | 57630 |
| rs555113524 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266906 | TCCCCCAGCAAAGTA[A/G]CAGACATATTTCCTG | 57630 |
| rs555150201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129615 | CAAGAAATTAAATAA[G/T]GAATCTTTAATGTAG | 57630 |
| rs555172464 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228311 | TAAGATAACACAAAT[G/T]TGTTATCTTGCAGTT | 57630 |
| rs555182714 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112026 | ATTACAAAATTATAT[C/T]TCTCTGTGGAACAGC | 57630 |
| rs555187538 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159551 | CTCTGTGATTTGGGG[C/T]AGGTTAACTCGCTGT | 57630 |
| rs555235904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096844 | CTATTTTCTGTTTAG[C/T]AGAGACTTAGTACTA | 57630 |
| rs555246370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208664 | GAGTTTTGAATCAGG[C/T]ATCAAACATCTAGTC | 57630 |
| rs555251015 | in-del | -/A | 0.491368 | 0.0651254 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187012 | GCGAGGCTCCATCGC[-/A]AAAAAAAAAAAAATG | 57630 |
| rs555272702 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132679 | AGGCTAAGTAAGGTG[G/T]GGAAGAGTTGGGGTA | 57630 |
| rs555272974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259581 | CTGAATTTTTCTTTT[C/T]AAGGTTACTACCTTC | 57630 |
| rs555275705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165507 | GGTGATCTGGTGAAA[C/T]CCCATCTCTTAAAAA | 57630 |
| rs555279215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172213 | AGCCACGACCAGCTC[A/G]GTTGCTTGCTGAAGG | 57630 |
| rs555305013 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115359 | ATCTGTATTTACAGC[C/T]GCTCCCCATCACTTG | 57630 |
| rs555315836 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200423 | ATAAAAATAAAATCT[C/T]CACAGTTAGAAAATT | 57630 |
| rs555316774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204308 | ATTCAATGAATTTCC[A/G]GCACCTCATTTCATT | 57630 |
| rs555341718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255310 | TTTGAAGCATAGCAA[C/G]GCTCTTCACTGTTGC | 57630 |
| rs555342413 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175139 | TTGCACATCCACTTA[A/C]TGCATCAGCAAGTCT | 57630 |
| rs555347382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161366 | TTTTTGTTTCCAAAT[C/T]ATACATACAGGTTGT | 57630 |
| rs555348013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134470 | CTTAAAGCTATTCCC[A/C]TTCTGAGCTGTCACT | 57630 |
| rs555360479 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242496 | GCATAAAAATCTCCT[A/G]GGAAACTTGTTTGAA | 57630 |
| rs555374009 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130642 | ATGACTTCTACCTTT[C/T]GGTGGGGATGCATAA | 57630 |
| rs555388950 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164723 | TGGAAGTGGGCAGTT[A/G]AGTGTCTTATACTAA | 57630 |
| rs555401946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183123 | CCAGCCTCGCCAACA[C/T]GGCGAAACTCCATCT | 57630 |
| rs555409493 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134909 | AGTTGTGCGTTGTGC[A/G/T]TGTCTTTATTTCTCA | 57630 |
| rs555411040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175730 | TAAGCTCTAAAAAAA[A/C]TGTCTTGTTCAACAG | 57630 |
| rs555452399 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162889 | GTGGCTCCTCAGCAC[A/T]CACTCTGTGCTGTCT | 57630 |
| rs555463796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174759 | TCTAAAGCCCCACCC[C/G]AAACCAATTAAATAA | 57630 |
| rs555501024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234822 | TGGCACTACTGACAT[G/T]TGGGCCTGATAGTTG | 57630 |
| rs555506104 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256979 | GGAAAACTGAAGATA[C/G]TAATGTTTACTGAGC | 57630 |
| rs555517963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204852 | CTGAGCCCCGGCCAC[C/T]TTCTCCTTTTGAAGA | 57630 |
| rs555539350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169386 | CGGATCATATGAGGT[A/C]AGGAGTTCAAGACCA | 57630 |
| rs555546173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256115 | AAAGCACATCTAGTT[C/T]CCCTTACGGAAAGTC | 57630 |
| rs555580992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213056 | TTAGGCAAACACCAA[A/G]CAATGCACTAGATCA | 57630 |
| rs555598288 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272818 | AGGCCCTGTCTTTTG[C/T]ACAGGACCGTCATAT | 57630 |
| rs555607032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128754 | CTGGTCCTAAGCACT[C/G]TAGCAGAGGGAAATA | 57630 |
| rs555607520 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263411 | ATGCATTAATGTCAT[A/C]TTTGACCTAGTATAG | 57630 |
| rs555610291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161862 | TAAGAAGTAGAAAAA[C/T]GGGTGGAAGAAACAA | 57630 |
| rs555629668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256595 | GTCTGTTTTGTTTGT[C/T]TCTTTCCTTCTTTCT | 57630 |
| rs555676846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264756 | GACCCTTCACCCTAC[A/G]TGGCCCTTGGGGCAG | 57630 |
| rs555680571 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177975 | AAGAACTTTTTTTGG[C/T]TGGGCACGGTGGCTC | 57630 |
| rs555682862 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141965 | CTACAGGTGCCTGCC[A/G]CTACACCTGGCTAAT | 57630 |
| rs555691824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235630 | CTCATATAATAATAT[C/G]CCATATTAATCATTA | 57630 |
| rs555695911 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153271 | GGAGATACATCATCT[A/C]ATTCAATCTTCTCCA | 57630 |
| rs555710110 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170334 | GAGCCCATGCGTGCA[C/G]CTGAGACTACTTTTG | 57630 |
| rs555732589 | snp | A/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271288 | CCTAGAGGATGGGGA[A/G/T]CGGGGCCCCCAGGGG | 57630 |
| rs555733542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104946 | GAGCTTTGCACTTAA[C/T]GTAAGTAGGTTTGAA | 57630 |
| rs555734307 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167816 | GAAAGGTATCAAAAC[C/G]TACTAGATCGTACAC | 57630 |
| rs555771706 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106643 | AGGAAGGCTGGGGAC[C/G]AACCCATTAAGAAAC | 57630 |
| rs555778574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236215 | CTTGAAATGGAATCA[C/T]GGCCTAGTAACTCAC | 57630 |
| rs555783303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192183 | GAATCTACAATGAAC[C/T]CAAACAAATCAACAA | 57630 |
| rs555797248 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104490 | ACAGATGAGAGGAAA[A/G]ATAAAATGATTTCAT | 57630 |
| rs555808767 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202169 | CAATGGAAGTACTTA[C/T]TCAGCAAATATTTAT | 57630 |
| rs555842960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198790 | CTAACAAAGAAATAA[C/T]AATTAGGCTGAAAAC | 57630 |
| rs555850990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191490 | CAATCTACAAATTCA[A/G]TGCAATCCCCATCAA | 57630 |
| rs555858417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105075 | ATGGCTTCATCTGAA[A/G]TACAGAGGTAAGGTG | 57630 |
| rs555859797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221695 | TTTTATGTCTGATAA[C/T]AAAAAAAAGTTAACT | 57630 |
| rs555864940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184180 | CGACATCCCCTACTT[A/C]TGAAATCCATTTGGT | 57630 |
| rs555882524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154914 | ACTACACATACTCTC[C/T]AAAAAGACTTTACTA | 57630 |
| rs555941504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112841 | CAAGAAAGACACAGA[A/C]CCGCTGTGGAGGATG | 57630 |
| rs555967470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222883 | GTTCTAAAATGGCAA[A/G]TTCTCAGCTGTCTAT | 57630 |
| rs555984560 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253149 | ACATAGAATTCCCAC[G/T]TCTTACACACAAAGC | 57630 |
| rs556014960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175276 | CTAGCACCTATTATC[A/C]ACAGTCTTGCCTGTT | 57630 |
| rs556021597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228649 | AGCAACCTTAACTCT[C/T]TGCCATGTAATAACA | 57630 |
| rs556030570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221962 | CTCAAAGTAAGTCTT[C/T]GTTCCCCTCATCCAT | 57630 |
| rs556040545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213941 | GTAAGTCTTGAAGTT[C/G]GATGGTGTGAGTCCT | 57630 |
| rs556040578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205015 | GTAAACTAAGGAAAA[A/G]GAGGAATCATACATT | 57630 |
| rs556077333 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255808 | AGTCTCGTTCTGTTG[-/C]CCAGGCTAGAGTGCA | 57630 |
| rs556080527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126305 | GAGGTCTCAGTTCCC[A/G]AGATGCTAGAATCCT | 57630 |
| rs556118170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111613 | CATATATACATATAC[A/G]TAAGTATCTCCCAAA | 57630 |
| rs556126342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168770 | ATGACTGATGATCTC[C/T]AGTAATCTATGATTT | 57630 |
| rs556134082 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128817 | TAAAAACAAACCAGC[C/T]GCTTAGAAGCCTCCC | 57630 |
| rs556154398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236305 | GAACTCGACTTGCCA[A/C]TTCCCTTCCTGGAAG | 57630 |
| rs556160994 | in-del | -/T | 0.00601252 | 0.0544987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156309 | ACACAAAACTTGTAT[-/T]TTTTTTTTGCAAAAG | 57630 |
| rs556161062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221105 | ATTTTATACTGTTTT[C/T]GATTTGCTGACACAA | 57630 |
| rs556186311 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272518 | GCAAATACATGGGCA[A/T]TTGAGCTGAGAAAGA | 57630 |
| rs556215132 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256186 | TAAATTGAATTTTTT[A/T]AAAATTACTTGAGCT | 57630 |
| rs556216045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243288 | GAGGTCGAAGCAGGC[A/G]GACCACCTGAGGTCA | 57630 |
| rs556222428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227804 | AATGTCAAAGGGCTA[C/T]GGGATAGACAGTGGA | 57630 |
| rs556247147 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271454 | CGCCTCCTCCTCCCC[A/C]CGGCGGGGCTGGGAG | 57630 |
| rs556248406 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187451 | ACTCAGTCTCCCAAA[A/G]TGCTGGGATTACAGG | 57630 |
| rs556266432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162587 | ACTACATAAAATTTT[C/G]TAATCATACTAACTT | 57630 |
| rs556277238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242687 | TCATGGGGGCTCTGC[C/T]CTCATAAATGGACTG | 57630 |
| rs556279567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156026 | GCAGATATATTCCTG[A/T]ATGCTTTTAGGCAAA | 57630 |
| rs556300796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198941 | AGATAAAAACTGAGA[G/T]GATTTATTACCAGCA | 57630 |
| rs556333792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192657 | ACCCAAAGGAAAAGA[A/C]GTCATTATATGAAAA | 57630 |
| rs556375339 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169988 | ACTGTGCAAGAAATG[C/T]TACTGGAAAAAGTAA | 57630 |
| rs556395766 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133696 | GCAGGAGAATTGCTT[C/G]AACCCAGGAGACGGA | 57630 |
| rs556414316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134547 | CAAATGTTGCTAGGT[C/T]CCAAGATAAAAAGCA | 57630 |
| rs556472238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229530 | AGGACGTATACCATG[C/T]CTCTCTTTTAGAGGG | 57630 |
| rs556474871 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135090 | TTGTAATCCCACCAC[C/T]TTGGGAGGCCCAGGT | 57630 |
| rs556484127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170786 | TCTGTCTGATCTGTC[C/T]GAAATACAACTTTTA | 57630 |
| rs556492200 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149390 | TGGCAGAAGGAAAAG[C/G]AATAATTACTTGTAT | 57630 |
| rs556526486 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264601 | ATCTAGAATTCCCTA[A/C/T]CTTTCTTTCCCGATC | 57630 |
| rs556536935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161954 | GGAGGCTGAGACAGG[C/T]GGATCACTTAAGTCT | 57630 |
| rs556551557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142802 | TCCTCTCAGCAGACA[C/T]GAAAATATTTTGCCT | 57630 |
| rs556562614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239566 | ATAAAAAGGCATCAC[A/G]TTAAGGTTTCAAAAA | 57630 |
| rs556567999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230052 | CTCTACTATAAATAC[A/G]AAAATTAGCCAGGCG | 57630 |
| rs556578844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121312 | ACCAGAGATTATGTA[A/C]CCACTGGGAAAACTG | 57630 |
| rs556589828 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185877 | ACTACACAGCGTAAT[C/G]AAGAATCAAATGGGG | 57630 |
| rs556592240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170361 | TTTGTTAAGCATTTC[A/G]TGTATACTGCATAAG | 57630 |
| rs556595730 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123891 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 57630 |
| rs556623263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238524 | CTGTGAGGTAGGCAG[A/G]GCTGAGAATTATGAA | 57630 |
| rs556638393 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100796 | TTTACACAGCTGTAG[C/T]TACTACTATCACCAC | 57630 |
| rs556645584 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174012 | AGTTATATATATATA[C/T]ATATGGTGACTGAAT | 57630 |
| rs556646869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232098 | CAGGCATACAGGAAC[C/T]GGCTTAGAGCATTTT | 57630 |
| rs556648672 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185201 | GCACTGTGCTAAACA[C/T]TGAGGATAAAATGAA | 57630 |
| rs556686202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246485 | AGAGGTCATGCTTAA[C/T]GGCCAAAAAATTCAC | 57630 |
| rs556731143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269879 | AGAGCTGAAGGTTGA[C/T]AATTCTAAAAGACAC | 57630 |
| rs556739680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166211 | ATCCAGAATTAAAAT[A/G]ACTCCTACTAACCAA | 57630 |
| rs556764871 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111374 | ATCCTCCCACCTCAG[C/T]CTCCCAAGTAGCTAG | 57630 |
| rs556769401 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215788 | TTTGTTTTTTTTTTC[A/G]TTTGCTTGTTTGTAA | 57630 |
| rs556782809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170328 | AAGCAAGAGCCCATG[C/T]GTGCACCTGAGACTA | 57630 |
| rs556786193 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208408 | AAGGAAGCAGCAATG[C/G]GTAGGGGAGAAAAGA | 57630 |
| rs556790911 | snp | C/G | 1.99448e-05 | 0.00315784 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269252 | ATCTTCAGAAATGTT[C/G]ATAGTTGTGTGCATC | 57630 |
| rs556805405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222950 | AGCACCCCTGTCCTC[C/G]CATGGATTTTTATGA | 57630 |
| rs556810495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117136 | CTGTTTAAGATCCCA[C/T]AGGGTCCAAGGTAGA | 57630 |
| rs556832514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214819 | TATCCTTCAACCTTG[C/T]TAATTGACTAATAAG | 57630 |
| rs556834380 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203005 | GGATAGACAGCTCTT[A/G]GAGAAAAAAAGGTCT | 57630 |
| rs556863235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178942 | ATGTAAAACTCCTGC[C/T]AAATGCTGGAAGTCC | 57630 |
| rs556876544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139001 | CTGTTGCCCTGGCTG[A/C]AGTGCAGTGGCACAT | 57630 |
| rs556892278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145006 | AACCATCCAACCAAC[A/G]ACCCAGAAATGAAAA | 57630 |
| rs556924858 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094978 | CTGTGGTAAGGATCT[C/T]ATTCATTACCAGGCT | 57630 |
| rs556935063 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121351 | AAATGGCACTTGTTA[A/G]GCTTGAGAAGTAGCC | 57630 |
| rs556943957 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264469 | GGGGGACATAATTCA[G/T]CCCCTAACAGTCAGC | 57630 |
| rs557003301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262626 | GAGCTGAGATCTCAC[C/T]ATCGCCCTCCAGCCT | 57630 |
| rs557031353 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262985 | CAAACATGGTTTAGC[C/T]AAAACAAACAAACAA | 57630 |
| rs557046513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188218 | GTTACAGCACCCCTA[G/T]GAAACTCATACAGAA | 57630 |
| rs557047852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196777 | CTACCATTACAGAAA[A/G]CTCCTGGCCCTATGT | 57630 |
| rs557064355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261918 | AACAAAGAAAAATAC[G/T]ATGAGTATTTTTCTT | 57630 |
| rs557065866 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253760 | ATTTGCAAGCAGAGA[A/C]ATTATAAGGTGTTTG | 57630 |
| rs557071824 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114276 | ATTCCTTGACCTGTG[A/G]TCTCATTTCCCTATC | 57630 |
| rs557095906 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184547 | AAATTTAACAATGTA[A/G]TAGTATTCTGAAGAG | 57630 |
| rs557119284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174343 | GCAGGGATTATTGGC[A/G]TGAGCCATCATGCCA | 57630 |
| rs557131654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152384 | CAACCAGACTCTCCT[C/T]CATTCAAGCCTTGAA | 57630 |
| rs557141316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254651 | AGGCAAAGCATGAAC[C/G]AGCAACGTAGTGAGT | 57630 |
| rs557151832 | in-del | -/T | 0.251859 | 0.249993 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113111 | CAAGTCCCAGTTTTC[-/T]TTTTTTTTTTCCCCC | 57630 |
| rs557154212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225666 | CAGTCTGAGGAAATG[C/T]GGATGAGCCTACACT | 57630 |
| rs557156555 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160503 | CTGAAAATTCATTAA[A/T]TCACCCCAACTTGCT | 57630 |
| rs557165461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219399 | GTAACAAACTCCAGT[G/T]AGGTATATATTCACC | 57630 |
| rs557167473 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198985 | TGGAGCTTCTAAAGG[A/T]ATACTTTAAGGACAA | 57630 |
| rs557168310 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101991 | TAGTATACATTTCCT[A/G]TTTCCTTTATTTTTC | 57630 |
| rs557182989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190970 | GAATTAAAAACAAAA[A/G]TCACATCATCATCTC | 57630 |
| rs557198928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145479 | TCACCATGTGAGTGA[C/T]AGGTACATTAAAAGC | 57630 |
| rs557204105 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183060 | CCTGTAATCCCAGCA[C/G]TTTGGGAGTCTAAGG | 57630 |
| rs557220210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218805 | ACATGAATTAACTGA[C/T]TCATTAATGGAAAGA | 57630 |
| rs557221447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232924 | CTGCCTGGTTGTAAA[C/T]ATCAAGCCTTCGTAT | 57630 |
| rs557224980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227029 | AAACTAGCCAGGCGT[C/T]GGGGCACAAATCTCT | 57630 |
| rs557231571 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095473 | ATCCAGTAATACATG[C/G]AAGACGTGGGGAAAG | 57630 |
| rs557242185 | in-del | -/CGC | 0.0134861 | 0.0810011 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271018 | CGCGCACACACACCA[-/CGC]CGCCGCCGCCGCCGC | 57630 |
| rs557257409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182010 | TTTTATTTACTGCTG[C/T]ATCTTCAGGGTCTGG | 57630 |
| rs557280997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153956 | CACAATTCTATACTC[A/G]CCCAATAACAAAAAT | 57630 |
| rs557285295 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225885 | GAAAACAGAAGAGAT[A/G]AGCAGAGACATGTTA | 57630 |
| rs557303605 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134519 | TCTTTTATTTCAAGA[C/T]AACATCATTGTGCAA | 57630 |
| rs557310100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156331 | TTGCAAAAGGCAACA[A/C]GAGCTATATTTCTAT | 57630 |
| rs557335394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147300 | ACTATAAAAGAAATA[C/T]ACATGTATCTCAGGA | 57630 |
| rs557348695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232974 | GTAAACTGGGCCAAG[C/T]GCAGTGGCTCACACC | 57630 |
| rs557358292 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153195 | CTCTGGTACCCTCTG[C/T]GTGATAGTCTAATCT | 57630 |
| rs557372020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097071 | ATTTATTTGATTGGT[A/G]AGACTGGGAGAAGTA | 57630 |
| rs557373392 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203057 | TGAGAAGTTCTGCAG[C/T]AAAGAAACCTGTTTA | 57630 |
| rs557375986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103549 | CAGCATTGAGCACTT[C/T]TTATTGTGTTGAAAT | 57630 |
| rs557416776 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156070 | AAAATATGAAAGTAA[A/T]GACATTTCATTTTGT | 57630 |
| rs557432257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212343 | TGCCAGGATTACAGG[C/T]GTGAGCCACCGCGCC | 57630 |
| rs557435205 | snp | A/C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201062 | TGGCAAACAATAATA[A/C/T]AGTATTGTCACCATT | 57630 |
| rs557451548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118472 | TTAGTAGTAGTAGTA[A/T]TTTTTTTGAGACAGA | 57630 |
| rs557473938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239850 | ACATGGTGAAACCCC[A/G]TCTCTAATGAAAAAA | 57630 |
| rs557498411 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095559 | ACACGAGTGCATCAC[C/T]TACCACCACTATCTC | 57630 |
| rs557518717 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262780 | GAATCATTACTTTTT[A/T]AAAAAAATTATCAAT | 57630 |
| rs557550397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234638 | AGCTTTGGTAGAAAG[C/T]ACTGCCTGGCATTGT | 57630 |
| rs557574695 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111778 | GAAGAATAACAATGG[C/T]AGAAAAGGTCTAGGA | 57630 |
| rs557581930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261999 | TGAAGAAAAATTCTA[C/T]GAGTAAAAATACTAT | 57630 |
| rs557588588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189107 | AGAGATTCTTGTCAG[A/T]TCAAGTAGAAGCTTT | 57630 |
| rs557590166 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109953 | GGAGGTTGAAGTTGC[A/C]GTGAGCTATGACCAT | 57630 |
| rs557606029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131916 | TTCCCCAACTACTGA[C/T]TGTGGGCCAGCACTT | 57630 |
| rs557620359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226752 | GTATGCCAAAACTGT[C/T]AGTGAAGCTAAAGTC | 57630 |
| rs557630984 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164376 | CTAAAAAGATGATTC[-/T]ACTGACAGGCTCAAC | 57630 |
| rs557681439 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265587 | CAAGCGATTCTCCAG[C/G]CTTGGCCTCCTGAGT | 57630 |
| rs557707856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102765 | ACAAACACAGAAGAA[C/T]CCTTTTGTTCCTAAG | 57630 |
| rs557736092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166967 | GTGATATCTTCGACA[C/T]GGAAAAAGAGAAATG | 57630 |
| rs557782251 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140602 | ATGAGATGAAATACT[G/T]ACAAAAATAATATTA | 57630 |
| rs557783408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182322 | CACTCACAAAGGAGG[G/T]TGACCCAAAAATCAC | 57630 |
| rs557785030 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176683 | GTAGCTGAGATTACA[A/G]GCATGCACCACCATG | 57630 |
| rs557796072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255914 | CTGAGAGAGCAGGCA[C/T]GAGCCACCATGCCAA | 57630 |
| rs557844834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181443 | AATTTTTGTATTTTT[A/T]GTAGAGACGGGGTTT | 57630 |
| rs557854338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191085 | CCTCAATGTAATAAA[A/C]GCCATCTATGACAAA | 57630 |
| rs557856295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196482 | TGCTTTTGCAAAACT[A/G]TTAGTAGAAGTAATT | 57630 |
| rs557871086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241169 | CAGGAGGCGGAGATT[A/G]CAGTGAGCCGAGATC | 57630 |
| rs557872400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248141 | TCCCATTGGTGGATA[C/T]ATACCCAAAGGATTA | 57630 |
| rs557894660 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230331 | ACCCTCAAATAGAGC[C/T]GTGGATGCCCCATCC | 57630 |
| rs557935439 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248812 | AAGTGCACTGCTTAC[A/T]TTCAGTGACCTCATA | 57630 |
| rs557975530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118065 | CAAGACCAAATATCT[C/T]CACTGACTTTCAAGG | 57630 |
| rs557991884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146124 | TATATTCTATATATT[A/C]TATATATTATATATC | 57630 |
| rs558011517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154651 | AGTTAACCCTTATTT[A/G]TCCATCACACAGATA | 57630 |
| rs558024087 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221172 | TCAATAGCATTAAGA[C/T]GAAAGGCTGAACACA | 57630 |
| rs558032272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265351 | GGTCTCATGTGATCT[A/G]TTTTTTGGATGAATA | 57630 |
| rs558037705 | in-del | -/TATGGATTTAGAAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115178 | AAAAACCCCAAAAAC[-/TATGGATTTAGAAAA]TAATGTTTCCTTATA | 57630 |
| rs558040036 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108049 | TCTCTCTTTGGTCTG[C/T]TAGGAAAATCAGATG | 57630 |
| rs558051589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175098 | ACTGGGCTTCACCAT[G/T]ATGCCTCCGTTCCCA | 57630 |
| rs558101186 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097225 | TCCCTACGTCCCTTA[A/C]ACTGGTGTTTGACAT | 57630 |
| rs558113274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174695 | TCTCAACCCTGACTG[A/C]ATATTAGGATCAACT | 57630 |
| rs558139357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141468 | AGATCAAAGTGTAAG[C/T]TTAAAAATCGTTTTT | 57630 |
| rs558150045 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097566 | TGTAGGAAACGAGAG[G/T]GAGGTGACTTGTTTT | 57630 |
| rs558197621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259507 | CCTCTTGACTAGGCA[C/T]TGGCAGACATATACG | 57630 |
| rs558202511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133784 | CATCTCAAAAAAAAA[A/G]AAAAGAAAAGGAAAG | 57630 |
| rs558212342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140668 | TAAACTTTTTTGTGT[G/T]TATGGTTGCCCTCTT | 57630 |
| rs558229818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204742 | TTTTAGTAGAGACGG[A/G]GTTTCACCACTTTGG | 57630 |
| rs558233638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197560 | ACCCAGGAGGCAGAC[A/G]TTACAGTGAGCCAAG | 57630 |
| rs558256811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258733 | GCAAATGAAAACTTA[A/G]GGTCTGAAATCTAGT | 57630 |
| rs558273693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252288 | ACAGGACACAGAGTT[C/G]CTAAAATATTACTTC | 57630 |
| rs558279635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144254 | TGGGCAAGTCATTTG[A/G]CCTTGGGTATGCCTC | 57630 |
| rs558288410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161218 | CACTGCCAGCTTTAT[C/T]AAAAAGCTTGGCAAT | 57630 |
| rs558293084 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204106 | GAAAAAGAACTCAAG[A/G]GTAAGTAAAACTTCC | 57630 |
| rs558314976 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110633 | AAATGAATAAAAGAA[C/G]AATAGGAAAGGTCCT | 57630 |
| rs558319752 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127067 | ATTATGCAGAAGATA[A/C]GAGACTAAGATCTTC | 57630 |
| rs558322237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179818 | TCTACTTGAAACAGC[C/T]GGTTGGACTTTTCAA | 57630 |
| rs558324451 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124388 | TTTTGTAATAAAATA[C/T]AAAATCACTTCTTGT | 57630 |
| rs558337332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228571 | CTTCTAAAAGCCCCA[A/G]TGATTACACTGGACT | 57630 |
| rs558350967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157272 | GTCTACTCCTGGATA[C/T]AGCAGTGAGTGAACA | 57630 |
| rs558384110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187446 | TCCTGACTCAGTCTC[C/T]CAAAGTGCTGGGATT | 57630 |
| rs558388922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184243 | TTTCAGAAGAAATTA[C/T]CTACTGACTGCTTTG | 57630 |
| rs558400654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228003 | TATTAAGGATTTCAT[C/T]TCCTATAAAAGCAAC | 57630 |
| rs558410028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163822 | CTCCACCTCCCCACC[C/T]TGTATATGTATCACG | 57630 |
| rs558413920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150586 | CTCTTGAACTTACTC[C/T]TCCTACATAACTAAA | 57630 |
| rs558431082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103624 | GGCTTTTAATTAATC[A/G]AAAACTTTCATTCCC | 57630 |
| rs558436189 | in-del | -/T | 0.00159712 | 0.0282137 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142128 | GGCCTTAATTTGCAA[-/T]TTTTTTTAGTAGAGA | 57630 |
| rs558447968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191420 | AAATGGAAACACATC[A/C]CATGCTCATGACTGA | 57630 |
| rs558455391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114492 | AAGTTCCAGGGATCA[G/T]GAGGTGGACATCCTT | 57630 |
| rs558470052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234671 | GGAAACACCCTCATA[C/T]CATTTCCAATAGATC | 57630 |
| rs558503143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193388 | GAAAAGCTGCAGATG[C/T]GTTAGCTTCCAACAG | 57630 |
| rs558503517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209842 | TTGCCCAGGCTGGAG[C/T]GCAATGACACAATCA | 57630 |
| rs558507886 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246630 | CTGATGCATCTGCAC[A/G]TGCAATTAATTAGAA | 57630 |
| rs558526986 | in-del | -/TGA | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213324 | GTATATCTACTTTGG[-/TGA]AGTGTCTGTTCAGGT | 57630 |
| rs558571432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200635 | CATATGTATCATATG[C/T]ATTACTATGTGATAC | 57630 |
| rs558617415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245413 | TAGTCTACATATTTA[A/G]ATGTCCATGTTTCAA | 57630 |
| rs558630948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102051 | ACATTTTCATTTCTA[A/T]TCGCCCCTGGTATAG | 57630 |
| rs558644276 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239016 | TACCATGTCAGTCCT[C/G]TATTCACTCTCAAAA | 57630 |
| rs558655265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180417 | AATAATAACACTGTA[A/G]CTTAACACACTGCCA | 57630 |
| rs558655769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138067 | TAAAGACTTCTTCCG[A/G]TATGTGTTTAGGGAT | 57630 |
| rs558662469 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108222 | GAAACACTTCATAGA[G/T]AACTATTTCTTTAGA | 57630 |
| rs558686770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165578 | CCTGTAGTCCAATAT[A/T]GTGCCACTGCACTCC | 57630 |
| rs558717127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217698 | CCTGGGAGAAGGGAA[G/T]AGGGAGTTACTGTTT | 57630 |
| rs558717989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130401 | CAGTGTCTTACCTAC[A/G]GAATTCAACTGCCAT | 57630 |
| rs558738479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231517 | GTTGCAGTGAGCCGA[C/G]ATTGCACCACTGCTC | 57630 |
| rs558772435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224696 | CAGTAGCTGCAGGGG[A/T]AACCAGGAACAAGAC | 57630 |
| rs558773031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202805 | CTTAAACTTTGTACC[A/T]AAAGTAAAGCTTAAT | 57630 |
| rs558800437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231014 | GTGCTAAAATGTAAC[A/G]AAAAGGCCACCGGTG | 57630 |
| rs558830833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106523 | GCAATTAGTGGCAAC[A/G]GAATAGAAATAAGAA | 57630 |
| rs558836107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210431 | AAAATCTGAGTAAAT[A/G]CTAATTCTATAAATT | 57630 |
| rs558870829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195635 | AGTCCTTTTCTTCTC[C/T]ATATTTTCTTTTACA | 57630 |
| rs558886125 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218363 | TAAATATATATTATA[G/T]AATATATAGAATATA | 57630 |
| rs558894213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116901 | TTAGGAGACAGCCTC[C/T]CCACAGTGTTAGAGA | 57630 |
| rs558935953 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267877 | ATTGTTCTTTAAAAG[C/G]AGATTTTACCAGTTT | 57630 |
| rs558945403 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235961 | GCTGGGATTATAGGC[A/G]TGAGCCACCGTGCCT | 57630 |
| rs558982437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260384 | ACCGGCTCCCCACTG[C/T]GCCTCTTTTAGCCAC | 57630 |
| rs559007324 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269955 | AGTAGTTGATAAACT[C/G]TGAAACACATTTCTG | 57630 |
| rs559013124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151997 | AGGGTTAAAAATCTT[G/T]CCTTCTATTTTACAG | 57630 |
| rs559032670 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104566 | CTGGTTTTAGGGGGT[C/T]AGAACTATAGAAAAT | 57630 |
| rs559039786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171957 | TTTATATAATCATAA[C/T]ACTGCAAATGCTATT | 57630 |
| rs559076250 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150678 | ACATGCATCTTAGGG[A/C]CCCATGTCCGAGGAA | 57630 |
| rs559076565 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143197 | CACACTTGGAATTTA[G/T]ATTTTTTGGTAGCCA | 57630 |
| rs559079191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152475 | GGGTGCGGTGGCTCA[C/T]GCTTGTAATCCCAGC | 57630 |
| rs559087980 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154010 | ACAAACCAAGTATCA[A/G]CATGTAATATTGATA | 57630 |
| rs559114560 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166843 | ACACACCAGAAATTT[G/T]TCATTGCCACCTCAA | 57630 |
| rs559133548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187034 | AAAAAAATGAAAAAG[A/T]AAAAAAGAAAAGATT | 57630 |
| rs559140265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143668 | CATTTAAGCAGTAGG[A/G]CAGGGAGGAACACGG | 57630 |
| rs559151579 | in-del | -/CAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190974 | TAAAAACAAAAATCA[-/CAT]CATCATCTCAATAGA | 57630 |
| rs559182989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172020 | AGAATAGAATGTTAT[A/G]AACTCTGACAATATC | 57630 |
| rs559183279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164226 | GCATCTTTGTATCAT[G/T]AGTACCTACCTCAGT | 57630 |
| rs559190157 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122876 | GCTGGTAATCTTTAA[C/T]AAGTACACCAGTGAA | 57630 |
| rs559211532 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237114 | ATGTGGTGCCAACTG[G/T]CTGTGTGACATGCAC | 57630 |
| rs559228210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244748 | AAACACAATGACAAC[A/G]CCACAGTGCTGCACT | 57630 |
| rs559243989 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165993 | ACTCAAATGTAAAAG[C/G]TAAAACTGTAAGTTT | 57630 |
| rs559246491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158875 | GCCAAATTTGTTTTG[C/T]TAAACATTTGTTTAG | 57630 |
| rs559251591 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123378 | GACGCACGCTGTAAC[A/T]ATTCGATGCATTATG | 57630 |
| rs559257629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253921 | CTCAACTCAGCAGAA[C/T]ATTCTTTCTAATAAA | 57630 |
| rs559296163 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212066 | TCTTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 57630 |
| rs559307938 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095058 | CACCGTAATGAAATC[A/G]GTGGGAGAGGCCAAT | 57630 |
| rs559320525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261117 | CACAACCACTCTGCA[C/T]GGAGCTTAGGTCCCT | 57630 |
| rs559324215 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203887 | AAACAGATAGGGTTT[A/T]AAAGTCTGGTTGCAC | 57630 |
| rs559345069 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267548 | AAAAGAAAACCTCCC[A/T]ATCCCAGAGTTCTCA | 57630 |
| rs559348766 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231077 | AGCCCAAGTTTCTTC[A/C]TCTGTAAATAGAAGG | 57630 |
| rs559363818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202304 | TTACCTCCCTCCGTA[A/G]GAGGCTAGTTCTTGG | 57630 |
| rs559391133 | snp | A/G | 2.16424e-05 | 0.00328949 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122222 | TGTGGAGGCAAGGAC[A/G]GTGGCAGCCAGGAGA | 57630 |
| rs559409807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186493 | TAAAACATCCTGTTC[C/T]TTCAGGTGCAAAAAA | 57630 |
| rs559427283 | snp | A/C | 2.5228e-05 | 0.00355153 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130011 | CATGACTAAAGACCT[A/C]AAAGAGAAATAAAAA | 57630 |
| rs559478202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225421 | GAAAGAGGATCACCA[A/C]CAGAGAAAAGGCAGA | 57630 |
| rs559498360 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147938 | AGTGTGTATATAGCA[A/G]TAATAAAATATTTAA | 57630 |
| rs559499460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193593 | ATAGACATTTACCCC[A/G]TTACTAAGGATGCTA | 57630 |
| rs559501998 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138640 | AAACTATCAAATCTA[A/G]TTGATATCATGTTTA | 57630 |
| rs559511976 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117033 | TTTCTGTTTTTCTGA[G/T]AGAGTTCACAAGCCT | 57630 |
| rs559515797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115823 | AACACTTTTGATCAA[C/T]AGTTTCATCCCCCTC | 57630 |
| rs559543197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224958 | TAACAGGGTGCCCAA[C/G]GGTTTTATACTTTAA | 57630 |
| rs559553689 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257835 | TAATCCAAAGTCAGG[A/C]TCCCTAAACTGTCCT | 57630 |
| rs559559856 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145436 | AGAGGCAGGTGAAGG[C/T]TGAAAATTTACCTAT | 57630 |
| rs559573671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131370 | CCAGTTTCTTCCTTT[C/T]CTTCTTCTCCTCATT | 57630 |
| rs559617458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187091 | TTACACAAAAATACT[C/T]TTTTTGCTAACTCTT | 57630 |
| rs559618610 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266706 | CTGGGCTCAAGTGAT[C/T]CTCCGGCCCCAGCCT | 57630 |
| rs559629361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123848 | AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAA | 57630 |
| rs559655754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158450 | AACATAAAGGAGAGG[C/T]AGGCAGAGGCCAGTT | 57630 |
| rs559679555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107749 | TGAGCCTTATCATTT[A/G]CAGGCAGTGATCAGA | 57630 |
| rs559680546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224297 | CATATTGCCTATTTC[C/T]AGAAGGCCATGATCT | 57630 |
| rs559688875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198407 | CTGTAATTTTCCATA[A/G]GACTAGTCAATATAA | 57630 |
| rs559733754 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174982 | CGTGTCCAAAACAGA[A/C/T]CTCTTGGTTTCCACC | 57630 |
| rs559750074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205102 | ACAAGGGAGTGAAGG[G/T]AAATAGCTTCATTAA | 57630 |
| rs559757488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101053 | GCCTCCATGTATATG[A/T]CTTACAGCACTTAGC | 57630 |
| rs559782046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231770 | TCTACTTCTGTGTGA[A/G]CCATCTGTTTTCAAT | 57630 |
| rs559797525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246616 | CCTCCCAATCTTAGC[C/T]GATGCATCTGCACAT | 57630 |
| rs559810454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204575 | TTTTTTTTTTGAGAC[A/G]GAGTCTCATTTTGTC | 57630 |
| rs559815474 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230957 | AGTATAAACAATAGG[A/C]TCAAAAGGTTGAAAA | 57630 |
| rs559860044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246001 | AAACAGGAAAACACA[C/G]TCTGCCAGGGGTGTC | 57630 |
| rs559866503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139107 | TAGGTATGCAACACC[A/G]CACCCAGCTAATTTT | 57630 |
| rs559879098 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263183 | TAGTGAACCTTACAC[A/G]CCAGGGGAGCATGTC | 57630 |
| rs559879389 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228621 | CATCATCTCCTCTCC[A/G]GGTCAGCTGATTAGC | 57630 |
| rs559904941 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235427 | TTTAAGTCCCTTCCA[A/T]GATATGATAACTCTG | 57630 |
| rs559919833 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252645 | TCTTTAACCAACCTA[G/T]TCTATTTTTTTGGCT | 57630 |
| rs559924649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159112 | TCTGCTACTCTGCCT[C/T]GACCTAATCTTGTAA | 57630 |
| rs559935227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228499 | CATCTTCAACAGGAG[A/G]TTGAGTTCCTCATCA | 57630 |
| rs559943203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189239 | CAAAACACTTAAATT[A/C]AGAAAAAACTATCTG | 57630 |
| rs559966396 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248957 | TTAGGGACGGGCCCA[C/G]TGGCTCACGCCTATA | 57630 |
| rs559977855 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239899 | CGTGGTGGTGTGCAC[C/T]TATACTCCCAGCTAC | 57630 |
| rs559998344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235149 | GATATTCTTAAAATA[G/T]AATTCCTATAATCCT | 57630 |
| rs560007422 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221863 | ATCGTTACACAGTAC[A/G]AACAGTGAACTGCTA | 57630 |
| rs560029737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097371 | CAACATTACCAGTAA[C/T]GAGGTTGACATTCTC | 57630 |
| rs560076386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144546 | GAGACACATCTTTTC[C/T]GACTCATGATAAAAG | 57630 |
| rs560077290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185275 | TGAATGCAGGGAGAA[C/T]AGCCAAGAGAGAAAC | 57630 |
| rs560109249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257209 | CCAGCAGGAATCACA[C/G]AGCACACAAAAAAGG | 57630 |
| rs560110059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141732 | AACCTCTGCCTCCCC[A/G]ATTCAAGTGATTCTC | 57630 |
| rs560110598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235806 | AAGCCTCAGCCTCCT[C/G]AGTAGCTGGGATTAC | 57630 |
| rs560131804 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222994 | ACCCCTCGTGGTTTG[C/T]CCAGCTGCAGCTCTT | 57630 |
| rs560148883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111721 | GTCCAGATAAAGTTG[C/T]TATACTGATGACGGT | 57630 |
| rs560171608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242800 | TGATGCCTTCTGCCA[C/T]GTGATGATGCAGCAA | 57630 |
| rs560172029 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134038 | CATGCTCAATGCTCT[A/G]TTGTGGCCTGGGGTG | 57630 |
| rs560201390 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249694 | CACAGAGCAACAGTA[C/G]GAAGGATACATTTCC | 57630 |
| rs560205083 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149867 | ATTCTCAAGAGGAAA[C/G]GCTTTTAGTTAAAAA | 57630 |
| rs560220039 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220060 | GTTTTGCTGCAAAGA[A/T]ATACCAAAATTGTTT | 57630 |
| rs560245633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214936 | ATTTCTTCCTTCCCA[A/G]TCTTTATACCTTTTC | 57630 |
| rs560261992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256221 | TTTTCCCCAATCACA[A/G]GGAAGGAGGCAGAGA | 57630 |
| rs560262654 | in-del | -/A | 0.499995 | 0.00159744 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216997 | CTCTACAAAAATTAC[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs560269813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142110 | GGTGTGAGCCACTGC[A/G]CCTGGCCTTAATTTG | 57630 |
| rs560280481 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216813 | AAAGCAAAATACTAT[A/C]TAGTACCTCATGCAG | 57630 |
| rs560284751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265503 | TTTGAGATGGAGTTT[C/T]GCTCTTTTTGGCCAG | 57630 |
| rs560294011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111074 | GCACTTTGGGAGGCC[A/G]AGGCAGGGGGATCAC | 57630 |
| rs560313496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156975 | GAGGTTATCAGTATA[C/T]GAAAGCATGACTGCC | 57630 |
| rs560316140 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128313 | TCAGGGAAACCAAAT[A/T]TCACTAAAAGTTAAC | 57630 |
| rs560325465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255515 | GTATGGAAGTGAGGG[A/G]AAGGGTGGGCAAGGT | 57630 |
| rs560346253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106097 | ATATATGTGTGTGTG[C/T]ATATATATTTATTAT | 57630 |
| rs560360776 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200858 | GAGATGAGTAAACTG[A/G]TAAGTTTCTAGAGCT | 57630 |
| rs560372752 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125296 | CAGGGAAGAAGTGTC[C/T]TCTCTCTGAGTGGGC | 57630 |
| rs560376275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176204 | TATTTTGTCCTAGCA[A/G]CCCAAGATCCCTAAG | 57630 |
| rs560378101 | snp | C/T | 3.3442e-05 | 0.004089 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120802 | GAACATAGTAAACAA[C/T]GTATTCAAAACCATA | 57630 |
| rs560387311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181871 | AATCCCCTTATCCTG[C/T]TTTATTTCTCTTCAT | 57630 |
| rs560388297 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251162 | TCTGGGAGACACAAG[A/T]GGACAGAAGGTTAGT | 57630 |
| rs560403886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191798 | AGTGGGGGAGAAAAG[A/C]CTTTTTCAACAAATG | 57630 |
| rs560482288 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206516 | CGTCTCCATAAAAAA[A/T]TTTTAAAAATTATAT | 57630 |
| rs560484837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123367 | TCAAATTTCTAGACG[C/T]ACGCTGTAACTATTC | 57630 |
| rs560526131 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105508 | AAACAGGGCTTATTA[A/C]TCTGAGTGTAACTGA | 57630 |
| rs560527845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192343 | ATGAATAGACAGTTC[A/G]CAAAAGAAGATATAC | 57630 |
| rs560536283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162984 | AATCCAATCCACCAT[C/T]GCTAATGGAGTGTCT | 57630 |
| rs560566238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214198 | ATGAGTGAGCTCTCA[C/T]GAGATCTGGCTGTTT | 57630 |
| rs560582093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099519 | ATGATGTAGTTGCCA[C/T]GTGGGGCAAGTTAAA | 57630 |
| rs560592389 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177111 | AAGCACTGTTGGTTA[C/G]TTATATTTGATGGAT | 57630 |
| rs560601235 | in-del | -/A | 0.153332 | 0.230554 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233249 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs560617736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207412 | AGTCTAGGTGACTGA[C/G]TGAGACCCTGTCTCA | 57630 |
| rs560621449 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243978 | GCCAAAGTCAATATG[C/T]GAAGTCTGTCTCTAG | 57630 |
| rs560640164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192934 | TGATATATATATATA[C/T]GATGGAATACTACTC | 57630 |
| rs560657395 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273054 | CCATTTTCTTTTCTT[C/T]TCTTTTTTTTTTTTT | 57630 |
| rs560687139 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216483 | CTTTTATTGTTGTTG[G/T]GAGGATAAATAAAAT | 57630 |
| rs560687349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162821 | TTCCAGTTCCATACC[A/G]GCTCAAGAATGTGGG | 57630 |
| rs560745064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243794 | GAATCAGAATTATTT[A/G]TTTCTTCTATTTCAT | 57630 |
| rs560763921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199130 | GGGCAGCATGTAAAG[C/T]AGGAGAGAAGCAACT | 57630 |
| rs560818753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142238 | TGGCATTACAGGCGT[A/G]AGCGATTGCGCCTGG | 57630 |
| rs560823701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206198 | GATAAAACCTATGGA[A/G]TCTTCACTGCTATAA | 57630 |
| rs560865634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113134 | TTTCCCCCCTGAGAC[A/G]GAGTCTCACTCTGTT | 57630 |
| rs560883055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143018 | CTGAAGGGATTACTC[A/C]AGAGTCTTTTAAAAT | 57630 |
| rs560913526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178387 | TTATGTTTTGAGGCA[C/G]AGAATCACAGGGATT | 57630 |
| rs560936562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250219 | ATGAACACTGAAGTA[C/T]ACCAATGCTGTCAGT | 57630 |
| rs560942484 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135669 | AATAGTAAAGTGCTC[A/C]ATAAATGTCTGCCAA | 57630 |
| rs560950353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156226 | ATATAAGAAGTCTGT[C/G]CATAAAATTACCTTC | 57630 |
| rs560974093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215900 | CCTCAACCTCCTGAG[C/G]TCAAACAATCCTGCT | 57630 |
| rs560999691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249794 | GGCATATGACTGCAG[C/T]CATGTTTATGAGTGA | 57630 |
| rs561009222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236377 | GACTCTAATGACTAT[A/G]ATGAGCGGTGTCCCT | 57630 |
| rs561026940 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214885 | CTTTTGGATTTTCTA[C/T]GTATATTATCATGTC | 57630 |
| rs561046045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223568 | TGGGGGATACACCAC[A/G]ACACACCATGAATAA | 57630 |
| rs561053359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112972 | GAGATCAAATGATTA[C/T]TCTTAACAGGCTGAA | 57630 |
| rs561053563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169666 | TTTGTTTAAAGGTGA[A/G]AGAAGGAAGGAAGAT | 57630 |
| rs561118070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259041 | AAAACTAGATATGAA[A/G]CATCCTATAGCTAAC | 57630 |
| rs561149468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245615 | TACTTGGAGAAAACC[A/G]GATAATCCACCTATA | 57630 |
| rs561186879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177307 | TTTTCAGAAAACATA[A/G]ATCATTTTTCTAAAG | 57630 |
| rs561212135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143708 | ACAAGCCTCACTACA[C/T]CCTGCCAAGGGAAAA | 57630 |
| rs561213290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114141 | GCCGTAACAGGTTAA[C/T]TCAAACTTTGTGGTA | 57630 |
| rs561223160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229105 | GTAATATAATCATAC[G/T]TAAGAGTTTTGTTTT | 57630 |
| rs561228120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157538 | CTTTTCAACGGCATT[A/G]GGGGTGCCCAATCTT | 57630 |
| rs561234958 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167615 | CTGACACATGTGAGT[-/A]AAAAAAAATACTATA | 57630 |
| rs561249802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185365 | ACATAGCAAGGAAAA[A/G]GGAAGAATTCTAAAA | 57630 |
| rs561253191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170427 | CGAAAAATTTAAGAT[A/G]AGAAAATTAATAATC | 57630 |
| rs561298713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200053 | TAAAATGGACTCCAT[C/T]CAAAAAAAAGGAATA | 57630 |
| rs561321820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266301 | GAAGCAACATTCCAC[A/G]TTATCACTTTCAGCT | 57630 |
| rs561326860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251297 | TTCATTATATCTAAA[C/T]AAATACACGTAAAGT | 57630 |
| rs561328003 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237029 | GCACAAATATGCACA[C/T]GCTCCCTTCTCAATG | 57630 |
| rs561333698 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178260 | AGTAAACAAATAAAC[-/A]AAAAAAAAAAAATTT | 57630 |
| rs561354653 | snp | A/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137466 | GACAATAAGCTGCAT[A/G/T]TAACTTTCCCAGATA | 57630 |
| rs561361268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207477 | AATTTCTGGATATTA[C/T]ACCATTTGCTAAACC | 57630 |
| rs561370490 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123158 | TACCTAGTTAAGTGT[-/A]AAATGGCTTCTATAT | 57630 |
| rs561379826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219787 | TTCTTCATTTTTATC[C/T]CTCTACTACTTTCTC | 57630 |
| rs561385303 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265535 | CTGGAGTGCAAGGGT[A/G]CGATCTCAGCTCACT | 57630 |
| rs561387493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257978 | GGCAAATGTGAGAGC[C/T]ACATGTCACCTCAAT | 57630 |
| rs561395943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171051 | AAGTTTGACCTAAAG[A/G]TTTCTCCACACATAG | 57630 |
| rs561419179 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102493 | GATAAAGATGACTTG[C/T]TGTGTCTCCCTGAAC | 57630 |
| rs561424128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200967 | AGAAGTCTTCAGTGT[A/G]CTCTCGAGCCAGTCA | 57630 |
| rs561438441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218950 | TTACAGTATTTAGCA[C/G]TCAGACTTCTTAACA | 57630 |
| rs561451900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252001 | TATTTTTCAGTTGAA[A/G]CCTATAAAAGATAGG | 57630 |
| rs561455120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100838 | ACACTCCCCTAAGCC[C/T]GAACATGTCCCCTAT | 57630 |
| rs561489188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152783 | TCACTGTACCACCAT[C/T]GCTATTTTATCACCT | 57630 |
| rs561493616 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203165 | TGTTATTTAGTAAGC[C/G]ACACATTCACATAGC | 57630 |
| rs561495181 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266272 | ACCAAACACAGAACA[-/T]TAACTAATAAACTGA | 57630 |
| rs561512352 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122372 | TATAAATCCATAGAA[C/G]AAGACTTTAATGGAA | 57630 |
| rs561525107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102433 | GGAGATGAGCTTATA[C/G]GTATGTGGTTCTCAG | 57630 |
| rs561552633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248905 | CTCAGGTGTTGCCAA[C/T]GTGATGGTATTAAGA | 57630 |
| rs561568013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201691 | CATAATCATTTCCAT[C/G]GTAACTTCCTGTGAA | 57630 |
| rs561577341 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154405 | TACAGTTTGTCATTT[C/T]AGTTTTCAAGATCAT | 57630 |
| rs561586297 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261535 | ACATCCATGAAATAA[G/T]AATAATAATGTATAG | 57630 |
| rs561593197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252439 | TGACCATTGAAAAGG[A/G]CTATGAAAATTGCTA | 57630 |
| rs561618622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154299 | TGGTTTGAATTACTT[C/T]CCCATGGATATACAG | 57630 |
| rs561625211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157037 | AGCTTAACTTCCTAC[A/C]TTAACTACTTTATTC | 57630 |
| rs561644511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167956 | AGCCTAGACAAAATA[C/G]TGAGTCCCTGTCTCT | 57630 |
| rs561644606 | snp | A/C | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139111 | TATGCAACACCACAC[A/C]CAGCTAATTTTAGTA | 57630 |
| rs561654319 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103664 | TATAACATTTTCCTA[C/T]ATGTTACCGCACATT | 57630 |
| rs561666567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167122 | TGGTGCTCTAAATTT[C/T]TTAAGAACCTAATTA | 57630 |
| rs561675662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117836 | CAGCAAAATGACAGA[A/G]AGAACAATTAAATGC | 57630 |
| rs561689547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160780 | AGACTTATTCCCACA[A/C]AGACTGCAGATGATT | 57630 |
| rs561691767 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211923 | AAATTGCAAAAGTCA[A/C]TGTTACATGTTTTTT | 57630 |
| rs561718337 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262130 | GTAGGTCTATGTGCT[A/T]AAACATGAAGAGATT | 57630 |
| rs561728774 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271032 | CACGCCGCCGCCGCC[A/G]CCTCCCACTTTCCCA | 57630 |
| rs561744193 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240793 | ATGCTGCACTTGCCT[A/G]TTTTATTCATTACCA | 57630 |
| rs561749044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153501 | CCATTACTTAAGAAA[A/G]AGCCCCAGTTTTTAT | 57630 |
| rs561783595 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103014 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCATTTC | 57630 |
| rs561790758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173950 | CACTACCAAATACCT[A/G]ACTTTAAGGATACGG | 57630 |
| rs561794551 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133694 | AGGCAGGAGAATTGC[C/T]TGAACCCAGGAGACG | 57630 |
| rs561816696 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260483 | TCAACACAGGTTCTA[C/T]AGCAGCTGATGCAAA | 57630 |
| rs561830365 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137970 | GAAGTTTCTCCACAT[C/G]ATAATCATTCAGAAA | 57630 |
| rs561836144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160089 | GTGACAAATAACTCT[A/G]TTCACCATTATGGCC | 57630 |
| rs561894541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228232 | AAGTAGACCATCTAA[A/T]CACATTTCAGTAGAC | 57630 |
| rs561897527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140207 | ACATAAAGCAGCTTT[G/T]GCTGTAAGTATAGCA | 57630 |
| rs561900618 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186000 | TCCCCAGGAATCCTC[A/C]GAAACACTTAGGACA | 57630 |
| rs561921164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124604 | TTCCCAGTGCATGCA[C/T]GTTTGCATGTGTAAA | 57630 |
| rs561925649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184441 | GAAGTCAGTCAGACC[C/T]GGGCTTGCATCCAGG | 57630 |
| rs561933884 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218832 | AAGAAGCATTTAAGA[A/G]TAAAAAATGTTAAGT | 57630 |
| rs561944451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127214 | CTGTTACATGTGAAA[C/T]GTATGGGACAATGTT | 57630 |
| rs561945616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162100 | AGGCAGAGGTTGCAG[A/T]GAGCCAAGATGGCGC | 57630 |
| rs561973828 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254416 | ATGTAATAAACAAGG[-/TA]TATATGTGTTTAAGA | 57630 |
| rs562008397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161649 | GCTCCATAAAGTAAA[A/T]AAGATTCAGTGACCT | 57630 |
| rs562019594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203632 | ATTTCCTTCTGTAAG[C/T]GTATGGAATATTTAA | 57630 |
| rs562056058 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182754 | AAGTGTAAAGAACGA[C/T]ACACTGACTATCCAG | 57630 |
| rs562070569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168110 | GTGTCACTGCAGTCC[A/C]GCCTGGGCAACAGAG | 57630 |
| rs562103248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175386 | GGCTAACCTCTCTGG[C/G]TCCCTCTCCAATTCT | 57630 |
| rs562119480 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169313 | TTAAAAAAATAACAA[A/G]AGACTGGGTGCAGCA | 57630 |
| rs562131968 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119703 | TTCTGTCACCATCTG[A/C]AACAACAGTGATTTT | 57630 |
| rs562161261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132921 | ATCTATCTGATCTGG[C/T]GACCCACCTGGAAAG | 57630 |
| rs562163899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183414 | GCCTCCCGAGTAGCT[A/G]GGATTACAAGCACTT | 57630 |
| rs562170438 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212606 | TACAGAGAGTTCCCA[A/C/T]ATACTCCTAAACACA | 57630 |
| rs562198687 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234315 | CAAAAGAAACACCCT[A/C]CCCACCCCCCAAAAA | 57630 |
| rs562198923 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239947 | GAGAATCTCTTGAAC[G/T]CAGAAGTCAGAGGCT | 57630 |
| rs562245622 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152174 | ACAAGTGAAGAAAGG[A/G]CCTGTCTAAATTGAA | 57630 |
| rs562261983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263123 | AATACACATCCCCAT[C/T]CCCATCTGTGCGAAG | 57630 |
| rs562299397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256366 | ATAATGTTGCTCTCC[A/G]TTTCCTTTTACAGAT | 57630 |
| rs562334180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213346 | TCTGTTCAGGTCTTT[C/T]GCCCATTTTTCAATC | 57630 |
| rs562343443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242081 | TTGGTGGGAAAGGAG[C/G]GATCTATAAATTCTT | 57630 |
| rs562365047 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271562 | AGCCCTGGCGGGAAC[C/G]GATCCCGCTGCGCTT | 57630 |
| rs562366165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221388 | CAGATGACATGGGGT[C/T]GGAAGTACTTTTAAG | 57630 |
| rs562396203 | snp | C/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254954 | CACAGCCTGCAAGGT[C/G]AGGAAGAAGAGGTAC | 57630 |
| rs562419683 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101032 | ATGCTTGACTAAATC[A/G]CAGAGGCCTCCATGT | 57630 |
| rs562428842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154388 | AGTGCTGGCTACAAT[G/T]ATACAGTTTGTCATT | 57630 |
| rs562448453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126617 | TTTTTTTAGGAACAG[C/G]ATCTAGTCCTGGCTG | 57630 |
| rs562460371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103078 | GGTGCCCGCCACCGC[A/G]CCTGGCTATTTTTTT | 57630 |
| rs562471255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161514 | GATGAACTAGCTGAG[A/G]TTCTAACAGGTAAAT | 57630 |
| rs562497519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255333 | ACTGTTGCAGCATTT[C/G]CAAAATGCATCAGTA | 57630 |
| rs562500064 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191661 | ACTAAAGCCATAGTC[A/G]CCACAATAGCATGGT | 57630 |
| rs562519755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264265 | GTGGCATCTTCTCCA[C/T]GTGTCTTCACATGGT | 57630 |
| rs562520569 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191706 | AGCCACATAGACCAA[A/T]GGAACAGAATAGAGA | 57630 |
| rs562599549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118605 | GGAGTACAGGCACGC[A/G]CCACCATGCCCGGCT | 57630 |
| rs562650981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183567 | ATTACAGACGTGAGC[C/T]ACCATGCCCAGCCAA | 57630 |
| rs562680563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234946 | ACCCCATGACAAAAT[A/G]TCACCAGACATTACC | 57630 |
| rs562691271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222038 | TATCAAGTGTAGGTG[C/T]CTACTATGTAATAAT | 57630 |
| rs562706161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160826 | AACGACTTGGAAAAG[A/C]AATAAAAGAACACAT | 57630 |
| rs562717552 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272929 | AAGGGACAGTTTTTA[C/T]TGTGTTCTTATTTTG | 57630 |
| rs562753550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228741 | TCTGCCTACTGCAGC[A/G]TGGAATCATCCATCA | 57630 |
| rs562754138 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133949 | TCCTGTTTTAAATGG[A/T]CTTACATGAGCCATT | 57630 |
| rs562766432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153614 | AATTGAAGTCTGCCT[C/T]CACTTTATTCCCCTA | 57630 |
| rs562780424 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165922 | GAATAGATGGGGATG[A/T]ATCTTGAGCCCCTAC | 57630 |
| rs562792409 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257160 | CTGCCTGATAATAAA[A/T]CTCCTGCTTTTCCTA | 57630 |
| rs562803655 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197697 | AAACAAATTGTGTAC[A/C]GAATGATGTAATAAC | 57630 |
| rs562812699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127267 | GATTTAAAAATCTCA[A/G]TTCATGAAAAAAAGC | 57630 |
| rs562858126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264835 | TCCCTGTGGCTTGCC[C/T]AGTTCACACTTACCT | 57630 |
| rs562864554 | snp | G/T | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094141 | AGACATCTTCCGCTT[G/T]AGATGTATGCAAAGA | 57630 |
| rs562877000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128254 | GAGAGGTCATGATGG[G/T]TAAGGAAGTTGGCTC | 57630 |
| rs562903043 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220611 | CCCAATCCTGCCCCA[C/T]TTCCAGCAGTCTGGG | 57630 |
| rs562915971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221536 | AGTTCCGAGAAAAGT[C/T]TGAAAACATTAACAT | 57630 |
| rs562940433 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271852 | ATTGAGTCTGACCTC[A/G]GGTGGGCTGGCACCG | 57630 |
| rs562988034 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184619 | CTAATTAACTATGAG[C/G]CACTAAAAAGGAGAT | 57630 |
| rs562990348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105388 | TGGTAGCTATTTGTC[C/T]CATTAAATAATATAT | 57630 |
| rs563007845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162900 | GCACACACTCTGTGC[C/T]GTCTGCTGCCCTGCT | 57630 |
| rs563046166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207133 | TGGCTAACTTTTTTC[C/T]CTAAAGCAGAGACAA | 57630 |
| rs563116493 | in-del | -/A | 0.236724 | 0.249647 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217162 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs563121122 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115649 | TAATAATAGAAATAA[A/G]GTGCACAGTTAATGT | 57630 |
| rs563174924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214160 | GCACCTCTTATGAGT[A/G]GCTTGGTACTGTCCT | 57630 |
| rs563206710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165670 | AAGGCCTCAGTGAAA[C/T]TCAATTGCCTATTTT | 57630 |
| rs563221045 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130498 | ACAGCCTGGTGCTCA[A/G]CTAGCCTCCTAACAA | 57630 |
| rs563223970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231255 | ATGTTTGTTATCCCA[A/C]ATTTGTTACTCATAA | 57630 |
| rs563225306 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267513 | AGATCAGTTTCACAA[C/T]ATGTGGGCTCCAAAT | 57630 |
| rs563258382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224812 | CCATCAGGATTTGCC[C/T]AATGTGGCTTCACCT | 57630 |
| rs563300188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123622 | AGCTCGCAGGCGCAG[C/T]GGCTCACGCCTGTAA | 57630 |
| rs563302676 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176836 | TGAGCCACTGTACCT[A/G]GCCAATTTATATAGT | 57630 |
| rs563320536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231661 | ATTAGTTTTTGCTCA[A/T]AGCTGCTATAGAATA | 57630 |
| rs563330559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253471 | TATCACAGCTGGCTG[A/G]CTTATGATTTGAGAC | 57630 |
| rs563390772 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187609 | TTCCCTTTTTCACTA[C/G]AATAATCTCCAATAA | 57630 |
| rs563391031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260663 | CCAGCAGTAACAGAA[A/T]AATTTCTCTCCTTCA | 57630 |
| rs563402824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108619 | CTGATCCCCACCACC[C/G]TGCAACTCTCCCGGG | 57630 |
| rs563436216 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210841 | ACATCACTTTCCTCT[C/T]TCTGTCCACAAACCT | 57630 |
| rs563457613 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206766 | AAAATGACATGTAGC[A/G]TTGCATTCATTTTAC | 57630 |
| rs563476669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123075 | GAACCGCTACCTCGT[C/T]CTCTCCAGATCTTTG | 57630 |
| rs563482019 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094102 | AGAGGTAAAATGTGT[C/T]ATAATCACCAAATTG | 57630 |
| rs563491054 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219978 | TCAGTACAAACTAGC[A/G]TGTGGTACTCTAAAT | 57630 |
| rs563520298 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233824 | TTTCATTAAGAGACG[C/T]AATTGAAAATCTAGC | 57630 |
| rs563542777 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151462 | TTAGTAGTAGAGTCA[A/G]GATTGGAATCCTGGC | 57630 |
| rs563551283 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113128 | TTTTTTTTTCCCCCC[-/T]GAGACAGAGTCTCAC | 57630 |
| rs563562948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217839 | TTTAAAATGTTAAGT[A/C]TTATGCACATTTTAC | 57630 |
| rs563576905 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201661 | GTCAAAGTTATAATT[C/T]TGTATTCATAATACC | 57630 |
| rs563614914 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255029 | GAGTACATTGCAAGG[A/G]CAGGAATTTATGTTT | 57630 |
| rs563627396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172657 | GGTGTCAACTTGATC[A/G]GATTGAGGGATGCCT | 57630 |
| rs563634345 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229159 | CAGGATCTTGTTCTG[C/T]GGCCCAGGCTGGAGT | 57630 |
| rs563638705 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199613 | TGTGGCTTAGTGAAT[A/G]CGCAAAAAAAAAAAA | 57630 |
| rs563650418 | in-del | -/CGGGGACACAAATCCCT | 0.00755907 | 0.0610114 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270435 | CCCTTTAGCTCAGGC[-/CGGGGACACAAATCCCT]CGGGGACACAAATCC | 57630 |
| rs563656596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190288 | GAAACAAAAAGCTGG[C/T]TCTTTGAAAAGATAA | 57630 |
| rs563670666 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209081 | ATCACTTGAGGTCAG[A/C]AGTTCGAGACCAGCC | 57630 |
| rs563674591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240140 | AAAATAATCAACTTT[G/T]CAAAAGTCAATTAAA | 57630 |
| rs563680540 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132086 | TCTCTGCTTTTGTTG[C/G]TTCATTCTTTCCTTG | 57630 |
| rs563710647 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108589 | TTGACCTGGGCTATA[A/G]ATGAGCAGAGCCAGC | 57630 |
| rs563740639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196113 | AGCCACCACGCCCAG[C/T]GAACACAATAATTAT | 57630 |
| rs563750637 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120187 | CAAATGTTCCCTGGG[A/G]AGCAAAACTGCCCTC | 57630 |
| rs563753791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145195 | CCTGAGTGTCCATCA[A/G]CGGTCTACTGGATAA | 57630 |
| rs563806829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203004 | GGGATAGACAGCTCT[C/T]GGAGAAAAAAAGGTC | 57630 |
| rs563835412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254169 | AAGGATGTGAATGTG[C/T]TCCGATGGACCTTGG | 57630 |
| rs563849796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270189 | GCTGGGAGCATTAAC[A/G]GCTGTTCTTGACAAA | 57630 |
| rs563865805 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109268 | AAGCCACAGCTAAAG[C/G]TGTTTCTTAAAAGCT | 57630 |
| rs563867837 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101829 | GGCCTCTGCCTCTTG[A/G]TGGCTGTGTGACCTT | 57630 |
| rs563895367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159311 | TCTTCAAGGCTAGTT[A/G]TCACAGCTTAACAAC | 57630 |
| rs563898198 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174803 | TGGGTCAGAAGCATA[C/G/T]GGATTTTGAAAAGCT | 57630 |
| rs563928453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254729 | GGGTCCCATGACAGC[C/T]CTTCCACAACTTGAA | 57630 |
| rs563950697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131280 | TCTGTATCTATTAGT[C/G]TATATATTGATTGAA | 57630 |
| rs563987070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268407 | TTGATTTCCTATTTA[C/T]GATTTACCCACACAC | 57630 |
| rs564005397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224944 | CGAGTCTCATTCTGT[A/T]ACAGGGTGCCCAAGG | 57630 |
| rs564010957 | snp | C/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240639 | ACAGCATTTTTAATA[C/T]GTATACATTGTGAAA | 57630 |
| rs564019211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139162 | TATCTAGCTGGTGTC[A/G]AACTTCTGAGCTCAA | 57630 |
| rs564029632 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210030 | CAAACTCCTGAGCTC[A/T]AGCAATATGCCTGTC | 57630 |
| rs564030596 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095779 | TCTTTCTCATTGTTT[C/T]AGTCACTTCATTCTA | 57630 |
| rs564039294 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094552 | CAGGTAAAAAAATTA[C/T]CTTAACCTGTAGTAG | 57630 |
| rs564054020 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112755 | AGAATGAGCTTAAAC[C/T]TGCAAAAATGCTAAA | 57630 |
| rs564066211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173888 | GCTATTACCCTCTTT[C/T]TCACCAAGTCTTTTA | 57630 |
| rs564075935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124565 | GCTGAAACATAAATG[G/T]TTTAATACAATTGGG | 57630 |
| rs564076037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261414 | TAAAAGCAACATGAG[A/G]TCCCAGGGAAAATGT | 57630 |
| rs564085324 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266870 | CAGACTACTGAATAG[A/G]TTTGTTTTTGTCCTC | 57630 |
| rs564109483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269356 | ATGAGTGTTGTTATC[C/T]AGGGAAAAAGTTCAA | 57630 |
| rs564122807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182722 | TTGCAAGAAAACTTA[C/G]AGGAGGCAAAGTGTT | 57630 |
| rs564127460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172793 | TGCCAGCGCGGCTAG[A/G]ACAAAGCAAGCGAAG | 57630 |
| rs564136597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247676 | TTGTGGATCTTGCGA[C/T]CTGAGTCTGAGGAGG | 57630 |
| rs564140189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159997 | CATTTTAGATGTGGC[C/T]GTAGTTCATCTTGAC | 57630 |
| rs564185558 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102406 | ATAGATTTTTTTTTT[C/T]CCCCCAATTTAGGAG | 57630 |
| rs564247484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203459 | GGAAGGCTGAAGTGG[C/G]AGGATGGTTTGAGCC | 57630 |
| rs564259264 | snp | A/G | 3.69413e-05 | 0.00429759 | missense | SH3RF1 | GRCh38.p7 | 4:169116622 | GGCGTTCCTGGTTGT[A/G]CGCTGCAACTAGTAG | 57630 |
| rs564305162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203090 | GTTAAGAAAATGCTA[A/G]ACAAGCATTTTCCAA | 57630 |
| rs564328450 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263368 | TTGTGTGTTACCTCC[C/T]CCAAATGTAAACTTT | 57630 |
| rs564360657 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146503 | AAAGTGCTGGGATTA[A/C]AGGTGTGAGCCACCA | 57630 |
| rs564367856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211192 | AAAGAAGAAACTAGC[A/C]GGGCACGGTGTTGAG | 57630 |
| rs564368291 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228383 | CAAGGTGTTGGCAGC[A/G]CTGTGTTTTTTTTCT | 57630 |
| rs564375538 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234099 | CCCCTGAGAAAGCAG[C/T]GTCCTCATACAAATT | 57630 |
| rs564378157 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198083 | GGTCCAAATTATTGC[A/G]TCTAATGAGATTTTC | 57630 |
| rs564386522 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105084 | TCTGAAATACAGAGG[A/T]AAGGTGAATTTAAGG | 57630 |
| rs564490325 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166223 | AATGACTCCTACTAA[C/G]CAACAATTTGATTTA | 57630 |
| rs564522745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186315 | TTTACCTATGTAACC[C/T]GCACATACTGCACAT | 57630 |
| rs564543753 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126366 | TATCCTACTCTTCAC[C/G/T]CTGATTTTTAGATCT | 57630 |
| rs564545771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118256 | GTGGAAAGTCCTCTC[C/T]GTCTTCTCTTGACAT | 57630 |
| rs564554303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190374 | AATAAGCTCAATAAG[A/G]AACAAAACGAGAGAC | 57630 |
| rs564566196 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163829 | TCCCCACCTTGTATA[C/T]GTATCACGTGCCTGA | 57630 |
| rs564570599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240662 | TTGTGAAATTATATC[A/G]AGTTCATTAACATAT | 57630 |
| rs564583885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167280 | GATATATTATAATGC[A/G]TTCATTAGAATGATT | 57630 |
| rs564603608 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140827 | AGCTTCTGAGCACTA[C/T]AGGATACAAACAGTA | 57630 |
| rs564605075 | snp | A/T | 0.145978 | 0.227331 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219992 | CGTGTGGTACTCTAA[A/T]TTACAGGAAAGACAG | 57630 |
| rs564615772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197084 | TATCTCAGCTCACTA[C/T]AACTTCCACCTCCTG | 57630 |
| rs564646975 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095840 | AGGACTAGGTCTTCA[A/G]GGTGATTCCTACCAA | 57630 |
| rs564659186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212703 | ACCTACATTGACAAG[C/T]ATCATCAACCTAAGT | 57630 |
| rs564687649 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240783 | CACAGTCACCATGCT[A/G]CACTTGCCTGTTTTA | 57630 |
| rs564750643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227254 | CAAAAATCATTAGAC[A/T]ATAACATCAATCAAT | 57630 |
| rs564763095 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169270974 | CGCCGCGGCGGCACC[A/G]GGAGACTCCTCTCTG | 57630 |
| rs564769991 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182035 | GTCTGGAGCTATGCC[A/C]AGCACATAGTAGGCA | 57630 |
| rs564792330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179227 | GAGATGCAACTTTGC[C/T]GGCTTTGAAGACAAA | 57630 |
| rs564797011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243605 | CTCAGTTTAATCTTC[A/G]AACAGTATTTTAAGC | 57630 |
| rs564846634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132885 | CAGACACTCATGTCA[C/T]AGTCACAGACACTCA | 57630 |
| rs564851727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186999 | AGCCTGGGGACAGAG[C/T]GAGGCTCCATCGCAA | 57630 |
| rs564885633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129108 | CATCAGGACACACCA[A/G]TGGCATTCTCTGCAA | 57630 |
| rs564909307 | snp | C/T | 1.6517e-05 | 0.00287372 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136480 | GGAAGTGAAGGAGTG[C/T]CGCTTTTTGGTGTTC | 57630 |
| rs564942380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129840 | AGCTTCAGGCCACTG[A/G]TCCTCACTGTTAAAA | 57630 |
| rs564947756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223615 | TTGCTTGGAGCTTAC[C/T]TTCTTTTTTAAAAAT | 57630 |
| rs564967067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121858 | AAAGTTCAAACAGGA[A/G]TTGTACAAAAGAGGC | 57630 |
| rs564967143 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205696 | TAGCAGGACTAATAA[A/T]TTTCTCTTTCCCTTT | 57630 |
| rs564969872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268359 | TATTCATAAAACCAA[C/T]AGAATGATTCTAAGC | 57630 |
| rs564979060 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094290 | ATTTTAATCTTGAAA[A/C]CTTTTATCCAGTCCT | 57630 |
| rs565010532 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244272 | GTGCATGCACCCACC[A/T]CCATTTTTAAATTTT | 57630 |
| rs565017012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143091 | CTGTAAATATTTGTT[A/G]AATGAATAAAAATGT | 57630 |
| rs565036569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208032 | TAGACTCTACTTTGC[A/C]AGGCTTCCACATCTG | 57630 |
| rs565044799 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094998 | ATTACCAGGCTGTCT[G/T]CCCTCCTTTTGTTTT | 57630 |
| rs565049877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266425 | CTCACCTAAGGGAAG[C/T]GTCCAAAGAAGTGCC | 57630 |
| rs565053937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098713 | TGAGGAAGGAAGCAT[A/G]ACACAGCGGGAGAAA | 57630 |
| rs565055930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105959 | CGTGGGCATGCAGTG[A/C]AACACAAAATTCATA | 57630 |
| rs565075750 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157485 | AATTGTGTACATAAA[-/C]CCCAGTGCAATTTAA | 57630 |
| rs565078025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135754 | ACCTAAGAATAACGC[A/G]TGGCTATTTTTTACA | 57630 |
| rs565108101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142495 | TCTTTTCATTCTTTC[C/T]TTTTACATCTCCGTC | 57630 |
| rs565124930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252549 | TAATTAGCAACTCTG[A/C]CTGATTGCCAGATAA | 57630 |
| rs565142626 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238826 | TCTTCCTCCTCATAT[C/T]TAGCTCTGTCTTCCA | 57630 |
| rs565142695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231336 | ACTTTGGGGGGCCAA[G/T]GCAGGCAGATCACGA | 57630 |
| rs565197152 | snp | G/T | 1.69043e-05 | 0.00290721 | missense | SH3RF1 | GRCh38.p7 | 4:169106941 | GAACTGCGGAGTCCA[G/T]GGAACTTGCCTTCCT | 57630 |
| rs565205100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238115 | TGTATTCAGAATAGA[A/G]CCCTATCTCTGCCTC | 57630 |
| rs565216236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236948 | AGTAGAAGAGAGACG[A/G]TTGTATTTAACTGAC | 57630 |
| rs565218911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137829 | TGCTTCTACAGATGA[C/T]TGCAAATTGACTGAC | 57630 |
| rs565250456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209554 | ATATCTTGCTTGTAA[C/T]TGCAGTATTTTCAGT | 57630 |
| rs565254695 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175325 | CCTCCCACTTGAAAT[A/G]CAAACTCCTTCCTGT | 57630 |
| rs565288600 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234521 | AGAACATTTACATCT[A/G]AACAATGATATCCTA | 57630 |
| rs565377109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216917 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 57630 |
| rs565384755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178713 | GTAAAACCAGTCCAA[C/T]CAGGCCTAGACCATG | 57630 |
| rs565393616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259175 | GTTTTTTCTGGCAAA[A/T]AATAATAATAATAAT | 57630 |
| rs565399317 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132790 | TTATGAATCACTCCT[C/G]TGGAGGCCAAAAAAT | 57630 |
| rs565423258 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138245 | TTATAGTGGGAGTGG[C/T]CTGAACCTCACTGTA | 57630 |
| rs565428741 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217919 | TTGATCTAAGCCACT[-/G]GGTCTCTTCAATTTC | 57630 |
| rs565446718 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178968 | AGTCCAGGGAAAAAT[A/C]CATTGCATAGTAGAC | 57630 |
| rs565477582 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262155 | GAGATTTCATAGATA[C/T]AGTAAATGAATTAGC | 57630 |
| rs565504237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201148 | GATCAATATTTTTAA[A/C]ATTAACATCTTTAAA | 57630 |
| rs565521515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265661 | TATTTTTAGTAAAGA[C/T]GGGGTTTCACCATGT | 57630 |
| rs565532816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115736 | AAATCTGTCTTCAAC[A/G]AAACTGGTCCATGGT | 57630 |
| rs565579154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157169 | TAAAAATCAGAGTTC[A/G]GCTTTTAGGCAAATC | 57630 |
| rs565592363 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107608 | ATTTTAGGATAAAAT[A/G]GAAATTTCAGATTAT | 57630 |
| rs565603408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106370 | GTATATTTTCAGTGT[G/T]GCCCAAGACAATTCT | 57630 |
| rs565614919 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218253 | ATAATATAGAATATG[-/TT]TATATATAATATAGA | 57630 |
| rs565658391 | snp | A/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163143 | AGGAAAGTAGATAAA[A/G]TAGCTTTCTTACCAA | 57630 |
| rs565699985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223283 | AAATATAAGCCACCA[C/T]ACCTCTCCACAAAAT | 57630 |
| rs565745518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230828 | GCCATTGCACTCCAG[C/T]GTAGATGACAGAGTG | 57630 |
| rs565764653 | snp | G/T | 0.208169 | 0.246476 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229940 | GCCAGGCGAGGTGGC[G/T]CATGCCTGTAATCCC | 57630 |
| rs565766662 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112553 | CTCAAAAATGAAATT[C/T]TAACCATACAATTGC | 57630 |
| rs565769846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157878 | CCCAAGTAGCTGGGA[C/T]TGCAGGCAAGCACCA | 57630 |
| rs565815550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123331 | GTTCCAGAAACATAA[C/G]GAACTGAGTGGAAAA | 57630 |
| rs565840013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193806 | GTGATGAAAACAGAT[A/G]GAGTCTACGAGCCTT | 57630 |
| rs565877510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116097 | TGGGGTGGTGCCTGC[A/G]TTTCTTCCCCACTCT | 57630 |
| rs565897682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208167 | TTTTTTTTTTTTCCT[A/G]AAAGGAAACCACATT | 57630 |
| rs565913072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179705 | AACACTGCGCAAACT[G/T]TGAGTAAGTTCAATT | 57630 |
| rs565934143 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264734 | TTCCTATCTATCCTA[C/T]CCATCTGACCCTTCA | 57630 |
| rs565937817 | snp | C/G | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251590 | TTTCGTCCTTCAAAA[C/G]CTTTTAATGGACAGG | 57630 |
| rs565941127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129329 | CAAGGTCTTAAACAA[C/T]AGTCTTTCTCTACTA | 57630 |
| rs565948698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217582 | AACCTGAAAGGTGTA[C/T]AAGACAAGTTACTAA | 57630 |
| rs565956070 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121244 | TATCCCACCAAATAG[A/T]ATTTGCATAGTGTGA | 57630 |
| rs566002286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258482 | AAAAGAAAAATAAAA[C/G]TGCTACTATAGTACA | 57630 |
| rs566016968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224507 | ATTTTTAGTAGAGAC[A/G]GGGTTTTGCCATGTT | 57630 |
| rs566017648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121926 | ATCAGACTGATTTTC[C/T]TTCAGCAGTTCCCTA | 57630 |
| rs566019588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113440 | ATGACACCAAAGCAC[C/T]TTGCAGACCATCTGG | 57630 |
| rs566080058 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223968 | CAAAGAGGTAAGAGA[A/T]GTTGCTGGAAAGATA | 57630 |
| rs566100354 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124334 | AAAATCATCTATGCA[A/C]CTGATAAAAACATGT | 57630 |
| rs566184444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267775 | GGAACTAATGCTATC[C/T]CAATGGGCAGTTCCT | 57630 |
| rs566213990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245025 | CTGTAAGCGGATATT[C/T]CATCTTAATGATAGT | 57630 |
| rs566226771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197349 | AGCCCACCCAGCAGG[A/G]CGCAGAGGCTTACGA | 57630 |
| rs566231356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136941 | ATTTATTTCAGCTCA[C/T]TGTGAAATTTCGAGA | 57630 |
| rs566242184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150908 | ACAATCAAATAGCCT[A/G]GTTTTTAAAAAAACA | 57630 |
| rs566261697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100434 | ACAAACTCCGCCTCC[G/T]GGGTTCAAGCAATTT | 57630 |
| rs566264593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165205 | GAATCTGCCCTTCTC[C/T]TGCCACTGCCCTGCC | 57630 |
| rs566268177 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119215 | TTCAAGTGATTATCC[C/T]GCCTCAACCTCCAAA | 57630 |
| rs566278122 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171924 | GCTTCTTCTCCATCC[C/G]CACTGCAGTGAATCA | 57630 |
| rs566285551 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152635 | CCAGCTACTTGGGAG[A/G]CTGACGCAAGAGAAT | 57630 |
| rs566311720 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173678 | AGCCTAAATACCTTC[C/T]CTTAATTTGAGAGGG | 57630 |
| rs566319198 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096085 | CAAAACGAATCTCTT[A/G]CTCTCAACAGGAGAT | 57630 |
| rs566327835 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168586 | TGGAACTCGCTGAAT[-/A]AAAAAATACAGGCTT | 57630 |
| rs566327900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172167 | GCTGAAAACATATTA[C/T]TGAAGGCTTGGGTCA | 57630 |
| rs566352001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241477 | TTTTAATCCATCATC[C/T]ATGGAAGTAAAGGCC | 57630 |
| rs566358263 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133555 | GGCTGAAGTAGGTGG[A/C]TCACCTGAGGTCAGG | 57630 |
| rs566374513 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156067 | TATAAAATATGAAAG[C/T]AATGACATTTCATTT | 57630 |
| rs566377547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180235 | AAAAGGGATTACCCA[C/T]GAAGAATAAAGAGGT | 57630 |
| rs566410446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231364 | CGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 57630 |
| rs566432562 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158210 | GGTCTCTCGTGTTTG[G/T]TGAGTAGGAAAATGA | 57630 |
| rs566436009 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183232 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAAAGAGC | 57630 |
| rs566436768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183035 | CGGGGTGCGGGCATG[A/G]TGGTTCATGCCTGTA | 57630 |
| rs566474010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234495 | CATTTTGGTGAAGTT[C/T]GTTTGGGTGAAGAAC | 57630 |
| rs566476154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226828 | GCATTAGTCACCTAA[C/T]TCTAAATCTAAATTG | 57630 |
| rs566491451 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186229 | AGTGGTAGCTGGAAA[A/C]TGCCTGGACTTATTG | 57630 |
| rs566494059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148535 | CATTTCCTTTCCAAA[C/T]GTTCTGGAACATGAT | 57630 |
| rs566505789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221605 | AAACGTTCTTTATGA[C/T]AGCACTTCATTTTAA | 57630 |
| rs566532100 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271891 | GCTGAGAGGCGCCTC[G/T]TTTATCTGAGCCTGG | 57630 |
| rs566537846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103330 | ATGAATCCTACCTCA[C/T]AGTGTCCCAATAATA | 57630 |
| rs566553345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141905 | GCAAGTTCTGCCTCC[C/T]AGGTTCACGTCATTC | 57630 |
| rs566564448 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258633 | AAAACACAAGTTCAA[C/T]AATGGGGAAAAAACT | 57630 |
| rs566577920 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198391 | CTTCATGCTTAATAT[G/T]CTGTAATTTTCCATA | 57630 |
| rs566619648 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142558 | AGAATAAGGTCGGGA[A/G]AGCATTTAGCACTTT | 57630 |
| rs566636049 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154978 | CTGATTTAAAAAGGG[A/G]AAGGGGGCTAAGTAG | 57630 |
| rs566644088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255956 | TGTTTTTGGTAAAGA[C/T]GAGGTTTTGCTATGT | 57630 |
| rs566649850 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195598 | ATCCTTTAGGTCTCT[C/T]AACCTTTCTTCTATA | 57630 |
| rs566679813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220967 | AAGTTTAGCAGACAA[A/G]CAATTCTGGTTTAGT | 57630 |
| rs566722155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175689 | TATCATGACTAGGCA[A/C]CGACCCACCCAAAAC | 57630 |
| rs566773018 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130359 | TTACTAGATGCTGGG[G/T]AGTGATGTGATAAAT | 57630 |
| rs566783102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175106 | TCACCATGATGCCTC[C/T]GTTCCCATTCTTTCA | 57630 |
| rs566812794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162234 | CTACAAAGTAAAATA[C/T]CTGTCAAGATATAAT | 57630 |
| rs566838651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198751 | AAAGACAAAGAGAAG[A/G]CTTTACAAGAGAAAA | 57630 |
| rs566845402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213729 | GATTCATTGTTTGCA[A/T]TTGAATGTCCAGTTA | 57630 |
| rs566871030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098173 | CACTGACTTTTGGGC[A/G]TAACTGGTTACATGG | 57630 |
| rs566884621 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187375 | TTTTTTAACTTTTTG[A/T]GGAGATGGGGTCTCT | 57630 |
| rs566887971 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182518 | GGTATAGAAACTAAG[A/G]TAACATAAACCAACT | 57630 |
| rs566924271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185562 | CAAAGCTGGCATGGA[C/T]AGGAAAGTGAGATAA | 57630 |
| rs566933791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098814 | CTCTCAGTCTGTTTC[C/T]TCATCTGTAGAATAG | 57630 |
| rs566955299 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217013 | AAAAAAAAAAAAAAA[A/C]CCAGCCAGGTGTGGT | 57630 |
| rs566959524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236150 | CTACCATAAACATTA[C/T]GATTCTTCTCTCCCT | 57630 |
| rs566964674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204822 | CCAAAGCATTGGGAT[C/T]ACAGGCGTGAGCCAC | 57630 |
| rs566978933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161824 | CACAAAGAAATCATA[G/T]TAATAGAAAGTACCA | 57630 |
| rs566982477 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102396 | AAGATCATACATAGA[G/T]TTTTTTTTTTCCCCC | 57630 |
| rs566987600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192569 | CAACCACTATGGAAA[A/G]CAGCGTGGAGATTCC | 57630 |
| rs566993242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169139 | AAAGGAGCATTCTTC[C/T]AGTCAATTAAATGTG | 57630 |
| rs567022857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243042 | AAAGAACTCATTTCC[A/G]AGACAGCTGTCCAGT | 57630 |
| rs567055135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155866 | GATACCTACCCTAGC[C/T]TCCTGAGTTTGTTTT | 57630 |
| rs567056026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111445 | AATTTTTTTTTTTTT[A/G]GTAGAGATAGGGTTT | 57630 |
| rs567065675 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112686 | AGATCAAGAGAAGAG[A/C]CCATAACAAAGAACA | 57630 |
| rs567077610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104857 | AGTGAGCCAAGATTG[A/C]ACCACTGCACTCCAG | 57630 |
| rs567092675 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154850 | TACTATGAATTGTAA[A/C]TCCTTTATGTTCAGC | 57630 |
| rs567126355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184841 | ACCTAAACTGGACTA[A/G]GCAGTAGAAAACAGA | 57630 |
| rs567127220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104182 | CCATGCCAGTGCCTA[C/G]GGAGAGTCTGGGCAA | 57630 |
| rs567136846 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213830 | CACTTGACTATATTT[A/C]TGTGAGTCTATTTCT | 57630 |
| rs567138582 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206508 | TGAGACTCCGTCTCC[A/T]TAAAAAATTTTTAAA | 57630 |
| rs567155434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238767 | TCTGAAAACATTTCA[A/G]CTGCCCTAATATATT | 57630 |
| rs567175721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199452 | AATCTTGTGCATCCA[A/G]AGAGCAGAAGTGAAA | 57630 |
| rs567190676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242443 | TAGCTAAGATTTGCA[C/T]TTACATTTTGGATGT | 57630 |
| rs567210162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221648 | ATGCTCCTTATAACA[C/T]ACCTTGTAATCTATA | 57630 |
| rs567224359 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155694 | ACATGAATAAAAATG[C/T]TATGACATATCTTTA | 57630 |
| rs567224585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134125 | AGAAACCAGGCAGCA[C/T]TTCAAACACCTCCCA | 57630 |
| rs567236852 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271309 | CCCCCAGGGGACTAC[A/G]AGGGGAAGGCTCGGG | 57630 |
| rs567261921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119442 | TATACAAGCAGAGAG[A/G]CTTCTAATAATTGGT | 57630 |
| rs567266348 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177277 | TGCTTATCTTTCTGC[C/G]CTTCAATTTCAAATT | 57630 |
| rs567274879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191320 | AAAAAAAAAAACCTT[A/T]GGAATATACCTAACC | 57630 |
| rs567285354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142741 | CTTTGAAGAATATCA[C/G]GGAATGAATGAAATG | 57630 |
| rs567296950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184168 | CTTACTGTGAACCGA[C/T]ATCCCCTACTTCTGA | 57630 |
| rs567310334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243174 | TTCTCATTACAACTA[C/T]ACAATAAAAATACCA | 57630 |
| rs567344045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097486 | ATGGCAGAAGCTTAG[G/T]TGGTTTAATATTATC | 57630 |
| rs567347166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135027 | AACACGCAGTATAAA[A/T]CTAAAGGAGCAGGGT | 57630 |
| rs567386842 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123997 | TATCCTGTTAGGCTT[C/G]TTTCCAGTGACAAAG | 57630 |
| rs567397818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241528 | GGGTTGAGAGCATCT[G/T]GATGTGCTTTGGCGC | 57630 |
| rs567405697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205820 | AACCACAGATATAGA[C/T]ATGTACAAAACCCAT | 57630 |
| rs567434346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256627 | TTAGAGACAAGGTCT[A/C]ATTCTGTCACCCAGG | 57630 |
| rs567439896 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237869 | TAAATCAATTTATGA[-/T]TTCCCCCCCGCTCCA | 57630 |
| rs567459133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162356 | TGATTTGGCCATCAC[C/T]ACTAATGTTTCAACT | 57630 |
| rs567462904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176344 | CAATAATTTGAATGA[C/T]GGTACATTAGGGCAT | 57630 |
| rs567492446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141318 | TGAAATAATATTTCA[C/T]GAACATCTTTGCATA | 57630 |
| rs567502286 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104172 | GCTGCAGTGCCCATG[-/C]CAGTGCCTAGGGAGA | 57630 |
| rs567527681 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117350 | GGCTTGAAGTAATAC[A/G]CAGGGCACGCTTAGC | 57630 |
| rs567583310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168757 | AAAGGGACAGACTAT[A/G]ACTGATGATCTCTAG | 57630 |
| rs567586703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105631 | AGACATCGTGGCTCA[C/T]GCCTGTAATCGCAGC | 57630 |
| rs567628910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192601 | TAAAGAACTAAAAGT[A/G]GAATTACCATTTGAT | 57630 |
| rs567645333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243966 | TACCCTGGAGTTGCC[A/C]AAGTCAATATGTGAA | 57630 |
| rs567672823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257393 | CTGTTCGCCTCAGAC[A/C]GTCCTGACTTACTCC | 57630 |
| rs567699602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129387 | CCTTTTAATTTTCTT[C/T]CCAGAATGGCCCTCT | 57630 |
| rs567699842 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149117 | TGGGAACTCCATAAA[C/T]ATTAACCGATCTTTA | 57630 |
| rs567715741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247161 | TCAGACACTGAAACT[A/G]GAGATGGGGCCAGAA | 57630 |
| rs567739006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178879 | TGTAGTATGGAAGAG[A/T]TTTAGGTAATATCAA | 57630 |
| rs567745483 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145981 | ATATTCTATATATTA[G/T]TCTATATAAAATATT | 57630 |
| rs567759290 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230004 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGGTCA | 57630 |
| rs567798362 | snp | C/T | 1.76749e-05 | 0.00297273 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156399 | CAAGCACATTCTACC[C/T]TTACCTTTGCAAATG | 57630 |
| rs567805201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139436 | TGCTCCATGAGTCAG[C/T]AGTTCTTTCTTTTAA | 57630 |
| rs567820083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155927 | GAAAATAAACCAAAT[A/G]CCTACTCAAATGTAC | 57630 |
| rs567828643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236536 | TGTGACCTTAAACAA[A/G]TTATGTAACCTCTCT | 57630 |
| rs567831689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252879 | AGGATGGGTGGATTA[G/T]AGCAAAGGGGAAGTT | 57630 |
| rs567902160 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186644 | AAACTGAACTTAAAG[C/G]AGAGATTCCCATCAT | 57630 |
| rs567914202 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229480 | CCCCCCCACCCAAAA[A/C]AAAAACCTATTCGGT | 57630 |
| rs567915856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116724 | TGCATCAGACCATGA[C/T]GAAAGGCTGCTATTG | 57630 |
| rs567918124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098315 | TGAGTGTATAGCCTC[A/G]TGGGACCCACTCCTG | 57630 |
| rs567919533 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098982 | GAATGGGCCAGTCAG[C/T]GGCTGGACATCTCTA | 57630 |
| rs567963398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185677 | CCACAAGCCTGAGGA[A/G]GTTTTCAGACCCATA | 57630 |
| rs567974919 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236292 | AAGCTTTAAGCCAGA[A/G]CTCGACTTGCCAATT | 57630 |
| rs568047038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247965 | TCCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCT | 57630 |
| rs568060386 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095312 | AGTGCACTGAAGAGA[C/T]CTTGGTCAGTAGTGG | 57630 |
| rs568090016 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250107 | AATGTCACTTCTCTT[C/G]CTAAGAATATGTTAA | 57630 |
| rs568101135 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134973 | CCACAAAACAACAAT[C/T]CCACAATCCCATTCA | 57630 |
| rs568107730 | in-del | -/TC | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170275 | AATGACACATTTTTT[-/TC]TGTTTCTAGGTGATT | 57630 |
| rs568135974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158870 | TATAAGCCAAATTTG[C/T]TTTGCTAAACATTTG | 57630 |
| rs568138995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210208 | AGTCTTTCTGCTATT[C/T]TACCCTTCTCTCCTC | 57630 |
| rs568158932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270406 | CTCACCCTACAGCCT[C/T]CCTCATCTCCGCCTC | 57630 |
| rs568163825 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132890 | ACTCATGTCACAGTC[A/T]CAGACACTCATGAAC | 57630 |
| rs568166353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107998 | CTATTTCAATTCCAC[A/G]GAAGCCATCTCTTGA | 57630 |
| rs568167696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260939 | AAATAGAAATGAAAT[C/T]AAATATACAGCTAAG | 57630 |
| rs568168895 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166884 | TATCTGCAATGTAAA[A/C]ATCTCAAAACATCTT | 57630 |
| rs568186347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165772 | GTAAAAGATAGTTCA[C/T]AGTTTCAGAATTAAA | 57630 |
| rs568199631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151788 | GAGTGGGCGATATTT[C/T]AAACAAATGACTAGG | 57630 |
| rs568216656 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226710 | TTGTAGATAATAAAA[C/T]CTATCTTTGTAAATC | 57630 |
| rs568238577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232050 | TTTCTGGTTAGGTAG[A/G]CAGGTACTGCAGGAC | 57630 |
| rs568278437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190794 | CTACAGACCAATATC[C/T]CTGATGAACACAGAT | 57630 |
| rs568279748 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223343 | CATTCTATGAGAGTT[C/T]TGAGGCACTGGCAAG | 57630 |
| rs568283216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159389 | ACAGAGAGAGAGAGA[G/T]AGAGAGAGAGAAAGA | 57630 |
| rs568299796 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239493 | GTCCATATGTATGTA[A/T]GTTTTTATTAAAATA | 57630 |
| rs568367588 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196291 | GAAACTGTGGCTTTA[A/C]GTAAAACACCATAAA | 57630 |
| rs568367790 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103184 | CTCGTGATCCACCCA[C/T]CTTGGCCTCCCAAAG | 57630 |
| rs568423222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262540 | GGCATGGCGGTAGGC[A/G]CCTGTAATCCCAGCT | 57630 |
| rs568425882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160472 | GTTAGCCTAGGGTTA[C/G]ATTTCCGTGATGCAA | 57630 |
| rs568463749 | in-del | -/AC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255626 | CATACACACATACAC[-/AC]ACACACACACACACA | 57630 |
| rs568547023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196330 | AATTTTTTCTTATCA[A/G]CATTACAATGAAACA | 57630 |
| rs568552264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226493 | GCCTGATTTAAAGAA[A/C]AAAAAAAAAGAGCAA | 57630 |
| rs568553088 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178210 | TGCGCCAGCATGCTC[A/C]AGCCTGGGAGACAGA | 57630 |
| rs568555916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174302 | CTTAAGACTCAAGCA[A/G]TCCTCCCGCCTCAGC | 57630 |
| rs568574461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096914 | GATGGCCCAGACTGG[A/T]TCATCTGAGTGACCT | 57630 |
| rs568589381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146707 | GAGAGCAGGGGTAAG[C/T]GATTCTCTTGAGAAG | 57630 |
| rs568599660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133034 | GCCCTTTGGCTTCCA[A/G]CTTGTCCCTTTCACC | 57630 |
| rs568626784 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096796 | GGAAATAACATTAAT[A/T]CATTTATGATTGTAA | 57630 |
| rs568648013 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187106 | CTTTTTGCTAACTCT[G/T]AAATTATTAGAGCAA | 57630 |
| rs568652069 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145134 | AGAAACCTGTACTTG[C/T]ACGTTTATTGCAGCA | 57630 |
| rs568660456 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241085 | AATACAAAAAATTAG[A/C]CAAGCGTGGTGGCGG | 57630 |
| rs568662492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249044 | CATTCTGGCTAACTC[A/G]GTGAAACCCCATCTC | 57630 |
| rs568698532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270608 | CCATCCGGGAAGCAG[C/G]GGGTGCTGGGCTGCG | 57630 |
| rs568702782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102031 | TGGTGTTCTCTGTAG[C/T]TCATACATTTTCATT | 57630 |
| rs568717377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146822 | GATCATTTTCCTATA[C/T]TAAAGGATAGCCAGG | 57630 |
| rs568748937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248460 | CATGGATACAGGGAG[A/G]GGAACATCACACACC | 57630 |
| rs568752549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255153 | TTTCTAAAAACCCAG[C/T]AGATGACCATTTTCA | 57630 |
| rs568760993 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131575 | GCAGGAGAATAGGGT[C/G]TGAAGGCAGGGAACC | 57630 |
| rs568793466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139636 | GGACATAAGCTCCCA[C/T]CTGGATATTGGGTAC | 57630 |
| rs568807830 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131627 | CCCAGAACTAAACTG[-/A]AAAAGAAAACCTTAA | 57630 |
| rs568811437 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118364 | AGATCTTATGATTCT[A/G]TTGTTTCATGTGGAT | 57630 |
| rs568813471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109754 | GTGGCTCACACCTGT[A/T]ATTCTAGCACTTTGG | 57630 |
| rs568842310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232932 | TTGTAAATATCAAGC[C/T]TTCGTATGCAGCAGA | 57630 |
| rs568842323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240897 | CAAGCATCCCCCTCA[C/T]TGCAAGGAAGCCTTT | 57630 |
| rs568857313 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159240 | GGGAAAGAAGAATTC[C/T]AATTTTTCTCTACCC | 57630 |
| rs568871024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196437 | GACAATGTTAGGTAA[C/T]GATGTACTATATTTT | 57630 |
| rs568931441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203237 | ATCTTGCTCTTTGTA[C/G]TTGAAAGAGCAAATA | 57630 |
| rs568943231 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155635 | ACCATTAAGCTTGTC[A/G]TTTAATTTTCCTTTT | 57630 |
| rs568945978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254522 | TAGTGGCCAATTGCT[A/G]ACACTATCGTAAAGA | 57630 |
| rs568973227 | in-del | -/TAAA | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189076 | AAGATAGTTTGGGCT[-/TAAA]TAGTTATTCTGAAGA | 57630 |
| rs569010579 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271085 | GAGGAGGAGGCCGGG[A/G]CGCAGCCGGCGCCCG | 57630 |
| rs569017213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175066 | CCCACTGTTCACCTC[A/G]TTGCTTGGGCCAAAA | 57630 |
| rs569025735 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162545 | AATCATTTTCTTAAT[C/T]TTCTACCTCCCACCT | 57630 |
| rs569037805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226698 | TATAGGAAACTATTG[C/T]AGATAATAAAACCTA | 57630 |
| rs569085453 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220598 | GATTTTAGCAATTCC[C/T]AATCCTGCCCCACTT | 57630 |
| rs569116365 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126708 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 57630 |
| rs569125513 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247563 | GAACAAAGTAGCATC[A/G]CTTGATAAATGGTAA | 57630 |
| rs569150799 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153339 | AAAAAAAGCAAAATA[C/G]CTAACACTGATGGAG | 57630 |
| rs569182852 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182102 | GACTTAAGTGGAAGA[A/G]TGGAATAGAATATTT | 57630 |
| rs569208506 | in-del | -/TAG | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146011 | ACATATTCTATATAT[-/TAG]TCTATATAAAATATT | 57630 |
| rs569210704 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255807 | GAGTCTCGTTCTGTT[G/T]CCCAGGCTAGAGTGC | 57630 |
| rs569230783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220796 | GAATGTGAAATTACA[C/T]GGAAATGCAATCCGG | 57630 |
| rs569235962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204711 | ATGCACTACCACGCC[C/T]GGCTAATTTTTTGTA | 57630 |
| rs569261810 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156222 | TTTCATATAAGAAGT[C/G]TGTGCATAAAATTAC | 57630 |
| rs569265840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147870 | GACTTAACATTTGAT[C/T]AATTAAAATGAATCT | 57630 |
| rs569266625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104104 | CCGGAATGCAGAAGC[C/T]GTAGAGACTGAGGAC | 57630 |
| rs569269271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175600 | ATTATCCCACAATAG[C/T]CTCAACCCAACCAGC | 57630 |
| rs569296757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212869 | CTCATTCTCCCTGCC[C/T]CTTAACTTCTGGCAA | 57630 |
| rs569341563 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123462 | AAAGTGGTTGCAGAA[A/C]ATTTAGTGCAGAAAC | 57630 |
| rs569351417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266783 | GAGTGCCACAGTACC[C/T]GGCTCGAAAAACTAT | 57630 |
| rs569353127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167721 | GAGGTGGGCAAATGA[A/G]TGAAAGAGGGTGTGA | 57630 |
| rs569358488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212353 | ACAGGCGTGAGCCAC[C/T]GCGCCTGGACTATTT | 57630 |
| rs569365883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163785 | CCTCCACCAAAATTC[A/G]TCGAGAACAGTCCAT | 57630 |
| rs569369896 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174756 | TTTTCTAAAGCCCCA[C/T]CCCAAACCAATTAAA | 57630 |
| rs569373772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220205 | AATTTTGACTGCTTT[A/G]ATAATGAAATTTAAA | 57630 |
| rs569401665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249893 | AATTCATCTCTGACA[C/T]TAATCATCAGGCTCC | 57630 |
| rs569464697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256449 | CCAGAACTATCTTAT[A/G]TAGTCACTAATTTAT | 57630 |
| rs569471647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191360 | AAAGACCTCTACCAG[A/G]GAAACTACAAAACGC | 57630 |
| rs569496439 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241513 | AAGTAAAGGCCTTAG[A/G]GGTTGAGAGCATCTG | 57630 |
| rs569497576 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183565 | GGATTACAGACGTGA[A/G]CCACCATGCCCAGCC | 57630 |
| rs569506748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110494 | AATAAGCCAGGTGCC[A/G]TGGTGTGAACCTGTA | 57630 |
| rs569511683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208279 | CTGCCCTTCCACCCA[C/T]TTTATCTTCTATAGG | 57630 |
| rs569527609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259405 | CCTTCCCAGCTACCC[C/T]GAAAGAGCCCACTCA | 57630 |
| rs569531643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197964 | GTTCATACACTTGCT[C/T]AGACTGCCAAATACA | 57630 |
| rs569549435 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193984 | TCTCAAGGATAGAGT[A/C]TTTTTTTCATGTTTG | 57630 |
| rs569569056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205421 | GTAGTAATAAGCATG[A/G]CAACTCTCCCAAGTG | 57630 |
| rs569623209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157215 | TTTTAATGTGGGCAG[C/T]AGGTCTTACTCTTTC | 57630 |
| rs569669246 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093782 | TGATAAGTCATTTGA[C/T]AGTAGCCAAAAGTTA | 57630 |
| rs569686511 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171557 | ATAGGAGAAAAGTAG[A/T]CAGCAGAAAAAAGGC | 57630 |
| rs569692970 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216306 | TGGAAATTATAATGT[A/T]TTAGAAATTATAATT | 57630 |
| rs569708206 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223893 | AACCCTGGGGCAGAA[C/G]AGTTGGGCATATTTA | 57630 |
| rs569730644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151572 | TCCCTTAGATGAGGT[C/G]AGAGAAAGTCTGTCA | 57630 |
| rs569738373 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192786 | ATATATATATACATA[C/T]ATGTTTCTTTTATAT | 57630 |
| rs569749366 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179383 | CCTGTGTTAGACTTC[G/T]GACCTACAAAAGTAT | 57630 |
| rs569756795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188576 | CTCCCCTTATTTACA[A/G]TATAAAAGCTAATGA | 57630 |
| rs569760159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121968 | GACCAGGTAGAAGTT[C/T]GCAGGACACAGACCG | 57630 |
| rs569763654 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101300 | GGAATGAAATTCTGA[C/T]ACGTGCTACAACAGG | 57630 |
| rs569771374 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230670 | TCAAGACCAGCCTGG[A/C]CAACATGGTGAAACT | 57630 |
| rs569798115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194388 | CAAAATGCAACCACA[A/G]TCATGGCTTTTGCCT | 57630 |
| rs569806712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223465 | AGTTAAGAAAAGAGA[A/G]GGAAACCAGAGCATG | 57630 |
| rs569813286 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253261 | AATCTGCCATTCTTC[C/T]TAATCCATAAGGAAA | 57630 |
| rs569818325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187885 | TTCGCAGATGGAATC[C/T]GCAAAGTTAAAATGA | 57630 |
| rs569831385 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172454 | TTCATATCAGCATTT[-/A]AAATGTCATTAACTT | 57630 |
| rs569853285 | in-del | -/ATATAATATAAT | 0.0123036 | 0.0774623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218197 | GTGTAATATATGTAA[-/ATATAATATAAT]ATATAATATAATATA | 57630 |
| rs569854250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246263 | CATGAGACACGTATT[C/T]CATAAAGAGAGCTCA | 57630 |
| rs569858571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237610 | TCTCCAGCTGAATCA[C/T]AGGTACAGTAAACAA | 57630 |
| rs569877356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211414 | ATGAACCCGGGAGGC[A/G]GAGCTTGTAGTGAGC | 57630 |
| rs569888066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252685 | AGTATGTCTAGTAAT[A/G]CTGCCAAGAAACGAT | 57630 |
| rs569903175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122337 | ACATCTTCCTATGGA[A/C]GGTGGGAGAGAAAAA | 57630 |
| rs569928661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219117 | TTTCCCAACTCACAA[A/G]AAAATTACAATGAGG | 57630 |
| rs569936817 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187980 | GACATCAGAGTGAAG[A/G]AGGCTGGGTGGTGAG | 57630 |
| rs569950487 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260119 | GAGGTGTGCAAAGGA[C/G]AGCTGGGGGCTCGTG | 57630 |
| rs569973881 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225834 | AATCCAGTGGAGAGA[C/T]TGAAGTTGCAGGATG | 57630 |
| rs569998784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115302 | TGTGAGGAACCAGGC[C/T]GCACAGCAGGAGGTG | 57630 |
| rs570000508 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218315 | TAAATATAGAATATA[G/T]AATATAGAATACAGA | 57630 |
| rs570017875 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231434 | AGCCAGACGTCATGG[A/C]GCATGGCTGTAATCC | 57630 |
| rs570030245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268056 | ACCTATATTTCTAAT[A/G]AATACAGATTATTTA | 57630 |
| rs570035976 | in-del | -/TGT | 0.0292472 | 0.117338 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176932 | GTTAATTTCTGTTGT[-/TGT]TGTTGTTGTTGTTGT | 57630 |
| rs570083269 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117366 | CAGGGCACGCTTAGC[A/C]CAAATAAGCAGATAC | 57630 |
| rs570112907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202751 | AAAAAGAAAACCTAA[A/C]CCCTTTGAATCCCTT | 57630 |
| rs570127417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253885 | ACATATCACATATTT[C/T]AACTTTTATAAGGCT | 57630 |
| rs570128036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239268 | GAATATTTTTGTAAC[C/T]ATTGCATATCTCTAT | 57630 |
| rs570141568 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166423 | AAATCCTATCCTTAT[G/T]AGAGGAATTGGCAGA | 57630 |
| rs570170329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159509 | AACTCCAGAGCCAGA[C/T]TGCAGGGTGTGAATC | 57630 |
| rs570190390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238296 | CAGGGAGAAAGGAAC[C/T]ACCTACCAGGTGTCA | 57630 |
| rs570204233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145222 | ATAAAGAAAATGTGA[C/T]ATAAATGCAACAAAG | 57630 |
| rs570225926 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094689 | TTCCTAACTAAAGTT[C/T]ATTTCACCAAACCTT | 57630 |
| rs570237555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259517 | AGGCATTGGCAGACA[A/T]ATACGCGACAAAAGG | 57630 |
| rs570241132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261564 | AGTGAGCCGTAAACA[C/G]TCCAACTGCACTCCA | 57630 |
| rs570266835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140045 | TTTGTTAGCAAGATG[A/C]TGTCATACTTTAAAA | 57630 |
| rs570298375 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123352 | GAGTGGAAAAAAATT[G/T]CAAATTTCTAGACGC | 57630 |
| rs570300037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261087 | CAAACTCAGCCCCCT[C/T]ACCAGCCCCATTCCC | 57630 |
| rs570322102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123243 | GTCATCTTATTTCTG[C/T]TTTTTGGAATAAAAA | 57630 |
| rs570331487 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170539 | AATTGTTTAACTAAA[-/T]TTTTTTTAGGCAAAG | 57630 |
| rs570349989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138502 | AAATCTTTGAAAGTG[A/C]AAACCTAATCAGTGT | 57630 |
| rs570355143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157946 | GTCTCGCCATGTTGG[C/T]CAGGCTGGTCTCAAA | 57630 |
| rs570364503 | snp | C/G/T | 0.000338424 | 0.0130041 | missense | SH3RF1 | GRCh38.p7 | 4:169268848 | CTCCAGGATTGCACC[C/G/T]GAGGCTGCTGTCCGC | 57630 |
| rs570380904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144776 | ATTTTTTTTTTTAAG[A/G]AAAGCTTATGTAAAA | 57630 |
| rs570422411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202033 | CCATCTGCAAAATGA[A/G]AAAGTATCTCATAAT | 57630 |
| rs570447725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253565 | TTCTCAATAATTTTA[A/G]TTTAATTTTGAATGT | 57630 |
| rs570459476 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139863 | CAGCTTCCTAATCTA[C/T]AAAGTAAGTTGGAGC | 57630 |
| rs570532956 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221646 | CTATGCTCCTTATAA[C/T]ATACCTTGTAATCTA | 57630 |
| rs570544492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208387 | AAGAAAGTCTTGTAA[C/T]AGGCAAAGGAAGCAG | 57630 |
| rs570566617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115392 | TTACTGCCTGAGCTC[C/T]GCCTCCTGTCAGATC | 57630 |
| rs570569651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224467 | GGATTACAGGCTCGC[A/G]CCACCATGCCTGGCT | 57630 |
| rs570577385 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095233 | CTGCTGGGAGGACAT[A/G]AAAGACCACTTTCAC | 57630 |
| rs570580572 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182574 | TTTTATTAGTCTCTA[C/T]CACAGACTAATTTGG | 57630 |
| rs570583578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172140 | ATACTGTATGAGCCT[A/G]AGAAAGCAAGAGCTG | 57630 |
| rs570592015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187965 | ATGTGAAAACACAGA[A/G]ACATCAGAGTGAAGA | 57630 |
| rs570596974 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248739 | GGAACTTGGAGCTGT[G/T]CACCTGGTGGGTGTT | 57630 |
| rs570623384 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181025 | GCTGTATTCTTTTCT[A/T]AGTAAAATAGATGAA | 57630 |
| rs570626259 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228080 | ATTCTACTTTTTCAG[A/C]TGTTTCCAGGAACAG | 57630 |
| rs570626841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238382 | AGCCATCTTCACCTT[C/G]AGGAAAATGAATATT | 57630 |
| rs570637180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102575 | CTTTTATTTGCCATC[C/T]CTTCTGAAATATTTT | 57630 |
| rs570654179 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103805 | ATATTTAATATTCCA[C/T]TGAACATATGGATTA | 57630 |
| rs570680084 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196587 | ACTGTAGAATCACCT[A/T]AATCTAATTTCAGGG | 57630 |
| rs570687039 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246394 | ATATTATCACTGAAG[A/T]ATCAAACTGAGCTAG | 57630 |
| rs570716326 | in-del | -/T | 0.301681 | 0.2446 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106008 | GAATTTTTTTTGCAA[-/T]TTTTTTTTTAGCTCA | 57630 |
| rs570741471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166010 | AAAACTGTAAGTTTT[A/G]TAGGGGAAACAAGAA | 57630 |
| rs570753346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202543 | ACCTTCAGCTTACAG[C/G]TAGCTTATAATTAGT | 57630 |
| rs570759944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107888 | ATCCATTTTAAGGAA[A/C]GCTTCAGTATATTTA | 57630 |
| rs570767713 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158509 | GAGTTTTTATTGCTG[C/T]GTTCTTCTGGTAATG | 57630 |
| rs570774431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218379 | AATATATAGAATATA[A/G]AATATATATATTATA | 57630 |
| rs570781359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219144 | GAGGAGCTGATAGAC[A/G]CAAGCATAAGAACAG | 57630 |
| rs570808119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269744 | CCCTTTTTTAAGCCA[C/T]TTTAGCGTTTAAGAA | 57630 |
| rs570856513 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219060 | CTCCTTAATAACCCT[A/T]TCTTACATAACAGAG | 57630 |
| rs570860224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161035 | TTTCCAAACTGCTGC[G/T]TTTCTTCTGTATCCT | 57630 |
| rs570865896 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210899 | CTCAACCTATTCTGG[C/T]TCAGGGACTTCCCGA | 57630 |
| rs570871672 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176786 | CCTCAGGCAATCCAC[A/C]CGCCTCAGCCTCCCA | 57630 |
| rs570877594 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127800 | ATTTACTACATTGTA[C/T]AATTTTCAGCCCACA | 57630 |
| rs570938900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225125 | ACCAAGACAAGGTTA[A/G]TGCCAGTTAATGACC | 57630 |
| rs570940827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232712 | CTAAATAAAATGGGA[A/G]TTGATTGGGTAAATT | 57630 |
| rs570953678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176469 | TCAATTTTAACCGAA[C/G]AAAACAAATATTAAT | 57630 |
| rs570955595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185447 | ACAAAACAAACAAAC[A/T]AACAAAAAACCCACA | 57630 |
| rs570956235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248151 | GGATATATACCCAAA[A/G]GATTATAAATCATTC | 57630 |
| rs570960034 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192863 | TATCATATAGATGTG[-/AT]ATATATATATCATAT | 57630 |
| rs570961296 | snp | A/C | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153027 | CTACAGGTCCACAAT[A/C]CTACCCCAAGGCCCA | 57630 |
| rs570979134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138684 | GTCAAACAATAGACT[A/C]CATTAGTGGTGCTTG | 57630 |
| rs571016957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184935 | TTCCAACTCTAGGTC[C/T]CTCACCTTAGTTTTC | 57630 |
| rs571067966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207571 | GAATCAACAATACCC[A/T]AAGAAGAACTGCCAA | 57630 |
| rs571096945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116908 | ACAGCCTCTCCACAG[C/T]GTTAGAGACACTGAG | 57630 |
| rs571107684 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118205 | CCACATCACACATGT[C/G]CCCATGTACATGCAT | 57630 |
| rs571118452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106660 | ACCCATTAAGAAACA[A/C]GGAAGGAAAAAGGAA | 57630 |
| rs571119666 | in-del | -/AATCAAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192466 | TGCAAGAATGGCCAC[-/AATCAAAA]AATCAAAAAATAGTA | 57630 |
| rs571120387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262469 | GTCAGGAGTTGGAGA[C/T]CAGCCTGGCCAACAT | 57630 |
| rs571120455 | in-del | -/T | 0.0142736 | 0.0832652 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101653 | TATGAATGAATAAAA[-/T]TTTTTTGTTTAAAAA | 57630 |
| rs571120656 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254574 | GGAGGGTAGTAAAAA[C/G]TAACCACTCGAGAGA | 57630 |
| rs571130736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206702 | GCATCAAAGGTCTAA[C/T]CTTTATAGGGTGCAC | 57630 |
| rs571158480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229387 | ATATAATACTTTATT[A/G]TACAACACATGATGT | 57630 |
| rs571166763 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121059 | TGCTCAAAATTCTTC[A/C]TTGGTACAAAGTGTT | 57630 |
| rs571191970 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214497 | TGATTGGGATTGTGT[G/T]GAATCTATAGATCAA | 57630 |
| rs571201801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124860 | CAGTTTGCTGTCCTG[C/T]AAGACCTGAAATTTC | 57630 |
| rs571209812 | in-del | -/AGA | 0.00636936 | 0.0560724 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206165 | ATCACAACTCTCAAG[-/AGA]ACATTAGGAAAATAT | 57630 |
| rs571236971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235014 | CATTGAGAATCACTG[C/T]TTTAGAGGGTTTTTT | 57630 |
| rs571268867 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272546 | AGACGACGGAAGGAA[C/T]GAATGGAATGGAGAA | 57630 |
| rs571288552 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215868 | GGGTGCAGTGGTGCA[A/G]TCATGGCTCACTGCA | 57630 |
| rs571299900 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268656 | TTATATCCAATCTCA[C/T]TCCAAGATGGGGGAA | 57630 |
| rs571355141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114259 | TTCTAGAGGCTTCCT[A/G]TATTCCTTGACCTGT | 57630 |
| rs571378550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199648 | ATAAATAACAGAGGA[A/G]ACTAATACATTTTTG | 57630 |
| rs571385763 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152891 | GAGGGCAAACTATTC[C/T]GGTAGCATTTCTCAC | 57630 |
| rs571391939 | snp | A/C/T | 0.000921416 | 0.0214447 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130161 | CTTATATGAACCTGC[A/C/T]GAGAAAAGAAAAGTT | 57630 |
| rs571394522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235498 | AACTGAAGCACAGAA[C/T]GGTTAAGTAACTTGC | 57630 |
| rs571416988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250755 | CAGACATAAGTGCCA[G/T]GAAGAAAAACAAAGC | 57630 |
| rs571429674 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099181 | CACTGTAGCCTTGAC[C/T]TCCCAGGCTTAACTG | 57630 |
| rs571441519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215336 | TAATTCTTTTATACA[C/T]TGTTGCATTTGATTT | 57630 |
| rs571487505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134221 | TATGGAAGGAGGGGT[A/G]GAATGGTTGAAGGGG | 57630 |
| rs571504069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106281 | CCACGTCTATTTCTT[C/T]GTATTTTAGTAGAGA | 57630 |
| rs571516954 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150936 | ACAGGAAAAAAGCTT[G/T]CATTAAGGTCACATA | 57630 |
| rs571526874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257484 | AGGATAAACGACATG[G/T]TCGCTCTGTCTAAAC | 57630 |
| rs571528864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265583 | GGTTCAAGCGATTCT[C/T]CAGCCTTGGCCTCCT | 57630 |
| rs571528879 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197458 | TTGTGAAACCCCGTC[C/T]CTACTAAAAACACAA | 57630 |
| rs571551008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127643 | GTTTAATCAACCTTC[C/T]TCTTGCTTAACATGC | 57630 |
| rs571560341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099766 | TTTGAACTAGAACTG[C/T]TGCTGGGCTAAGAAC | 57630 |
| rs571567715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120263 | ATATTATAGAATTCA[C/T]TGTCAGAATTCAGAG | 57630 |
| rs571575759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143829 | TCTGTTGGCCCTAGC[C/T]GTTAAAAACAAAATA | 57630 |
| rs571585738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172203 | CCAGGTAAAAAGCCA[C/T]GACCAGCTCAGTTGC | 57630 |
| rs571636326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136770 | TCCCATGTGAGATAT[C/T]TCTTCTCTCAATATT | 57630 |
| rs571636924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237324 | GACTTTCACCAGGTG[C/T]TTATTTACCTGGGGG | 57630 |
| rs571636978 | snp | A/G | 0.207559 | 0.246371 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230059 | ATAAATACAAAAATT[A/G]GCCAGGCGTGGTGGT | 57630 |
| rs571648497 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143413 | GTTTGGACGAGTCTC[A/G]CTGCAAGTTGCTCAA | 57630 |
| rs571821337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169371 | GGAGGCTGAGGCAGG[C/T]GGATCATATGAGGTC | 57630 |
| rs571837242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157099 | TGATAGATACTGAGG[A/G]GAAAAATTTAAACCA | 57630 |
| rs571886033 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257912 | GGCTCCTGTGGCAGG[-/CA]CAGTGTGGGCTTCTA | 57630 |
| rs571901642 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170391 | GAAGGTAACAGATCA[C/T]GCTAGCTGTATTCCT | 57630 |
| rs571914343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179602 | GAAGAACTTCCCACT[C/T]TCTTCAGGTTATATA | 57630 |
| rs571941067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192738 | TGAAACCAACCCAAA[C/T]AGCCATCAACAAATG | 57630 |
| rs571962232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206931 | GAAGCCAAGAGTTCA[A/G]TACTGGCATGAACAA | 57630 |
| rs571982657 | snp | C/T | 0.000165033 | 0.00908236 | missense | SH3RF1 | GRCh38.p7 | 4:169156652 | CATAGTTGTATAATG[C/T]TTTGGCACATGGTAA | 57630 |
| rs571996568 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192322 | AATGATCAGGGAAAT[G/T]CAAACATGAATAGAC | 57630 |
| rs571997321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162665 | AAATTAAGACAAAAC[A/G]TTGTTTCTTCATTCA | 57630 |
| rs572000788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199706 | TTCCAATCCACTGGG[A/C]ATAAGAAAACAAACA | 57630 |
| rs572007441 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133642 | AACTAGCCGGGTGTG[G/T]TGGTGGCGCCTGTAA | 57630 |
| rs572009939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105807 | GGGAGGATCACTTGA[A/G]CCCAGGATGTTGAGG | 57630 |
| rs572023782 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168138 | GAGTGAGACCTCACC[G/T]CTAAAAACAAAAACA | 57630 |
| rs572024084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214110 | CCTCAATGTTGGAGG[C/T]GGGGCCTCGAGGGAA | 57630 |
| rs572044958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148703 | GGTACTGTAGAAGTT[C/T]AAAGCAAGGAGAGGG | 57630 |
| rs572049275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250160 | ATAAAAAAGCATTCC[C/T]TTCCATGCTCTCATT | 57630 |
| rs572079339 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099290 | GATGGCATCTCACTA[G/T]ATTGCCCAGGCTGGT | 57630 |
| rs572091371 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198396 | TGCTTAATATGCTGT[A/T]ATTTTCCATAGGACT | 57630 |
| rs572110705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149736 | TTTAAAGGAAAATAA[C/T]ACATCTAAAGGAAAA | 57630 |
| rs572113139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256767 | ATGCCCAGCTAATTT[A/T]AAAAAAAAATTTAGA | 57630 |
| rs572126245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114612 | CTGTTCTTATCAGTG[A/G]CAAGGGCTCTGAGAC | 57630 |
| rs572141047 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112185 | ACGAGGAAAGATAGA[A/G]ATAATGAGGGCGTTA | 57630 |
| rs572145509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213305 | ATCTTTTCATATGCC[A/C]TATGTATATCTACTT | 57630 |
| rs572146069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236362 | GCTGGGTCTCTGAGT[A/G]ACTCTAATGACTATA | 57630 |
| rs572154084 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118587 | AAGCCTCCCGAGTAG[C/T]TGGGAGTACAGGCAC | 57630 |
| rs572173615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142927 | GTTTTTGTTTTTGGA[A/T]GACCTAAATATAAAA | 57630 |
| rs572181644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222999 | TCGTGGTTTGCCCAG[C/T]TGCAGCTCTTCACAA | 57630 |
| rs572207403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243393 | CAGCGCATGCCTGTA[A/G]TCCCAGCTACTCAGG | 57630 |
| rs572218535 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105996 | TTAAAATATTGTGAA[-/T]TTTTTTTTGCAATTT | 57630 |
| rs572219527 | in-del | -/AG/AGT | 0.480461 | 0.0968913 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157921 | ATTTTTGTATTTTTA[-/AG/AGT]CAAAATGGGGTCTCG | 57630 |
| rs572224893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119564 | CATTATTATCATTAT[G/T]TTGCACCAGGGAGGT | 57630 |
| rs572257243 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180368 | TGATCCTCCACCTCA[C/T]TGAATTGTTGACATT | 57630 |
| rs572262755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156185 | GAAAATGATACCACA[C/T]AGAGCATCAACCAAG | 57630 |
| rs572291263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105264 | GATGACACTTAAGAC[A/G]AATACTATATATTTA | 57630 |
| rs572328008 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241211 | CTCCAGCCTGGGCGA[C/T]AGAGCGAGACTCCGT | 57630 |
| rs572346051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107523 | GAAGTAGGATAAACC[A/G]ATAAAAAAGATGTAA | 57630 |
| rs572347578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251925 | CTTGCATATTCATCA[A/T]TCAAAACTATATTTT | 57630 |
| rs572350408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112900 | AAGGATAATCTTCAG[A/C]CTGGAGGGGAAGAAC | 57630 |
| rs572364770 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144702 | CACTATAGTGAACTA[C/T]GGTCAACTGGGGACT | 57630 |
| rs572391712 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250890 | ACTGAAGGAAAGGAG[A/C]AAGCCATGTTGAGAC | 57630 |
| rs572429200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106786 | AAATATCACAATAAT[A/G]TTCCAGCCTAAAGCC | 57630 |
| rs572446471 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177448 | TGCAAGAACAGAAAC[-/A]AAGAGCTATTATAAA | 57630 |
| rs572448825 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178272 | AAACAAAAAAAAAAA[A/T]TTTTTTTTTAAATAA | 57630 |
| rs572456633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125333 | TCAGAACACTGGCAG[A/G]TGACAATGCTAGTGA | 57630 |
| rs572493177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100188 | TTATATGAACAGGGG[C/T]TTGGGGAAGTTCTGA | 57630 |
| rs572503929 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186868 | AAAAAAAAAAAATTA[C/G]CGGGGCGTGGTGGCG | 57630 |
| rs572514113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158028 | ATAGGCATGAGCCAT[C/T]GCACCCAGTGCAAGC | 57630 |
| rs572536843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236809 | TATTCCCATAATAAA[A/T]TGCTACATATGTAGG | 57630 |
| rs572544622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107408 | ACTGGTTATTCATAA[C/T]CTGGCCACCAAGTTT | 57630 |
| rs572576349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225337 | AACCAGAGCTCCAGC[A/G]CAAGTGAGGGCTGGA | 57630 |
| rs572580906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128967 | TCTGTGAAGTAGATA[A/C]TTATTTTATGGCTAG | 57630 |
| rs572599282 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118946 | GTTTTGTGTAATGTG[-/T]TTTTTTTCCATATTC | 57630 |
| rs572627180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136260 | TGAGCAAACATGTTT[A/G]TAAGTTGATCCTTTT | 57630 |
| rs572689206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215863 | GGCTGGGGTGCAGTG[C/G]TGCAATCATGGCTCA | 57630 |
| rs572690464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129580 | AAACAGCCACAGCTA[C/T]AGACCATATGGACAC | 57630 |
| rs572730042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164487 | TCCATCTTTTTGAAA[C/T]TGTCCTCCCAAGTAC | 57630 |
| rs572746706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254746 | TTCCACAACTTGAAG[C/T]CCCATTCAGAACTTT | 57630 |
| rs572766280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269977 | ACATTTCTGAACGGC[A/C]TGTCCTAATCCCATT | 57630 |
| rs572793726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124576 | AATGGTTTAATACAA[C/T]TGGGCAGATCTTTTC | 57630 |
| rs572850363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174750 | TTAAAGTTTTCTAAA[A/G]CCCCACCCCAAACCA | 57630 |
| rs572865070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141477 | TGTAAGTTTAAAAAT[C/T]GTTTTTTGAAGTAAC | 57630 |
| rs572884416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240558 | ATTTAAAGATACCAA[C/T]GTGTATTAAGGAGTT | 57630 |
| rs572889696 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147865 | GACATGACTTAACAT[G/T]TGATTAATTAAAATG | 57630 |
| rs572890890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110705 | GTCATTGGGAATTTG[G/T]GGGCGGGGGATTTGA | 57630 |
| rs572915610 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173892 | TTACCCTCTTTCTCA[A/C]CAAGTCTTTTAGAAA | 57630 |
| rs572941262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102956 | AGATGGAGTCTCGCT[C/T]TGTCAGGCTGGATGG | 57630 |
| rs572959283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249223 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAGAAA | 57630 |
| rs572983946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139726 | ATCATGTGTATGCAG[A/G]TAGACACATCCTGGA | 57630 |
| rs572998062 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262781 | AATCATTACTTTTTT[A/T]AAAAAATTATCAATT | 57630 |
| rs573024306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132002 | GGCCTGAGAAGACTC[A/G]GTATCCAGGGCCCTT | 57630 |
| rs573027388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204195 | GATGAAAACAGAGTT[A/G]CTTTCTAAAGACTGC | 57630 |
| rs573037034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220350 | TTTCATTTTAAATAC[A/G]TGTTCCTTCGCAAGT | 57630 |
| rs573042778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132611 | CCTGAGTTTCTGCTG[G/T]GCTTACCCTTTTCTC | 57630 |
| rs573061623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270703 | TGCTCCGCTTCCGCA[C/G]GTCCTGATTCCCGGC | 57630 |
| rs573071091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211878 | CATCTCTTGGAGAGG[C/G]GGCTTTTCAATGTAA | 57630 |
| rs573090706 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203512 | GCTGAGATGGCACCA[C/T]TGCACTCCAGCCTGG | 57630 |
| rs573100990 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124668 | AGAAACTCTGATTAA[A/T]ATCAGATTCCTAGAT | 57630 |
| rs573124336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167777 | ATTCTGTATCTTGAC[A/G]GAGGTGTTAGTTATC | 57630 |
| rs573138086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219610 | GAGCAGCTTGTGTTT[G/T]TTCTTCCTTGTCTAC | 57630 |
| rs573141641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147425 | TAATAAATCAGTGAA[A/C]AAGTATTTCCCCTAC | 57630 |
| rs573155215 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241826 | GGCCCTCAGATGCTC[A/G]GTAAAGTCAACCTTG | 57630 |
| rs573182612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133790 | AAAAAAAAAGAAAAG[A/G]AAAGGAAAGGAAATT | 57630 |
| rs573219683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191101 | GCCATCTATGACAAA[C/T]CCACAGCCAACATAA | 57630 |
| rs573245147 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266695 | GACTTGAACTCCTGG[G/T]CTCAAGTGATCCTCC | 57630 |
| rs573271426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234197 | ATGTCAATTTTTTTT[C/T]AAATTGTCCCACTTG | 57630 |
| rs573302338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198126 | CAATATTTGTGAGTT[G/T]GAGAAAAAGGCAAAT | 57630 |
| rs573321340 | in-del | -/T | 0.0337553 | 0.125452 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146137 | TCTATATATTATATA[-/T]TCTATATATTCTATA | 57630 |
| rs573325228 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272721 | AGGTTAACTTTCCCC[G/T]GGTCACACAGTAAGT | 57630 |
| rs573329636 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135954 | GTTTGGACCATGGCA[C/T]CTTAAATCTGGGTGG | 57630 |
| rs573335900 | snp | A/G | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093906 | TGCTGAGACTTACGG[A/G]TTATCATACTATTGG | 57630 |
| rs573344897 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268011 | ATCAGGAATCCATCA[A/C]CTGCAACATAATTTA | 57630 |
| rs573349564 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265890 | AGCAGAAACTATTAG[A/G]TCTAAATTCTATAGG | 57630 |
| rs573354579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263938 | GTGGGTAGTTGAGGG[A/C]GTAGGGAGGGGCTGA | 57630 |
| rs573366309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219956 | TTAGCAATCAACTTC[C/T]AGGCGATCAGTACAA | 57630 |
| rs573367927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197593 | TGCGCCACTGTACTC[C/T]AGCCTGGGCGACAAA | 57630 |
| rs573377930 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178263 | TAAACAAATAAACAA[A/C]AAAAAAAAATTTTTT | 57630 |
| rs573390372 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177412 | ATTAAATAAGAAGAC[A/T]AATAAGCAAAGGCCA | 57630 |
| rs573427407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226136 | AATGTTGTGACTCAT[A/G]GTTTGTCTCTTTTGT | 57630 |
| rs573433335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104243 | ATACCACAAATGAGA[A/G]GGAACACAGGAGAGA | 57630 |
| rs573459633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184331 | CAGAGCACATCACAC[A/G]TGCACACATCCAAAT | 57630 |
| rs573486786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221191 | AGGCTGAACACAAAA[C/T]CGCAGGCAAGTCAAG | 57630 |
| rs573488404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228623 | TCATCTCCTCTCCAG[G/T]TCAGCTGATTAGCAA | 57630 |
| rs573504443 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242297 | CCACAAAAATACCAC[C/T]TATGCAGCGACCCAT | 57630 |
| rs573521325 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118457 | TGTGGTATATTATTA[G/T]TAGTAGTAGTAGTAT | 57630 |
| rs573526489 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206185 | ATTAGGAAAATATGA[C/T]AAAACCTATGGAATC | 57630 |
| rs573550263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228025 | AAAAGCAACATAACG[C/T]ATTTTTAACTACTAT | 57630 |
| rs573550386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097120 | AGTCCTCTCTGAACC[A/G]CCTGCCCACAGGCTA | 57630 |
| rs573560644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209382 | AGGATCCACTTCATC[C/T]GGGATGCTTTCCCTG | 57630 |
| rs573565032 | snp | A/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271333 | GCTCGGGGACGGACG[A/C]CTTCTCCCTGAGGAG | 57630 |
| rs573598057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175218 | TTCTACTGCTACCAG[C/T]CCAAGCCAGATCAAC | 57630 |
| rs573617166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097621 | TCTATTTTTCCAGCA[C/T]TATTTGCATTACTCC | 57630 |
| rs573627065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154349 | TGAAAACGTTGGCAA[A/T]CTCACTCTCTATGGA | 57630 |
| rs573648910 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212534 | CTTCCATTTTTTTCC[C/G]TTTTAAAAAGACTCT | 57630 |
| rs573658940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183180 | TGGAAGGCACCTGTA[A/G]TCTCAACTACTAGGG | 57630 |
| rs573662877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154930 | AAAAAGACTTTACTA[G/T]GTCAAGCTTGGCCAC | 57630 |
| rs573681477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233873 | GTCTTCCTTCCCCCA[C/T]GATTTCTCTATTTCC | 57630 |
| rs573684131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174770 | ACCCCAAACCAATTA[A/C]ATAAAAATCTCTGGG | 57630 |
| rs573707095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270799 | ACCACCGCCTTCTCC[A/G]CGGCTAGGGGTCCGC | 57630 |
| rs573721518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167176 | AAAAACAAGCAAAAG[A/G]TGTGAATACACATCT | 57630 |
| rs573769782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270115 | CTGCGCCGCTCTCCC[C/G]CCACCGCCAAAATAA | 57630 |
| rs573777050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204916 | TTGAAAAAAAAAATT[C/G]TAATATTAAGAAGCT | 57630 |
| rs573793063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256123 | TCTAGTTTCCCTTAC[A/G]GAAAGTCTTAGGAGT | 57630 |
| rs573807339 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158387 | AGTCACATGTGCAGC[A/G]GGACTGGGGAGCATA | 57630 |
| rs573809927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242016 | TCTGAAAAGATTATA[C/T]ATATGAACAATGAAG | 57630 |
| rs573838149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126148 | TAATGAGATTGTGAA[G/T]TCAGGGACTGTCTCA | 57630 |
| rs573859082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265302 | ATTAAATAAAGCAAC[A/G]AATAAACTAAGTATA | 57630 |
| rs573877265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162841 | AAGAATGTGGGCTGA[C/G]CAAGGCCAGCCTTTG | 57630 |
| rs573880970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255324 | AGGCTCTTCACTGTT[A/G]CAGCATTTGCAAAAT | 57630 |
| rs573881006 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121394 | ATATGGTATGAAATC[C/G]CACTGGGAAGCACAA | 57630 |
| rs573904973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197649 | AAAAAAGCCCACCTT[A/G]GAATAATTGTGTTTG | 57630 |
| rs573917927 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138378 | CATCTCCTCCATCCC[A/T]AACACAACATCCTCA | 57630 |
| rs573933131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141551 | GAGATTAAGCATCTA[G/T]TTTCTTTTTTTAGGA | 57630 |
| rs573940258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235643 | ATGCCATATTAATCA[C/T]TACATCAGCAATGAG | 57630 |
| rs573945964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176062 | CCATGGAGCACACAG[A/T]AAGAAGGTGGCAAGC | 57630 |
| rs573957260 | in-del | -/T | 0.00159617 | 0.0282053 | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093973 | CTAGCACTCACCAGA[-/T]TATTTTAGTAACTGG | 57630 |
| rs573967877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228304 | CATGGCTTAAGATAA[C/T]ACAAATTTGTTATCT | 57630 |
| rs573983267 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272870 | GCAGTGTGTCTCTTC[C/T]CAAGGGAAAGAAGAA | 57630 |
| rs573993380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142016 | GTATAGACAGGGTTT[C/T]ACCGTGTTAGCCAGG | 57630 |
| rs573995283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133842 | TAAGGAAAAGGAAGA[C/T]AGCAATCAGGTCAAT | 57630 |
| rs574029912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234850 | TTGTTTGTTGGGGAG[C/T]GTGGCTGTCCTGTGC | 57630 |
| rs574031057 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224232 | ATAAATATGATTTTG[C/T]TCTAAGTGTAAGGAA | 57630 |
| rs574048774 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185180 | TAGGTCCCTACCACA[G/T]GCCAAGCACTGTGCT | 57630 |
| rs574055215 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138185 | TGGTCTAGCTATCCC[A/C]CCTTGAGAATAAAAA | 57630 |
| rs574098873 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202608 | CCTCTGAAAACACAA[C/G]GGTAGTAAATACCTA | 57630 |
| rs574109684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192192 | ATGAACTCAAACAAA[A/T]CAACAAGAAAAAAAC | 57630 |
| rs574122326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148128 | AATTTGTTATGAAAC[A/G]TTAAAATGCCCTATA | 57630 |
| rs574128970 | in-del | -/TAAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208526 | TGATATAATAATAAA[-/TAAT]TGTTTTCATTCCTAA | 57630 |
| rs574144870 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097680 | GGTGGTGTATGGTAG[A/C]CAACCTCCAAGATGG | 57630 |
| rs574147788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246429 | ATGTGCAACCCCGCT[C/T]ATCTGTATTCTGTCA | 57630 |
| rs574152663 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111971 | TACTGTTCAAAGGAG[G/T]AGCCGGTTAGAAGAG | 57630 |
| rs574172244 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191491 | AATCTACAAATTCAA[C/T]GCAATCCCCATCAAA | 57630 |
| rs574195848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169397 | AGGTCAGGAGTTCAA[A/G]ACCAGCCTGGCCAAC | 57630 |
| rs574209115 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245480 | TCTACTATATTTTGA[A/T]AGCACACAGATGACA | 57630 |
| rs574248983 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162949 | CCACACCCTCCATCC[A/T]CTCCTTACCCAGCTC | 57630 |
| rs574254337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176796 | TCCACCCGCCTCAGC[C/G]TCCCAAAGTGCTGGG | 57630 |
| rs574259132 | snp | A/C | 3.54679e-05 | 0.00421102 | missense | SH3RF1 | GRCh38.p7 | 4:169269197 | CCAAAAGATCCAACA[A/C]GGCTGATTCATCCAT | 57630 |
| rs574279039 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228717 | GAGGGAAAGGGAATG[A/T]CACATTAGTCTGCCT | 57630 |
| rs574310505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130452 | TGCCTCATTTGGTAC[A/G]CCACCATGAATCAAA | 57630 |
| rs574312968 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230877 | AAAAAAAAAAAAAAA[C/T]TACTGAGTCCCCCTC | 57630 |
| rs574318678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180023 | ATGCTAAAGAAACCT[A/G]CATAAACTTTGGCCA | 57630 |
| rs574343577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188076 | TAGGAAGAAAGAAGA[A/G]GGGATTCTTCCTAGA | 57630 |
| rs574363152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238507 | CTTGTCCTGATAGAT[A/G]CCTGTGAGGTAGGCA | 57630 |
| rs574379716 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187520 | ACAACGAATTTCTGT[C/G]TGTGTGTGTGTGTGT | 57630 |
| rs574402820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237879 | TATGATTTCCCCCCC[A/G]CTCCACACCCTTGAA | 57630 |
| rs574428361 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265727 | ATCCACCCACCTCCT[C/T]GGCCTCCCAAACTGC | 57630 |
| rs574443747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196081 | TGGCCTCCCAAAGTG[C/T]TGAGATTACAGGAGT | 57630 |
| rs574458282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123483 | GTGCAGAAACAAATG[A/T]GGTGCAGAGCCACTT | 57630 |
| rs574470589 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251398 | TCAGATAATCTCAGT[C/G]AAGCAGCCTTAAAAT | 57630 |
| rs574509841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194539 | TTATCCATATGATTA[C/T]GTGTGTCAGTTTATT | 57630 |
| rs574544205 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217121 | TGAGCCAAGACCATG[C/T]TATTGCACTCCAGCT | 57630 |
| rs574563864 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148370 | GGTTAGCTACTAGAG[C/T]GTTTATTAGACAGTC | 57630 |
| rs574571655 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097437 | TTGGCTCAGAATTTG[G/T]AGTTAGTGGGAAAGG | 57630 |
| rs574572585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194107 | TTAGAAAACAGAGAC[A/G]GAGACACATACTCAG | 57630 |
| rs574609046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166143 | ACACATGAAGAAAAT[A/T]AAAATGTAAACCACA | 57630 |
| rs574682092 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180437 | ACACACTGCCACAAC[C/T]GGAGGAATTTTAACT | 57630 |
| rs574683947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219291 | AATTTATGCCAAATC[A/G]TTTCTGTTCAATCAA | 57630 |
| rs574693930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203291 | CACGGTGGCTTATGC[C/T]TGTAATCCCAGCACT | 57630 |
| rs574697414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225239 | TTTGAAAAGGAAGGT[A/G]GTATGACCTGCTTCG | 57630 |
| rs574697440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217782 | TGGCTAGTGATGGTC[A/G]CTCAACAATGTGAAT | 57630 |
| rs574714138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153104 | TTACCTAAGTCGGCC[A/G]GCAGGAGTCGAGGGG | 57630 |
| rs574730851 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184380 | TTGAAGATTCTAGAA[A/G]GCCAGATGGCAGGGC | 57630 |
| rs574791935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202931 | TGTATATATCTAAAG[A/G]AAGAAGACATAGCAT | 57630 |
| rs574807600 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096265 | ATCTTAAAAAAAAAA[A/G]AAAGTTTCTCTGTGT | 57630 |
| rs574824571 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249120 | GTAGTCCCAGCTACT[C/T]AGGAGGCTCAGGCAG | 57630 |
| rs574855803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131710 | CTTTTCTGAACCGCA[A/G]GTGGGAAACTGAAAG | 57630 |
| rs574859361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145761 | TAAAAACTATATAAA[A/T]TATATAAAATATTAT | 57630 |
| rs574874117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209912 | CTCTCTCCCTAGTCA[C/T]CCAAGTAGCTGGGAC | 57630 |
| rs574880902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261237 | CTGACCTCCAAACCA[A/C]ACTCTTCCCCATACA | 57630 |
| rs574919038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159124 | CCTTGACCTAATCTT[A/G]TAAGCAATTCTGCTG | 57630 |
| rs574924361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146326 | CCTCTGCCTCCTGGG[G/T]TCAAGCAATTCTCCT | 57630 |
| rs574943697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182416 | ATTAAGAATGCCAAT[A/G]TATTTTTTCTTTTCA | 57630 |
| rs574947705 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113916 | AGGGCACCATGTAGA[A/G]AGGAGATCTGCATTT | 57630 |
| rs575025013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159776 | GCTGGATGCTTTCCC[C/T]TTTAGATGAATTCAC | 57630 |
| rs575042360 | snp | C/T | 0.000299825 | 0.0122402 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116506 | GCCTGGCATCAGAGG[C/T]GCAGGTTGTGGGGAG | 57630 |
| rs575054897 | in-del | -/GGACA | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178530 | GGCCCAGACCTGGGT[-/GGACA]GGGCTCTGGAACACA | 57630 |
| rs575083231 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261936 | GAGTATTTTTCTTAC[A/T]CTGAGTATTTTTTAA | 57630 |
| rs575103223 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172713 | TGGCAGGGGTGAGGG[G/T]GTTGCCAGAGGAGAC | 57630 |
| rs575123836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224880 | GAGGCTGGAATGGAA[A/C]ATTGGGGCCAGATTC | 57630 |
| rs575137447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240625 | TCTATTTGCAGTGTA[C/T]AGCATTTTTAATATG | 57630 |
| rs575145396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269939 | AAGCGCCCTTCAGGG[C/G]AGTAGTTGATAAACT | 57630 |
| rs575168051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109189 | TAAGAAAGCACACAC[C/T]AGTCCACGGACCCCC | 57630 |
| rs575183801 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269266 | TCATAGTTGTGTGCA[C/T]CCCTTAAAATGACTC | 57630 |
| rs575187844 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097250 | TGACATGGGCGAGGC[A/G]GCAATTCTGAGGAAG | 57630 |
| rs575202345 | snp | A/G | | | missense | SH3RF1 | GRCh38.p7 | 4:169156519 | ATCTGCACAAAGTTG[A/G]TGGGGAAAAAGCCAT | 57630 |
| rs575205580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231666 | TTTTTGCTCAAAGCT[A/G]CTATAGAATACTCAC | 57630 |
| rs575220294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124406 | AATCACTTCTTGTCA[C/T]AAAATACACTAAGTT | 57630 |
| rs575246426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195585 | AATCTCGTACCATAT[C/T]CTTTAGGTCTCTTAA | 57630 |
| rs575268830 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124962 | TCCAGGCCAGCCCAG[A/G]CACCAGAGGCCAAGT | 57630 |
| rs575296436 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124480 | CATTAAGATATGGCA[G/T]CAAAGAGGATATTCT | 57630 |
| rs575326377 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166952 | CCAGATATCAAGAAG[G/T]TGATATCTTCGACAC | 57630 |
| rs575344235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189014 | AAGAAAAAAAGAAAA[C/T]GAAAACTTCCAGGGA | 57630 |
| rs575367182 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145030 | ATGAAAAAGGCAAAG[A/C]GTTTCAGAGAGATTA | 57630 |
| rs575382933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145552 | AGCACATGTACCCCC[C/T]GAATCTGTAAAAATA | 57630 |
| rs575411804 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218569 | TTTACCCTTTCCCTG[C/G]AGCCAGGAGAGCCTG | 57630 |
| rs575425768 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216139 | ATCTGTGATATATGT[C/T]AGCTATATTTGTATC | 57630 |
| rs575440648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166215 | AGAATTAAAATGACT[C/T]CTACTAACCAACAAT | 57630 |
| rs575473542 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246774 | TTAACTGGGTCTGAT[C/T]CACTAATGTAAGTCA | 57630 |
| rs575476181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153196 | TCTGGTACCCTCTGC[A/G]TGATAGTCTAATCTG | 57630 |
| rs575491510 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243340 | CAACATGGAGAAACC[-/T]CGTCTCTACTAAAAA | 57630 |
| rs575500956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173752 | ACCATTTACAAGCTA[C/T]CTTTTTTTTTAATAA | 57630 |
| rs575510769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197481 | AAACACAAAAATTAG[C/T]CAGTCGTGGTGGTGC | 57630 |
| rs575518958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210957 | GCTTGTCTAAGGTTT[C/T]ACTTTTAACACATGC | 57630 |
| rs575528489 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200921 | TAGAATACTTGGCCC[C/T]TTCAAAGTAAAATGA | 57630 |
| rs575560684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140003 | CATATTTTTTCTGCA[C/T]TTGATTTTTATGCAT | 57630 |
| rs575579863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218818 | GATTCATTAATGGAA[A/G]GAAGCATTTAAGAAT | 57630 |
| rs575603477 | in-del | -/CT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239240 | TTATAAATCTACCTA[-/CT]TTGTAAAAGGGGAAT | 57630 |
| rs575614117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196809 | TCATTTTAATAAGCT[G/T]TTCCTTTACTATATC | 57630 |
| rs575621158 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236185 | ACACATGGCAGGACT[G/T]CCCTTTCCGACCTCC | 57630 |
| rs575649945 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134901 | CATGTTCTAGTTGTG[C/T]GTTGTGCGTGTCTTT | 57630 |
| rs575676775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203366 | GACCAGCCTGGGCAA[C/T]ATGGTGAAACCCCAC | 57630 |
| rs575717399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254657 | AGCATGAACCAGCAA[A/C]GTAGTGAGTTATTTT | 57630 |
| rs575761412 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156229 | TAAGAAGTCTGTGCA[C/T]AAAATTACCTTCCTT | 57630 |
| rs575764890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175294 | AGTCTTGCCTGTTAA[A/C]CTCAGAACGGCTTTC | 57630 |
| rs575767036 | snp | A/G | 0.0209421 | 0.100162 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169270919 | GCGGCGGCTGATGCA[A/G]ATGCGGCCCCACCGC | 57630 |
| rs575772313 | snp | C/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271819 | GGGGCTCTGTTATCC[C/T]TGCCCTAAGTGGGGA | 57630 |
| rs575787399 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227091 | GGATTGCTTGAGCCC[A/G]GGAGGTTGAGGCTTC | 57630 |
| rs575849493 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265469 | TAAGAGATATTAAGA[G/T]AACTTAAAAGAATTT | 57630 |
| rs575887504 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229492 | AAAAAAAAACCTATT[C/T]GGTGGCCACATACAT | 57630 |
| rs575917271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143027 | TTACTCAAGAGTCTT[C/T]TAAAATTGATATGAA | 57630 |
| rs575920008 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096318 | ACACCTTATACATCC[A/G]AATCCAGACTAACAA | 57630 |
| rs575925108 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168849 | TGTCCTTTGTTTCTT[-/A]GGGGTGGAATCTCAA | 57630 |
| rs575952677 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200603 | TTCATAACTTACATA[G/T]ACCTTACATAATCTT | 57630 |
| rs575962411 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228075 | TCCCTATTCTACTTT[C/T]TCAGCTGTTTCCAGG | 57630 |
| rs575974257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102844 | ATCCTTTCTTACTAT[C/G]AGATTGCTTAAGTCT | 57630 |
| rs575993065 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250931 | GCTGACCTTCCTTCC[A/G]GGCAGGGCAAAGACT | 57630 |
| rs575993623 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181349 | TTCACTGCAACCTCC[A/G]CCTTCCAGGTTCAAG | 57630 |
| rs576020979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143483 | CATAGCTCCTGTAGG[C/G]AAAGAAGCTGCAACA | 57630 |
| rs576023775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241147 | AGACAGGAGAATGGC[A/G]TGAACCCAGGAGGCG | 57630 |
| rs576036001 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103590 | TGAACACAAGTAATC[C/T]CTAAATTCTATACTT | 57630 |
| rs576040176 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233235 | GCCTGGGCAACAGAG[A/C]AAGACTCCATCTCAA | 57630 |
| rs576056240 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178983 | ACATTGCATAGTAGA[A/C]CCTACCCATGTGTGC | 57630 |
| rs576057190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257678 | GTTCTAAAGTGCAGG[A/G]CATTTTAATATGCAG | 57630 |
| rs576087175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243471 | TGAGCCAAGATCGTG[C/T]CACTGCACTCCAGCC | 57630 |
| rs576114411 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190768 | GGAAAGGATATAACC[-/A]AAAAAGAAAACTACA | 57630 |
| rs576123357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108592 | ACCTGGGCTATAGAT[A/G]AGCAGAGCCAGCTGA | 57630 |
| rs576133803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206253 | AAATGATATCTTAGC[A/G]TGCCACACATGATTC | 57630 |
| rs576148897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230214 | AAAAATAAAAATAAA[A/T]TAAAAAACAATGTTT | 57630 |
| rs576199151 | snp | G/T | 0.000927895 | 0.0215194 | missense | SH3RF1 | GRCh38.p7 | 4:169136403 | CTGATGAGGACAGGG[G/T]GGCTGATCTCCATGG | 57630 |
| rs576209548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246513 | CACTACGTGCCTAAA[A/G]GAGAAAGTAGAAAAA | 57630 |
| rs576266977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149739 | AAAGGAAAATAATAC[A/T]TCTAAAGGAAAAAAT | 57630 |
| rs576270360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245722 | AAAATCCGTATGGCG[A/G]TGGTAGGTCAGTAAT | 57630 |
| rs576289311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099336 | TCAAGCAATCTTCCA[G/T]CCTCAGCCCCAGAAA | 57630 |
| rs576311623 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105297 | TAAGATATAAAAAGA[C/G]TCCACTATTTTGAGT | 57630 |
| rs576313269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113708 | CATGAAGATTCATGA[C/T]TAAGTGACAACAATC | 57630 |
| rs576330426 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170033 | GAACAATTTTATCAA[C/T]AGATAGATTAATGGG | 57630 |
| rs576366800 | snp | C/T | 1.74024e-05 | 0.00294972 | missense | SH3RF1 | GRCh38.p7 | 4:169116288 | CTATCCTTGTCTGGT[C/T]TGGTTGCTGAACTGT | 57630 |
| rs576376402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208843 | AGTAGGAGTGGGCCT[A/G]CGCAGAAACCCCTGG | 57630 |
| rs576378798 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238006 | AAGAATCCCCCTACA[C/T]TTGATGTCTCCTCTT | 57630 |
| rs576403069 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151221 | GTTTGAATTCTAATG[A/G]GGAAATGGAGGGTGA | 57630 |
| rs576422435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244289 | CATTTTTAAATTTTT[C/T]CATGTGAATTGAGGA | 57630 |
| rs576422509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236382 | TAATGACTATAATGA[A/G]CGGTGTCCCTCTGCC | 57630 |
| rs576423224 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104037 | CTTCTTTTCAGATGA[A/C]CTGAACAGCAGGAGC | 57630 |
| rs576468158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144403 | GCAAAGACTTCTGTG[C/T]TGGGAATAGGGTCCT | 57630 |
| rs576486365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158206 | CATAGGTCTCTCGTG[C/T]TTGGTGAGTAGGAAA | 57630 |
| rs576488680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223577 | CACCACGACACACCA[C/T]GAATAAGACAGACAG | 57630 |
| rs576489340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179765 | CTACATTTGCTTCCA[A/G]GTGAAACAAAATTTA | 57630 |
| rs576509844 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230938 | TTTAAGTTTATAGCC[A/C]TCAAGTATAAACAAT | 57630 |
| rs576530720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267215 | GCCTCTCCTTAAATT[C/T]CTCTTTATCAGTGAA | 57630 |
| rs576561737 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184540 | TTGAGCCAAATTTAA[C/T]AATGTAATAGTATTC | 57630 |
| rs576566583 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250000 | ATTTGAATCCACACT[A/G]TATCAAATGAGGAAA | 57630 |
| rs576602643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180418 | ATAATAACACTGTAG[A/C]TTAACACACTGCCAC | 57630 |
| rs576606815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157288 | AGCAGTGAGTGAACA[A/G]TCACAGTACCTGCCA | 57630 |
| rs576609700 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132159 | CATGGACACCCTCCA[C/T]TGGTAACAGACATTA | 57630 |
| rs576611356 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105290 | ATTTATATAAGATAT[-/AA]AAAGAGTCCACTATT | 57630 |
| rs576616753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253177 | AGCTCTTCATTCATA[A/G]CATACCTAGAAACCA | 57630 |
| rs576621513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266305 | CAACATTCCACGTTA[A/T]CACTTTCAGCTTTGC | 57630 |
| rs576630204 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137013 | CCCTGTTGCACAATA[A/G]TGGTTGGGTATTTGC | 57630 |
| rs576647729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114638 | GAGACACATTGTCAT[C/T]AAGCCTTAAAATCTA | 57630 |
| rs576672159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129618 | GAAATTAAATAATGA[A/G]TCTTTAATGTAGAGA | 57630 |
| rs576719522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115567 | TGCAAGAAAACAAAC[C/T]CAGGGCTCCCACTAA | 57630 |
| rs576735314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130277 | CTTTCTGTTATTTGG[A/G]GAAGGTAGAATCCCT | 57630 |
| rs576768522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245441 | CAATTATCCATCTAA[A/G]TTTATCTATATAGTC | 57630 |
| rs576769431 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252662 | CTATTTTTTTGGCTT[A/T]ATATCCCAGTATGTC | 57630 |
| rs576779676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202243 | AGTGTTAGTGCTTTG[A/G]CCCTAACATAAACTG | 57630 |
| rs576785846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193405 | TTAGCTTCCAACAGA[A/C]AATGCACAAGGACTC | 57630 |
| rs576803254 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137194 | AAAAGCTGGCAGAAA[A/C]TCTTAATATGTTTTT | 57630 |
| rs576841579 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249713 | GGATACATTTCCAGC[A/G]AGCTGTGACTCTTTA | 57630 |
| rs576845380 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209854 | GAGTGCAATGACACA[A/G]TCACGGCTCACTGCA | 57630 |
| rs576889745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251759 | AAAGGTGGCTTCCTT[A/C]GTAAGGAAACCCAAT | 57630 |
| rs576909317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217873 | AAAACAAAAAAAAGT[C/T]TAATGAGGGAAAAAA | 57630 |
| rs576921689 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167083 | CTGTGTTTGCCCTGA[A/C]AAATAAAATTTAACC | 57630 |
| rs576926547 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222422 | GTGAACTGAGATTGC[A/G]CCACTACACTCCAGC | 57630 |
| rs576960063 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095560 | CACGAGTGCATCACT[G/T]ACCACCACTATCTCA | 57630 |
| rs576973503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224267 | CCAGTAGAGAGCTAT[A/G]AACAGAGGAAATGGC | 57630 |
| rs577001187 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130406 | TCTTACCTACAGAAT[A/T]CAACTGCCATTGGCT | 57630 |
| rs577065556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187457 | TCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 57630 |
| rs577117389 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231552 | GTCTGGGTGACACAG[C/T]GAGACTCCGTCTCAA | 57630 |
| rs577117903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210576 | CAAAATATTTTCTTT[C/T]CATAATAACATGTTA | 57630 |
| rs577186886 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187377 | TTTTAACTTTTTGTG[G/T]AGATGGGGTCTCTAT | 57630 |
| rs577191566 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193451 | ATTTGGGGGATATTT[A/G]TTCTTTTAAACATAA | 57630 |
| rs577215015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165582 | TAGTCCAATATTGTG[C/T]CACTGCACTCCAGCC | 57630 |
| rs577227355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213172 | GAATGAGAATTCCTG[G/T]TGATCCACATTCTCA | 57630 |
| rs577247776 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184931 | CTGATTCCAACTCTA[A/G]GTCCCTCACCTTAGT | 57630 |
| rs577248472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217710 | GAATAGGGAGTTACT[A/G]TTTAATGGATACAGA | 57630 |
| rs577276705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268140 | AAATAATTAGCTTCA[C/T]CTAAAATTATTTCAG | 57630 |
| rs577278224 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164824 | ATAAACTCATTTGGT[A/G]GTTAGGAGGAAACAG | 57630 |
| rs577281383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097707 | ATGGCCCTAGTGATC[C/T]TTGCTTCCTGGTATT | 57630 |
| rs577287962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152079 | ACTGTATTCAGTCCT[C/T]AAAAAATATACCCTT | 57630 |
| rs577292505 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129523 | TTCAGAAGGGAAATC[-/A]AACATAATCTAAGGG | 57630 |
| rs577293883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261130 | CATGGAGCTTAGGTC[C/G]CTATGGCTCCGCATC | 57630 |
| rs577305562 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203081 | CTGTTTATTGTTAAG[A/C]AAATGCTAAACAAGC | 57630 |
| rs577308907 | snp | C/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216925 | GGAGGCCGAGGCAGG[C/T]GGATCACTTGAGCTC | 57630 |
| rs577335097 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220657 | CTCCAATGGGATTAG[-/C]TTTCACTGTACTGGA | 57630 |
| rs577381369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115770 | CAGGTGCCCAGAAGG[C/T]TGGGGACCACTGTTG | 57630 |
| rs577396170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195699 | CTTTTCTTTAGTTGT[A/G]TCTGATTTGTTATAA | 57630 |
| rs577423740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247337 | AAATATTTACTGAGA[A/G]AGTGAATGGTGGACG | 57630 |
| rs577480639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159044 | AATGACACCCTCCTG[C/T]GACCTCTGACTTTCA | 57630 |
| rs577516269 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173642 | AGGGTTACACATGTT[-/A]GCTCTGGAGAAAACA | 57630 |
| rs577560995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214049 | TCAATATACACTGAT[A/G]TAGTTTGGATGTCTG | 57630 |
| rs577568870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128844 | TCCCTATTCCTGGTA[C/T]AGACAGCAAAGAAAA | 57630 |
| rs577599535 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227745 | CATTATCTACAACCA[A/T]AGAACAGTGCCCATC | 57630 |
| rs577622085 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229658 | GGCAAGAAAGTGAGA[A/C/G]GTGAATACTAATGTA | 57630 |
| rs577631934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253955 | GGAAAACATGATTTC[C/T]AGACCACCATGGTGG | 57630 |
| rs577632388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221122 | ATTTGCTGACACAAC[A/G]TCATTCTGTGCTCTC | 57630 |
| rs577675248 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271455 | GCCTCCTCCTCCCCC[C/T]GGCGGGGCTGGGAGC | 57630 |
| rs577686083 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236312 | ACTTGCCAATTCCCT[A/T]CCTGGAAGCATGTGC | 57630 |
| rs577698282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220475 | CCTTTTTCTAGTACA[C/T]TTAGAGTGCATATTT | 57630 |
| rs577700984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122000 | TTGGTGAGCCATAAC[A/G]CTGTCATCAGCTCAT | 57630 |
| rs577749864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235776 | GGCTCACTGCAACCT[C/T]CGCCTCCCCAGTTCA | 57630 |
| rs577758450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242739 | TTGTTATAAAAGCGC[A/G]TTTGGCCCCCATTGC | 57630 |
| rs577760108 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261603 | AGAAGTGAGACCATC[G/T]CAAAAAAAAAAAAAA | 57630 |
| rs577760844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263728 | GCCTTAGGTACTACT[A/G]AGTCCTGGAAAGCAC | 57630 |
| rs577774713 | in-del | -/CCT | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195303 | CTGGTTATAATTATA[-/CCT]CCTAGGAAAATTTGT | 57630 |
| rs577791771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118606 | GAGTACAGGCACGCG[C/T]CACCATGCCCGGCTA | 57630 |
| rs577801663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258756 | AATCTAGTTTTATTA[C/T]ATAATGTTTATTCTA | 57630 |
| rs577821387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250110 | GTCACTTCTCTTCCT[A/C]AGAATATGTTAAGCA | 57630 |
| rs577847715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119531 | TATTTTTTTGTTCTT[C/T]GTTGCATTTCTCTTA | 57630 |
| rs577872224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126353 | AAAGTTCTGACCATA[G/T]CCTACTCTTCACCCT | 57630 |
| rs577883154 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108158 | AATTGTTTTACCAAG[A/G]TGTCAACTACATCAT | 57630 |
| rs577887976 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204334 | TCATTCAATCATCCT[A/G]TTCTCTGTCAAAGGT | 57630 |
| rs577889863 | in-del | -/T | 0.461148 | 0.133852 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228388 | GTTGGCAGCGCTGTG[-/T]TTTTTTTTCTGGAGG | 57630 |
| rs577893296 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249480 | GAACTGTGAGAAATA[A/T]ATTTGGGGTATATTT | 57630 |
| rs577894257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163019 | CAGCTCTTGACCAAA[C/T]AGCAATCAGTCAATT | 57630 |
| rs577933537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127010 | TTGGCTGGTCCAGAG[G/T]ATCGGGGATTATTCA | 57630 |
| rs577945380 | in-del | -/ATA | 0.00279162 | 0.0372561 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146057 | TCTATATAAAATATT[-/ATA]TATTCTATATAAAAT | 57630 |
| rs577996761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115361 | CTGTATTTACAGCCG[C/T]TCCCCATCACTTGCA | 57630 |
| rs578016090 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113861 | TTCAAGGGTATAGCA[C/T]TAGAGAAAAGACACA | 57630 |
| rs578030864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180909 | CTTGAGCACCTATTA[A/G]CATTCTCAGCACTAG | 57630 |
| rs578044660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192668 | AAGAAGTCATTATAT[G/T]AAAAAGATACTTGAA | 57630 |
| rs578085364 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142070 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 57630 |
| rs578131433 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134634 | CCTTCAGAACCTTAC[G/T]CAAAAATCTTTAGTT | 57630 |
| rs578144432 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185251 | CTCTGCAATCTGGGA[A/T]CCCACACCTGAATGC | 57630 |
| rs578173504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223491 | GCATGAGGCAGGCAG[A/G]GAAGAGACATCCGCT | 57630 |
| rs578190469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135110 | GAGGCCCAGGTAGGA[A/T]GTTCACTTGAGGCCA | 57630 |
| rs578195576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170329 | AGCAAGAGCCCATGC[A/G]TGCACCTGAGACTAC | 57630 |
| rs578218864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222956 | CCTGTCCTCGCATGG[A/G]TTTTTATGAGGCACC | 57630 |
| rs578228144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207165 | GTTTTGCTAGGTTGC[A/G]CAGGCTGGTCTCAAA | 57630 |
| rs745325889 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230160 | AGTGAGCCAAGATCA[C/T]GCTGCTCCAGCCTGG | 57630 |
| rs745348454 | in-del | -/AAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230857 | TGAGAAACCACCTCA[-/AAA]AAAAAAAAAAAAAAA | 57630 |
| rs745354220 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104422 | AGGTTGACTCTTAGA[A/G]TAAGAGATTCAGTGA | 57630 |
| rs745355440 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138643 | CTATCAAATCTAGTT[G/T]ATATCATGTTTAGAT | 57630 |
| rs745372377 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107722 | CAGCACTCTATTCCA[C/T]AGGCATGGACGTGAG | 57630 |
| rs745386005 | in-del | -/TTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214858 | AAACTTTCAGGAGTT[-/TTG]TTGTCAATTCTTTTG | 57630 |
| rs745426333 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202967 | ATCTAGATAGCAATG[C/T]ATATCCTCCTGAACA | 57630 |
| rs745427204 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231427 | AAAAATTAGCCAGAC[A/G]TCATGGCGCATGGCT | 57630 |
| rs745429128 | snp | A/G | 1.69453e-05 | 0.00291073 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122269 | GAGGATTCAAAGTCT[A/G]GTATAGGAAAAACAT | 57630 |
| rs745435906 | snp | G/T | 1.67223e-05 | 0.00289151 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268886 | GCTCTGCAGATCTTT[G/T]GAGCTACAATTAGCC | 57630 |
| rs745456286 | in-del | -/A | 1.69292e-05 | 0.00290935 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155442 | TTATTTAGTAAGCTG[-/A]ATATTAACACAGTTC | 57630 |
| rs745457211 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139841 | GCCATCTTACCTCTA[C/T]TGTTCACAGCTTCCT | 57630 |
| rs745460069 | in-del | -/CTTA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152278 | CAAAGCAAGAGAACC[-/CTTA]CTTACCCTTATCTTA | 57630 |
| rs745487413 | snp | A/G | 1.88795e-05 | 0.00307236 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268773 | ATAAAGAAAAAATGT[A/G]GACATTACCACCTTT | 57630 |
| rs745490819 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245018 | TCGTATTCTGTAAGC[A/G]GATATTCCATCTTAA | 57630 |
| rs745530797 | snp | A/G | 0.000167929 | 0.00916167 | missense | SH3RF1 | GRCh38.p7 | 4:169107078 | AGTTCGGGCCCCACC[A/G]CTCCCTGGAGAGGAA | 57630 |
| rs745534235 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248725 | CAGTTTCCCAATCTG[C/G]AACTTGGAGCTGTTC | 57630 |
| rs745543662 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193422 | TGCACAAGGACTCCA[-/C]CCCCCAGAGAGTTAT | 57630 |
| rs745569379 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171782 | CACAGAAGACTCCTA[C/G]AGAAATGAAATGTGA | 57630 |
| rs745593665 | snp | C/T | 1.65312e-05 | 0.00287495 | missense | SH3RF1 | GRCh38.p7 | 4:169120832 | ACCTTGTGACTGGTG[C/T]CACATAATTGCCAGG | 57630 |
| rs745596499 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158728 | TAGCATTACTTATAT[A/C]ATTGTCTGCCCCCCG | 57630 |
| rs745620912 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223679 | GAGCTTACTTTCTAA[C/T]GGGGTGATGGGCAAG | 57630 |
| rs745621349 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222705 | AGTTTATTGCTTCCC[C/T]TGTTAATCTTTCACC | 57630 |
| rs745670127 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130799 | TACTAGAAAGAAATT[C/G]AGTTATTCAGGTCAT | 57630 |
| rs745707077 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209947 | GGCACGCATCACCAC[A/G]CCCAGTTAATTTTTG | 57630 |
| rs745720349 | snp | A/G | 0.000120477 | 0.0077604 | missense | SH3RF1 | GRCh38.p7 | 4:169117780 | GAAGCATTTGTCACC[A/G]CCCTGCCAAGACACA | 57630 |
| rs745739788 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108115 | GTGAATGTTCTTTCT[-/G]ATGACCAAGCTTAAC | 57630 |
| rs745765925 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119092 | TATTCCTCTAGAGTT[-/A]AAACAAACAGATAGA | 57630 |
| rs745779860 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211348 | TTAGCTGGGCGTGGT[G/T]GCAGACGCCTGTAGC | 57630 |
| rs745783388 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195915 | GTGCAGTGGTGCAAT[C/T]TCGGCTCACTGCAAC | 57630 |
| rs745794329 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250747 | ATTTTAGACAGACAT[-/A]AGTGCCATGAAGAAA | 57630 |
| rs745800651 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241853 | CTTGAGATTTCCCTC[C/T]TCTCTGGCCCTTATG | 57630 |
| rs745852453 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096068 | ATGCATTCACTCTAT[G/T]TCAAAACGAATCTCT | 57630 |
| rs745882107 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227676 | CTACAATTACTCTCT[C/G]TGTGTGCCTTTCTCT | 57630 |
| rs745900126 | snp | G/T | 1.75047e-05 | 0.00295839 | missense | SH3RF1 | GRCh38.p7 | 4:169269188 | CCGGACACTCCAAAA[G/T]ATCCAACAAGGCTGA | 57630 |
| rs745903314 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213003 | TGTTATAAATATCCA[C/T]GTGCAGGTTTTTGTA | 57630 |
| rs745938349 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134475 | AGCTATTCCCATTCT[A/G]AGCTGTCACTATTCT | 57630 |
| rs745938488 | snp | A/G | 1.6593e-05 | 0.00288031 | missense | SH3RF1 | GRCh38.p7 | 4:169116348 | GATGTGGGGAGTCCA[A/G]GGAGAACGGTCACTA | 57630 |
| rs745964401 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165916 | CATGGGGAATAGATG[A/G]GGATGAATCTTGAGC | 57630 |
| rs745995472 | snp | A/T | 3.82248e-05 | 0.00437161 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107237 | ATGAGCCTTAGTTGG[A/T]GAATGACAGTACTAT | 57630 |
| rs746006317 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239056 | TAACTGCACAGTGCC[A/G]TTCTGGGTCAATTCT | 57630 |
| rs746016462 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120162 | AATCAAAAATATTTC[C/T]GGATATTGTCAAATG | 57630 |
| rs746041101 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154899 | TAATACAACTATGTG[A/T]CTACACATACTCTCT | 57630 |
| rs746054679 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167430 | TTACTCTTCAATCTA[-/C]CCCTCTTAGGTATTA | 57630 |
| rs746084175 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233057 | AGTTCAAGACCAGCC[C/T]GGCCAACGTGGCAAA | 57630 |
| rs746107590 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246516 | TACGTGCCTAAAGGA[A/G]AAAGTAGAAAAAGAT | 57630 |
| rs746112950 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142228 | CCCACAGTGCTGGCA[C/T]TACAGGCGTGAGCGA | 57630 |
| rs746126665 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249677 | TCCCCCCGTTGGAGA[C/T]ACACAGAGCAACAGT | 57630 |
| rs746136050 | snp | A/G | 1.76002e-05 | 0.00296644 | missense | SH3RF1 | GRCh38.p7 | 4:169156408 | TCTACCTTTACCTTT[A/G]CAAATGGAAGGCAAT | 57630 |
| rs746191724 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236413 | AATCCACACAACGTA[A/T]ACCTTGAGTGAGAAA | 57630 |
| rs746245904 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147614 | GGAGGAATTTTCGCC[C/T]CACAAATATGTGAAG | 57630 |
| rs746265913 | snp | A/G | 1.65411e-05 | 0.00287581 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117499 | CCTTTATCCTGATAT[A/G]TTCTGGCCTGGGTTC | 57630 |
| rs746266320 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206675 | GCCCCAAGCTAACAG[C/G]ATACCTTGGGTGCAT | 57630 |
| rs746272206 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098732 | CAGCGGGAGAAACAC[C/T]GGCCTAAGGATTGAC | 57630 |
| rs746280011 | snp | G/T | 3.42108e-05 | 0.00413573 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096481 | TTGTGCTACTTTGTT[G/T]TGTGAAGTGATTTTA | 57630 |
| rs746281748 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237306 | CATTAATTTTCCAAA[A/G]GTGACTTTCACCAGG | 57630 |
| rs746294767 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104761 | ACAAAAAAATTAGCC[A/G]GGCGTGGTGTGTGCC | 57630 |
| rs746297639 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253592 | ATGTGCATGTTGCCT[C/G]TCATAGGATTCAAAA | 57630 |
| rs746338300 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199977 | AAGATCGACATCATG[-/A]AGAAAATATTCCAGG | 57630 |
| rs746341118 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177983 | TTTTTGGTTGGGCAC[A/G]GTGGCTCATGCCTTT | 57630 |
| rs746342690 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136858 | TTGCAAGACTGAAAG[A/C]GTAAAAGACAATTTT | 57630 |
| rs746390929 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220522 | GGAGTGGGGAAGGTG[-/T]TTGTGGGTGGGGAAC | 57630 |
| rs746392259 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230074 | AGCCAGGCGTGGTGG[C/T]GCATGCCTGTAATCC | 57630 |
| rs746407493 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257464 | TCAAAAATGTCCCAG[A/G]GTAGAGGATAAACGA | 57630 |
| rs746422087 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133429 | GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC | 57630 |
| rs746456768 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248537 | CAAATACCTAATGCA[C/T]GCCAGGCTTAAAATC | 57630 |
| rs746456925 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179610 | TCCCACTCTCTTCAG[A/G]TTATATACGGATAAC | 57630 |
| rs746468352 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101763 | CTTTGAACAAAGCGC[C/T]GTGGAGGCATTATGG | 57630 |
| rs746482963 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116059 | GTTTAAACACAGAGA[A/C]ACATGAGCTCTAGAT | 57630 |
| rs746570204 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176550 | TGAGGGTTTTGTTTG[G/T]TTTTTTTTGAGACAG | 57630 |
| rs746572882 | snp | A/G | 2.83499e-05 | 0.00376486 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130166 | ATGAACCTGCCGAGA[A/G]AAGAAAAGTTATTAA | 57630 |
| rs746576908 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266094 | ACTGATGGATTCCCA[C/T]GGTGATTCCAATCCC | 57630 |
| rs746597044 | in-del | -/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272582 | AGTCCAGTTTGCAAA[-/C]TGAAAGTTACTACTT | 57630 |
| rs746599055 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126304 | AGAGGTCTCAGTTCC[C/T]GAGATGCTAGAATCC | 57630 |
| rs746609576 | snp | A/G | 1.6498e-05 | 0.00287206 | missense | SH3RF1 | GRCh38.p7 | 4:169269091 | TCATTTCGAGAACCT[A/G]CGATCCCCAGCAAAC | 57630 |
| rs746621091 | snp | C/T | | | missense | SH3RF1 | GRCh38.p7 | 4:169136343 | GCACTGCAGGAGAGC[C/T]CAGACAGCTCGCTGA | 57630 |
| rs746628451 | snp | A/G | 1.70904e-05 | 0.00292316 | missense | SH3RF1 | GRCh38.p7 | 4:169130089 | GATGGGAAAGTAAAC[A/G]AGGGGCCAGTTGTCA | 57630 |
| rs746652375 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154021 | ATCAGCATGTAATAT[C/T]GATAATACCTAAAAA | 57630 |
| rs746656935 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230003 | TTGAGGTCAGGAGTT[C/T]GAGACTAGCCTGGTC | 57630 |
| rs746673548 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216521 | TTTACTACCATGGAG[C/T]ACATAAATGTCTGTT | 57630 |
| rs746677567 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222913 | TGAAGCCAAATGGGC[A/G]GCTATAAATGCCTGT | 57630 |
| rs746696143 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267165 | ATGTTAGCAAGAAAA[C/T]TTAAAATTCAAAAGA | 57630 |
| rs746722562 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122411 | GGGCAGAATCAGCAG[A/G]CTAACTGATATGAAA | 57630 |
| rs746764171 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268179 | CAAATCCCAAGAAAA[A/T]TCATTTCGATGGAAA | 57630 |
| rs746779252 | in-del | -/TTGA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149806 | AGTTCAATCAACTCT[-/TTGA]TTATTAGATCAAAGG | 57630 |
| rs746788526 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094980 | GTGGTAAGGATCTTA[C/T]TCATTACCAGGCTGT | 57630 |
| rs746792294 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129964 | TATGAACATACGCTG[C/T]AGGTGTTAGGAGGTG | 57630 |
| rs746794115 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108685 | TGTCCTCAGCTGATC[C/T]TATGCGCTTTCGCTT | 57630 |
| rs746804488 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143516 | GGGTGGCTGTGCTCC[C/T]GAGGCTCATTAAGCA | 57630 |
| rs746812458 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188533 | TTAAGAAACGATACA[C/T]TGCTTTTCTCTAATT | 57630 |
| rs746867781 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | SH3RF1 | GRCh38.p7 | 4:169120975 | CGAGGAGTGTATGGA[C/T]ATATAGCAACATACC | 57630 |
| rs746876789 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096378 | TCGCTGGGGTAACTG[G/T]GCTGGGGCATCAGAG | 57630 |
| rs746879139 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175055 | TTGGTAAATAGCCCA[C/T]TGTTCACCTCGTTGC | 57630 |
| rs746894398 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129164 | GGCAGGGTGATGCAA[C/T]TGGTGTAGGTACTAG | 57630 |
| rs746963721 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114470 | CCATGTAATGAAACA[C/T]CTTTAAAAGTTCCAG | 57630 |
| rs746965079 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162093 | AGGCAGTAGGCAGAG[A/G]TTGCAGTGAGCCAAG | 57630 |
| rs746970640 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166908 | ACATCTTACTGTTGC[C/T]TACTTCAAGAAGAGG | 57630 |
| rs747012291 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237249 | ACACACGGTGAAGGT[A/G]ATTTGAAAGTCATAC | 57630 |
| rs747013337 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100847 | TAAGCCTGAACATGT[C/T]CCCTATTCAGGGCCT | 57630 |
| rs747035534 | snp | C/T | 5.49637e-05 | 0.00524202 | missense | SH3RF1 | GRCh38.p7 | 4:169136424 | ATCTCCATGGAGTGG[C/T]GGTTCTGGGATGCCT | 57630 |
| rs747060342 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225083 | TAAAGAGAGCAAAGC[A/T]CTGCATTGATGAATT | 57630 |
| rs747061558 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098685 | CAAGGCTGGGGTTTG[A/C]TCAAGCATGGAATGA | 57630 |
| rs747084987 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268695 | TCAGAGGTATAATCT[A/G]TCTGTTCCAGTATGT | 57630 |
| rs747103061 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206388 | ATCCATTCAAGGGGC[-/T]TGGGGGAAGGGGGGT | 57630 |
| rs747104988 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177875 | ATATATATATGCTCA[C/T]GTTATACATACACAT | 57630 |
| rs747130698 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133245 | ATAAAAATGAATACT[A/G]ACATTTTTAAGCCCC | 57630 |
| rs747131702 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243761 | TTTCATTTACTGTTT[A/C]CCTATTTGAACTTTT | 57630 |
| rs747155312 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164696 | ACACTGGAACTAAAA[C/T]ATAGTCCGTTCTGGA | 57630 |
| rs747190921 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094872 | CTTGTCATTGCAAGA[C/T]TTTTCAGTTCATGTT | 57630 |
| rs747191027 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179432 | TGTAGTTTTAAGCCA[C/T]TGAATTTGTTGTAAT | 57630 |
| rs747225100 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212887 | TAACTTCTGGCAACC[A/G]CTGATCTTTTTACTG | 57630 |
| rs747241161 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153862 | CTTTCCAACTTAAGT[C/G]AGAGTAAATAATCCT | 57630 |
| rs747244062 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243956 | CATGGCAAGCTACCC[G/T]GGAGTTGCCAAAGTC | 57630 |
| rs747262671 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262353 | CATTTTGAAATCTAC[A/T]TTCTTTCTCATTTTA | 57630 |
| rs747264084 | snp | C/T | 1.65627e-05 | 0.00287769 | missense | SH3RF1 | GRCh38.p7 | 4:169116364 | GGAGAACGGTCACTA[C/T]CCGGCCACTGGGCTC | 57630 |
| rs747281765 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217656 | TCCTGGCTAGCTGAG[A/C]ATCAGATATGAGGAA | 57630 |
| rs747299976 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165865 | CTGAGAAAAATAAAG[G/T]CTTTTCAAAAGATGA | 57630 |
| rs747336582 | snp | C/T | 3.29554e-05 | 0.00405914 | missense | SH3RF1 | GRCh38.p7 | 4:169156543 | AAGCCATGGATTCCA[C/T]TGACTTCCCCATGGT | 57630 |
| rs747342054 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248032 | GAAATGCTTTTACAC[C/T]GTTGGTGGGACTGTA | 57630 |
| rs747343511 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137789 | CTTCCTCACAAAGCC[A/G]TGTTAACTGGAGCTC | 57630 |
| rs747367743 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203625 | AACAAGAATTTCCTT[A/C]TGTAAGTGTATGGAA | 57630 |
| rs747377724 | snp | C/G | 1.78688e-05 | 0.00298899 | missense | SH3RF1 | GRCh38.p7 | 4:169106868 | CAAACGACAGGTCTA[C/G]ACTCATTCAAGACAG | 57630 |
| rs747396242 | snp | C/T | 1.72255e-05 | 0.0029347 | missense | SH3RF1 | GRCh38.p7 | 4:169156427 | ATGGAAGGCAATCTT[C/T]GTCTGCTTCCTTGTC | 57630 |
| rs747410432 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256043 | AAAGTTCTGAGACTA[C/T]AGGCGTGAGCCACCA | 57630 |
| rs747453732 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271180 | GCCACCCGCCGCCGC[A/G]CCGGCCTCCCGCGCT | 57630 |
| rs747454085 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125209 | TTGGGGTCAAAAAAA[A/C]ACATAGATTCCAACC | 57630 |
| rs747466121 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158560 | ATGCACAAACAGACT[C/T]AGGTCCTATGTGCCG | 57630 |
| rs747531998 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205583 | CCTTCTTGGGTTCTT[G/T]TTTCCCATTTGCTCT | 57630 |
| rs747545787 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269978 | CATTTCTGAACGGCC[C/T]GTCCTAATCCCATTC | 57630 |
| rs747549693 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207058 | TGATCTCCCAGGCTC[A/C]AGCTATCCTCCCACC | 57630 |
| rs747572515 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108478 | CAGTGCACCATAGTC[C/T]CCAGTTACCTAACGC | 57630 |
| rs747577929 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176691 | GATTACAGGCATGCA[A/C]CACCATGCCTGGCTA | 57630 |
| rs747581369 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111645 | ATTTGGAGACACATT[C/T]TCCTGGAGATTAGTT | 57630 |
| rs747582275 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113468 | TGGGAAATTCTAAAA[C/G]AGTATTAAACAAAAG | 57630 |
| rs747642325 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264782 | GGCAGTTCTTGATGC[A/C]TTCTACATTATCAAA | 57630 |
| rs747721685 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208238 | CCCCAAGTAATAGCC[A/G]TTTCTGTCCAGAGTT | 57630 |
| rs747729613 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263916 | TTAAGAAATTATGCC[A/G]GGCAATGTGGGTAGT | 57630 |
| rs747760701 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249838 | ATTTCAATGAGTTGT[A/G]CATATAACCCATACA | 57630 |
| rs747761173 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133056 | CCTTTCACCTTCCAG[C/T]TGCCAGCAATTTGGA | 57630 |
| rs747767546 | in-del | -/CAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126613 | TGTTTTTTTTAGGAA[-/CAG]CAGCATCTAGTCCTG | 57630 |
| rs747778143 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226695 | TTTTATAGGAAACTA[C/T]TGTAGATAATAAAAC | 57630 |
| rs747790343 | snp | A/G | 1.78704e-05 | 0.00298913 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136375 | CCGTGCAGCAGCAGT[A/G]GGGTTGCTGGAGCTG | 57630 |
| rs747814364 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130445 | AACACATTGCCTCAT[C/T]TGGTACGCCACCATG | 57630 |
| rs747818766 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195239 | TTAAAGATGTTGTTC[C/T]ATTGCCTTCTGCTGG | 57630 |
| rs747831872 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197464 | AACCCCGTCTCTACT[A/G]AAAACACAAAAATTA | 57630 |
| rs747837862 | snp | C/T | 3.29783e-05 | 0.00406055 | missense | SH3RF1 | GRCh38.p7 | 4:169117528 | TCCTCCTTACCTGTC[C/T]TCACAGCATTGCGGG | 57630 |
| rs747872762 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180835 | TAGACACTTATTCTT[C/T]AGGCTTTTTAACTCT | 57630 |
| rs747885188 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134868 | GTACAAAACAAAGAC[A/C]CTTGCCTTCACTGCA | 57630 |
| rs747898062 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231818 | AATAGTCATCAAATA[C/G]CTACTACATGTCAGG | 57630 |
| rs747922002 | snp | A/T | 1.67133e-05 | 0.00289074 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130191 | TATTAAAAAGAAGAC[A/T]ATGTTTAATACAACA | 57630 |
| rs747947397 | in-del | -/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103088 | ACCGCGCCTGGCTAT[-/TT]TTTTTTTTTTTTTTT | 57630 |
| rs747984468 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232975 | TAAACTGGGCCAAGC[A/G]CAGTGGCTCACACCT | 57630 |
| rs747992817 | snp | C/T | | | missense | SH3RF1 | GRCh38.p7 | 4:169106983 | CCTGGGCCAGGGCTG[C/T]TCCTGCCACTGCAGT | 57630 |
| rs747994379 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184630 | TGAGCCACTAAAAAG[C/G]AGATGCCAATCACAG | 57630 |
| rs747997756 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199845 | AACATTCAGCAAGCA[C/T]GACACATGTAAATTA | 57630 |
| rs747998725 | snp | C/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271678 | CGATGGGGACAGTGC[C/G]GCGGCCACCTGTCCG | 57630 |
| rs748011254 | in-del | -/CTAT | 1.87078e-05 | 0.00305836 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116667 | CACAGCAAAATTCAA[-/CTAT]CTAATAGATGCTGCT | 57630 |
| rs748011537 | snp | A/C/G | 3.29974e-05 | 0.00406175 | synonymous-codon, missense | SH3RF1 | GRCh38.p7 | 4:169268928 | CTGAGACCTTAATGC[A/C/G]TTTGTGCAGTTGGTC | 57630 |
| rs748016834 | snp | A/T | 1.67913e-05 | 0.00289748 | missense | SH3RF1 | GRCh38.p7 | 4:169116319 | TCCCACAAGCTGATG[A/T]AGCACTGTCAGGAGA | 57630 |
| rs748055724 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118109 | CCTTCATCTACAGAA[-/C]CAAGCTAGGATCATT | 57630 |
| rs748060723 | snp | C/T | 5.71293e-05 | 0.00534428 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107227 | AAAAAAAATAATGAG[C/T]CTTAGTTGGAGAATG | 57630 |
| rs748070376 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221316 | CATCTGAATGTAAAA[A/G]AAAAATAGGTCTCTC | 57630 |
| rs748086229 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172152 | CCTAAGAAAGCAAGA[A/G]CTGAAAACATATTAT | 57630 |
| rs748093400 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173322 | TAATTGACTCAGGCA[C/T]CTTAACAAAATATTA | 57630 |
| rs748104100 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173071 | ATTAAGATATACAAA[C/G]AGGAGTAATAATAAA | 57630 |
| rs748122213 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127691 | CCTAAAATAAAATGG[C/T]TGAATGTAAATTAAT | 57630 |
| rs748124972 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147053 | TTTGGAGCAACAGAT[A/G]TACAGTCTATTCATG | 57630 |
| rs748130523 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250893 | GAAGGAAAGGAGCAA[A/G]CCATGTTGAGACCTG | 57630 |
| rs748134283 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248568 | TAGATGATGGGTTGA[C/T]GGGTGTAGCAAACCA | 57630 |
| rs748155943 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203121 | AATTATTTGACCAAA[C/T]GTCTCACAGAAAACA | 57630 |
| rs748162811 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095413 | ATCTTAACAGGAAAT[C/T]GCAATGAAATATACA | 57630 |
| rs748170929 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158423 | TGCAGTATTCCTGGA[G/T]AAGAATTACGGAACA | 57630 |
| rs748194069 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235229 | GTACCCAAGTATCAT[A/C]TAGCTTACATAACAA | 57630 |
| rs748216220 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097093 | GGAGAAGTAGCTGAG[C/T]AGGGGGGGTTCAGTC | 57630 |
| rs748283925 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236315 | TGCCAATTCCCTTCC[C/T]GGAAGCATGTGCTGA | 57630 |
| rs748286197 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223741 | CAGGTTGTGATAAGC[A/G]CAAATAAAAATAAAC | 57630 |
| rs748289681 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176466 | TGATCAATTTTAACC[A/G]AACAAAACAAATATT | 57630 |
| rs748295102 | in-del | -/GCAAAAGCAACCAACAAAC | 1.79314e-05 | 0.00299423 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136623 | CAGCCGAGTTAAACT[-/GCAAAAGCAACCAACAAAC]CAACACAAGAAGGTT | 57630 |
| rs748303279 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130979 | AGAAGCAATGTGGTT[A/G]GCTGGTACCTGCCTC | 57630 |
| rs748306217 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097744 | CTTGTGTAGTCTCCT[C/G]CTATGATGCACAGGA | 57630 |
| rs748324197 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237087 | AAAGAGATTCAACAG[-/A]AGGAGCCAAAAATGT | 57630 |
| rs748371988 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224942 | ATCGAGTCTCATTCT[C/G]TAACAGGGTGCCCAA | 57630 |
| rs748389835 | snp | A/G | 3.31477e-05 | 0.00407096 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116452 | GGCCAGAGGGGCACT[A/G]GCTCGACTGATACTG | 57630 |
| rs748395378 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131850 | GGCCAAGTCTTTGTT[A/T]GCATAGAAGTGCAAC | 57630 |
| rs748412049 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228908 | TAATTTTGTAATGTT[A/C]GAATTTTACTTTAAA | 57630 |
| rs748438787 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102538 | TTTTTTTTCTTTGGA[A/T]GAAAAACCTGTCATA | 57630 |
| rs748448391 | snp | A/G | 2.00178e-05 | 0.00316362 | missense | SH3RF1 | GRCh38.p7 | 4:169122214 | CCTGGTGGTGTGGAG[A/G]CAAGGACAGTGGCAG | 57630 |
| rs748459340 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136226 | CAGAAGTTCAAAATA[A/G]GCAATGTTTGTCAGC | 57630 |
| rs748485389 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261605 | AAGTGAGACCATCTC[-/A]AAAAAAAAAAAAAGA | 57630 |
| rs748533008 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268280 | GTTGCTACAGCAACG[A/G]AACTCTGCTACCTGT | 57630 |
| rs748567016 | snp | C/T | 1.66136e-05 | 0.00288211 | missense | SH3RF1 | GRCh38.p7 | 4:169122168 | CATGGGCCTCGGTCC[C/T]ATTCCAGCAGCAGCA | 57630 |
| rs748620346 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113752 | ATTTATATCAACCAG[A/T]AGTCTCTTTAGTGGA | 57630 |
| rs748622093 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156566 | CCCATGGTACCAATT[C/T]TCATCCACTTGTCTT | 57630 |
| rs748625213 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168996 | CAAAGTCTGTCATGA[C/T]CTTCTACAATGTCAT | 57630 |
| rs748676238 | snp | A/G | 1.68809e-05 | 0.0029052 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106957 | GGAACTTGCCTTCCT[A/G]TGAAAAGCATCCTGG | 57630 |
| rs748696185 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220190 | TTATAAAATGTGCAT[A/G]ATTTTGACTGCTTTA | 57630 |
| rs748696773 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108807 | CAGTGCTGTATATAC[A/C]TCTCTATCTCACCCA | 57630 |
| rs748723842 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123575 | TGGCTCACATTCTCA[A/G]TTCAAAATATGGCAC | 57630 |
| rs748736318 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157328 | TTATAATCTGTAAGT[A/G]TATAGACACGTGGTC | 57630 |
| rs748774878 | snp | A/C | 3.55366e-05 | 0.0042151 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156716 | GAATTTTAATAAAAT[A/C]ATGGTCTTAAAATGT | 57630 |
| rs748778970 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232885 | GAACATATAATCTAC[C/T]AGTCTACTGATCGGT | 57630 |
| rs748816924 | snp | C/T | 3.29636e-05 | 0.00405964 | missense | SH3RF1 | GRCh38.p7 | 4:169156607 | TGATGTCACCTTTGC[C/T]GAATTTAAGGTCTCC | 57630 |
| rs748848993 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196817 | ATAAGCTGTTCCTTT[-/A]CTATATCACCTTAAA | 57630 |
| rs748883953 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112035 | TTATATTTCTCTGTG[C/G]AACAGCAGCAGTAAC | 57630 |
| rs748897560 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227251 | TAACAAAAATCATTA[C/G]ACTATAACATCAATC | 57630 |
| rs748902100 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173129 | GACTTGAGAAATAAA[A/G]CATTATAAATGCAAT | 57630 |
| rs748913848 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127247 | TAACTTCGTTCTGCA[G/T]AAAAGATTTAAAAAT | 57630 |
| rs748915128 | snp | C/T | 1.67385e-05 | 0.00289292 | missense | SH3RF1 | GRCh38.p7 | 4:169117757 | TAGACATAGGGACTT[C/T]AGCTTGGGAAGCATT | 57630 |
| rs748930538 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159845 | AATGCAAAGAATGTT[C/T]CTCCTAGGAAGTGTT | 57630 |
| rs748941504 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160992 | CATGTCATCACTGGG[C/G]CCTCTGCCCTCCAAG | 57630 |
| rs748957317 | in-del | -/AAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119637 | TTTTAACATACATAG[-/AAA]AGAATGTTTATATTG | 57630 |
| rs748970491 | snp | A/G | 1.72273e-05 | 0.00293485 | missense | SH3RF1 | GRCh38.p7 | 4:169106901 | CCCAGGGAGGAACAG[A/G]CCTGGCGAGGAGGTG | 57630 |
| rs748973872 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255384 | TTATATCTGTTTATA[C/T]ATGTCACAATTTTTT | 57630 |
| rs748973894 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113403 | GTGTAAGCCACCGCG[C/G]CCGGCCCCAATTTTC | 57630 |
| rs748979217 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237383 | CGATGGCTCATGCCT[C/G]TAATCACAACACTTC | 57630 |
| rs748990053 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104251 | AATGAGAGGGAACAC[A/G]GGAGAGATGCCCTCA | 57630 |
| rs749009819 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148855 | AAGAAATATCCCTGA[C/T]GAGCTGTAAAGAGAG | 57630 |
| rs749027506 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250696 | GGGTAGTGGGGATGG[C/G]GGTAGGAGGGATTAA | 57630 |
| rs749046864 | snp | C/T | 3.2963e-05 | 0.00405961 | missense | SH3RF1 | GRCh38.p7 | 4:169117642 | GCTGCGGGGACAACA[C/T]TGGGACTCCCAGCCA | 57630 |
| rs749047125 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242320 | CGACCCATGTTCTAA[C/T]ATCTTTGTAATTTTT | 57630 |
| rs749092405 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150253 | TGAGGATCCTTGACA[A/G]TAAGTCTGTCCTACC | 57630 |
| rs749094002 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241836 | TGCTCGGTAAAGTCA[A/G]CCTTGAGATTTCCCT | 57630 |
| rs749100352 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152840 | TCCACAGTCACATGA[C/T]GTTGAGGAAGAAAAG | 57630 |
| rs749110676 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222513 | TTTTATACATATTTA[-/TA]TATATATATATAAAT | 57630 |
| rs749134472 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243551 | AATAAATAATAAAAT[C/T]AGAACTGGATAGAAT | 57630 |
| rs749140909 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123023 | TTAGGGTCTGTATAC[G/T]GAAACTCTTGGGAAA | 57630 |
| rs749141906 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198237 | TACTGTGGCTTTCAA[C/T]ACTTTAAACCACAAA | 57630 |
| rs749147693 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173355 | ATGACATTAGTAAAA[C/T]TCCCACCGTGCCCCC | 57630 |
| rs749161559 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199395 | CGTTCAAAGACTCGG[A/G]TTCTTACCATCTTGT | 57630 |
| rs749166538 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104585 | ACTATAGAAAATTAT[G/T]GTACAGCACTATAAA | 57630 |
| rs749175843 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264731 | CACTTCCTATCTATC[C/T]TACCCATCTGACCCT | 57630 |
| rs749184584 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231519 | TGCAGTGAGCCGAGA[C/T]TGCACCACTGCTCTC | 57630 |
| rs749186988 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105642 | CTCACGCCTGTAATC[A/G]CAGCATTTTGGGAGG | 57630 |
| rs749187820 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153687 | CTACCAGGAAGTTCA[A/G]TCTGATGGCTTGACA | 57630 |
| rs749193020 | in-del | -/AAAAAATAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169597 | GCAAGACACTGTTTC[-/AAAAAATAAA]AAAAAATAAAAAAAT | 57630 |
| rs749205602 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183194 | AATCTCAACTACTAG[A/G]GAGGCTGAGGCTGGG | 57630 |
| rs749233629 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139909 | CTCTTTTAGCTCTCC[A/G]CATGTATAATGCATA | 57630 |
| rs749248619 | in-del | -/ATT | 1.82154e-05 | 0.00301784 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136652 | AAACCAACACAAGAA[-/ATT]GGTTAAACAATTCCT | 57630 |
| rs749264440 | snp | C/T | 1.65048e-05 | 0.00287265 | missense | SH3RF1 | GRCh38.p7 | 4:169120987 | GGATATATAGCAACA[C/T]ACCTAGAATAGAAAA | 57630 |
| rs749293403 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184499 | ACTTCCCTGAGTCTC[A/C]CAGGAGGATAGCTAT | 57630 |
| rs749310752 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236001 | AATTTCTTTCAGTGA[C/T]ATTTCCTCTGCAACC | 57630 |
| rs749319146 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270319 | ACACACCCCGGGGCC[-/A]GGTGTCGGCGGCACC | 57630 |
| rs749331412 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201133 | AAATTTAAAATATAC[A/G]ATCAATATTTTTAAA | 57630 |
| rs749340377 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109920 | AGCCTGAGGTGGGAG[A/G]GAGGGTTGCTTGAGC | 57630 |
| rs749349657 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122075 | AATGAACACATAAGC[A/G]GTAACAGACGACACG | 57630 |
| rs749360946 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107873 | CCTCCTTGATTAGAC[A/G]TCCATTTTAAGGAAA | 57630 |
| rs749364518 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166759 | AGAGAATGGTTTTCC[C/T]GAAGCAGCTGGCTAC | 57630 |
| rs749371517 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259334 | TTCATGTTTCACAAC[A/G]CAAATAATCTACTAT | 57630 |
| rs749376857 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156010 | CCATTTTATCAATTC[A/G]GCAGATATATTCCTG | 57630 |
| rs749388246 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108713 | CTTCACTCATTCAAT[A/G]CCACATTTTCCGTGG | 57630 |
| rs749431828 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247688 | CGATCTGAGTCTGAG[C/G]AGGCATCATGACATT | 57630 |
| rs749431839 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234214 | AATTGTCCCACTTGG[G/T]ATAATTAATCGGGAG | 57630 |
| rs749437800 | snp | A/G | 1.65004e-05 | 0.00287227 | stop-gained | SH3RF1 | GRCh38.p7 | 4:169155554 | TTTCATCCACTCTTC[A/G]GATCACAGTCAGAAC | 57630 |
| rs749446739 | in-del | -/CTGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177660 | TCAACTATGTGTTAA[-/CTGT]CTGATCTACTAATTT | 57630 |
| rs749446964 | snp | C/G | 1.64871e-05 | 0.00287111 | missense | SH3RF1 | GRCh38.p7 | 4:169120876 | TTGCTGGTATGCATG[C/G]ATGTCCCTTTGAACC | 57630 |
| rs749451347 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188694 | AAGCTTTCTGGCTTA[C/T]GTAACAATTTCAACC | 57630 |
| rs749453857 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257707 | AGACAATCTCTAATT[A/G]TTGGAATTTCAAGCA | 57630 |
| rs749461234 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114506 | AGGAGGTGGACATCC[C/T]TGGGGAGTCACTATT | 57630 |
| rs749464699 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156897 | TACGACACCCATGCA[C/T]CAGCCATGATTTAGG | 57630 |
| rs749467882 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222850 | CTTCCAATACATGAG[C/T]TCAGCTAAGAAAACT | 57630 |
| rs749492724 | snp | A/G | 1.81764e-05 | 0.00301461 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136646 | AACCAACAAACCAAC[A/G]CAAGAAGGTTAAACA | 57630 |
| rs749519632 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234889 | ACGCACAGCATTTCT[A/G]GCTTCTACCCACGAG | 57630 |
| rs749524260 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143368 | ATGTCTTTGAAACCC[G/T]GTGCGAACGGAGTGC | 57630 |
| rs749589112 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175244 | TCAACACCATCTGTA[C/T]TGCCACTATTAACAC | 57630 |
| rs749613025 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250230 | AGTACACCAATGCTG[C/T]CAGTTATAAAGGATT | 57630 |
| rs749630409 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266249 | AGGAGGCCACATGGT[C/G]ACAGCCTAACCAAAC | 57630 |
| rs749637921 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179697 | GCAAAGACAACACTG[C/T]GCAAACTTTGAGTAA | 57630 |
| rs749699831 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227760 | TAGAACAGTGCCCAT[A/C]GAAGCCAGACCCAGT | 57630 |
| rs749703738 | snp | C/G | 1.76284e-05 | 0.00296882 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169130052 | TATACTCACTCCAAG[C/G]GCAGCTTGGTAGGGA | 57630 |
| rs749704174 | snp | C/T | 6.73446e-05 | 0.00580239 | missense | SH3RF1 | GRCh38.p7 | 4:169116534 | GAGGCCAGCGAGTGA[C/T]GGGACAGGCCCACAG | 57630 |
| rs749746951 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130907 | TACTAGAAGCTACAG[A/G]AGTAGGGGGATGGGT | 57630 |
| rs749756406 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159576 | CGCTGTGCCTCTTTC[C/T]TCATTTGGGCTGTTG | 57630 |
| rs749766172 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156750 | TGAAAATACAACTGC[A/G]TTGTCATTGTTTTAA | 57630 |
| rs749771410 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253075 | AGGAAAAGTTTGGAT[A/C]GCAAAGAAGAAACTT | 57630 |
| rs749775225 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180720 | ATCGTTAAAAAAAAT[A/T]ATATTTATATCAGAT | 57630 |
| rs749787787 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228580 | GCCCCAGTGATTACA[C/T]TGGACTCATCCAAAT | 57630 |
| rs749789870 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214625 | GTAGTTTTCCTTGCA[C/G]AGATATTGCATGTTT | 57630 |
| rs749831467 | in-del | -/GGG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147480 | ATGTGCATGGGGGCA[-/GGG]TGGGGGAATGGTGAT | 57630 |
| rs749836716 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226979 | TGAGACCACCCTGGT[C/G]AACATAACAAGACCC | 57630 |
| rs749837412 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136051 | ATTGCTTGGTGAAAC[A/T]GGTAAGTATTATATA | 57630 |
| rs749837495 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120389 | TATCTCTGTGCCTCA[A/G]TGTAACAGCAACTAA | 57630 |
| rs749884027 | snp | C/T | 1.77681e-05 | 0.00298056 | missense | SH3RF1 | GRCh38.p7 | 4:169116276 | GGTCTTACTTTGCTA[C/T]CCTTGTCTGGTTTGG | 57630 |
| rs749924349 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234349 | TTATTCAGTCTAAAA[C/T]GTCAAGAGTGTGAGG | 57630 |
| rs749928358 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270734 | CCACGGGGACCCGAG[A/G]GCGAGGGGAGAGAGA | 57630 |
| rs749930053 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117905 | AAAAAATGAATGGAA[G/T]TATTTTTATAAAGTT | 57630 |
| rs749945252 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244588 | CTAACTATAACCAGC[A/G]CTGCTTGGCAGAGAA | 57630 |
| rs749945349 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266156 | GAAACACTAAAATTT[G/T]GGGAACAAGATGTGC | 57630 |
| rs749967806 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119407 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 57630 |
| rs749987085 | snp | A/C | 1.77143e-05 | 0.00297605 | missense | SH3RF1 | GRCh38.p7 | 4:169107190 | AAAGCAACTTCAACA[A/C]ACCCTTTTTTTCTTT | 57630 |
| rs750046963 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184355 | TCCAAATAGATCTCA[A/G]CTTCCACACTTGAAG | 57630 |
| rs750082191 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236986 | TTGCTTCTGTCTCAT[C/T]CCCTGCCAGTAATAC | 57630 |
| rs750082982 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245693 | CCAGAAATACAGCAA[A/G]TTCAGCTGATAGAAA | 57630 |
| rs750094489 | snp | A/G | 1.64781e-05 | 0.00287033 | missense | SH3RF1 | GRCh38.p7 | 4:169120924 | TCAAACACTAAAAAC[A/G]TCTCCCCTTTTCTCA | 57630 |
| rs750115352 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106550 | AGAAAGAAGTAAATC[C/T]ATGAACAGTTTCCCA | 57630 |
| rs750121763 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155290 | AAAAGTAAAGAGTTT[C/G]AAGTATCTCACTGTC | 57630 |
| rs750138005 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104901 | TGAGACTCCCATCTC[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs750188875 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249177 | AGCTTGCAGTGAGCC[A/G]AGATCGTCCCACTGC | 57630 |
| rs750191002 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236003 | TTTCTTTCAGTGACA[C/T]TTCCTCTGCAACCTA | 57630 |
| rs750214945 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147287 | CAGATGTAGGGATAC[C/T]ATAAAAGAAATATAC | 57630 |
| rs750217579 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | SH3RF1 | GRCh38.p7 | 4:169096565 | AGGCCAGTTTTCCCA[C/T]TACGTTGTAATGTGC | 57630 |
| rs750224480 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224755 | GCTTGGCTTGGGTAG[A/G]TGCTCAGATGTAATA | 57630 |
| rs750271876 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131527 | CCAACCTATTTCTAA[C/T]GGGAAGCACACTGGT | 57630 |
| rs750276255 | snp | C/G | 1.78446e-05 | 0.00298697 | missense | SH3RF1 | GRCh38.p7 | 4:169136613 | AGCTGCTTAGCAGCC[C/G]AGTTAAACTGCAAAA | 57630 |
| rs750278998 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236845 | AGGCTAACAAATAAT[A/T]CACTGACAGACACAA | 57630 |
| rs750303135 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148036 | ATAAAAAGGCAACCT[C/T]AGATATTTAAAATTG | 57630 |
| rs750338551 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192052 | AAATAGCTGGGACTT[A/G]ATTATACTAAAGAGC | 57630 |
| rs750350244 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177500 | CACACTGACTTTAAT[A/G]AGCACACAATAAATT | 57630 |
| rs750382070 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156269 | AGACTGCTTCTAGGC[A/G]TTTTCAGAAGCATAG | 57630 |
| rs750383598 | snp | C/T | 1.8014e-05 | 0.00300111 | missense | SH3RF1 | GRCh38.p7 | 4:169116592 | GTACCTGGATGGGTG[C/T]CACTGCTGCCGTGGG | 57630 |
| rs750421825 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251624 | ATTTAAGCCTTATTT[G/T]AAGGATTGTGAGAAA | 57630 |
| rs750424782 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101331 | GATGAACCTTGCAAA[C/T]GTTATGCTAAGTGAA | 57630 |
| rs750430252 | in-del | -/GACTCAAGCAATCCTCCC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174291 | CTCTCAAATTCTTAA[-/GACTCAAGCAATCCTCCC]GACTCAAGCAATCCT | 57630 |
| rs750447002 | snp | A/G | 1.66098e-05 | 0.00288177 | missense | SH3RF1 | GRCh38.p7 | 4:169156672 | GCACATGGTAACTGA[A/G]GTATACCCTTTAAAA | 57630 |
| rs750448247 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240154 | TTCAAAAGTCAATTA[A/G]AACTTCTCAAGGGGT | 57630 |
| rs750458182 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115429 | GGCATTAGATTCTCA[C/T]AGGAGCATGAACCCT | 57630 |
| rs750460686 | snp | A/T | 4.94923e-05 | 0.0049743 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122147 | AATCTGGTCAGTGGA[A/T]CCTGCCATGGGCCTC | 57630 |
| rs750469523 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251384 | TGAAGAGTATTGTTT[C/G]AGATAATCTCAGTCA | 57630 |
| rs750482673 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172599 | TTAAGGAGATGTGTA[C/T]GGGGCTAAGTTGACA | 57630 |
| rs750527577 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105585 | TTAGCCATACCCTTC[C/T]GGCTCAGGAAGAAGA | 57630 |
| rs750558489 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102193 | AAGTATTTCACTGGC[A/G]TAACCATACTAGTTC | 57630 |
| rs750579627 | in-del | -/A | 0.000206652 | 0.0101628 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268796 | CCACCTTTATTCACC[-/A]AACTACCTCTGTAGG | 57630 |
| rs750592537 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250625 | CCTGCTGGGGATACA[C/G]ACAGGAATAAATTTA | 57630 |
| rs750606012 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152246 | AAAGAATCTCCGGAG[A/G]GGAAGGGTGAATGTG | 57630 |
| rs750606925 | snp | C/T | 1.69424e-05 | 0.00291048 | missense | SH3RF1 | GRCh38.p7 | 4:169106932 | GAGCGATGGGAACTG[C/T]GGAGTCCAGGGAACT | 57630 |
| rs750627512 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229626 | TTCCTAACATCCCTA[C/T]AAATAACCTGGGCTG | 57630 |
| rs750646018 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243457 | GGCAGAGGTTGCAGT[A/G]AGCCAAGATCGTGCC | 57630 |
| rs750659487 | snp | C/T | 3.72086e-05 | 0.00431311 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106844 | GAACGAAGTTGAACT[C/T]ACCTTTCACAAACGA | 57630 |
| rs750686667 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121877 | TACAAAAGAGGCAGT[A/T]TCATACCCATATAAT | 57630 |
| rs750696562 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168362 | CCAGTCAGTCTCTCA[C/T]TAGATGTCCAGGATA | 57630 |
| rs750739676 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233370 | GTAGCATATATATCA[C/T]AAAATAATTACCAAA | 57630 |
| rs750757248 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220957 | TTCAAGGCAGAAGTT[C/T]AGCAGACAAACAATT | 57630 |
| rs750783750 | in-del | -/CAG | 0.00152904 | 0.0276076 | cds-indel | SH3RF1 | GRCh38.p7 | 4:169122172 | GCCTCGGTCCCATTC[-/CAG]CAGCAGCAGCAGCAG | 57630 |
| rs750796254 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187274 | TGTAATCTTGGCTCA[C/T]TGCAGCCTCCCAGGC | 57630 |
| rs750805140 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172958 | GGTTATGTATTTTCT[A/G]TCATGAACAGATATT | 57630 |
| rs750812210 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260328 | GCAGTTTTAGGAAGG[C/T]AATGGAGAAGGACTG | 57630 |
| rs750845775 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128752 | ATCTGGTCCTAAGCA[C/T]TCTAGCAGAGGGAAA | 57630 |
| rs750847190 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222023 | TGAACATCTATACAT[A/T]ATCAAGTGTAGGTGT | 57630 |
| rs750848323 | snp | A/G | 1.80624e-05 | 0.00300514 | missense | SH3RF1 | GRCh38.p7 | 4:169136337 | GAAGGGGCACTGCAG[A/G]AGAGCCCAGACAGCT | 57630 |
| rs750850432 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174148 | GGCTCACTGCAGCCC[C/T]GACCTCCGGGCTGAA | 57630 |
| rs750935857 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161753 | TATATCTAAATTGGC[A/C]TCAATGCTGGCTGAT | 57630 |
| rs750959505 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193827 | TACGAGCCTTGGGAA[C/T]AAATTAGCTGTTAAC | 57630 |
| rs750964730 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262788 | ACTTTTTTAAAAAAA[G/T]TATCAATTAGTATGC | 57630 |
| rs750995291 | snp | A/T | 5.81401e-05 | 0.00539135 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269238 | TTTACTGAGAAAAAA[A/T]CTTCAGAAATGTTCA | 57630 |
| rs751004686 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224677 | AACTGGCTCCAGGGG[A/C]TAACAGTAGCTGCAG | 57630 |
| rs751032168 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098144 | AATAATACATGCTTA[C/T]TATTGTTTTAAGCCA | 57630 |
| rs751037419 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101675 | GTTTAAAAAAAAGGC[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs751037470 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209385 | ATCCACTTCATCCGG[C/G]ATGCTTTCCCTGATG | 57630 |
| rs751043770 | snp | C/T | 1.80026e-05 | 0.00300016 | missense | SH3RF1 | GRCh38.p7 | 4:169136359 | CAGACAGCTCGCTGA[C/T]CCGTGCAGCAGCAGT | 57630 |
| rs751049010 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131412 | GACAGGGACTCACTA[C/T]GTCACACTTCTTATT | 57630 |
| rs751055565 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225510 | AATCATGCTGTGTGC[A/G]AGAGGGTTAAAAGCA | 57630 |
| rs751080013 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237580 | CATGCTAAAAATATG[A/C]ATTTGGGAATTATAT | 57630 |
| rs751088048 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132534 | CGCAGAAGGACAAAA[A/T]GTAGAAGTAAACCAG | 57630 |
| rs751098772 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113493 | CAAAAGATTTATGAA[C/T]ATTTAGAAAGGGAAA | 57630 |
| rs751111427 | in-del | -/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169273055 | ATTTTCTTTTCTTTT[-/C]CTTTTTTTTTTTTTT | 57630 |
| rs751119653 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177186 | TACAAAGCAAATAAG[G/T]GATGGTATGGCATCC | 57630 |
| rs751170363 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116983 | TAGTCCTTTTCCTAT[G/T]ATTCATTCCCTTTTC | 57630 |
| rs751200895 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246327 | GAGTTAACTAGAGAA[A/C]ACAAATTTTCCCCAG | 57630 |
| rs751213060 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153382 | ATTTATAAGATATAA[C/G]AGAATTATTTACCAA | 57630 |
| rs751230294 | snp | G/T | 1.70819e-05 | 0.00292244 | missense | SH3RF1 | GRCh38.p7 | 4:169116302 | TTTGGTTGCTGAACT[G/T]TTCCCACAAGCTGAT | 57630 |
| rs751242917 | snp | C/T | 6.5925e-05 | 0.00574092 | missense | SH3RF1 | GRCh38.p7 | 4:169122121 | GGGCGAGTCTGCGGC[C/T]GTAAATGTGCAATCT | 57630 |
| rs751245471 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217069 | TTGGGGAGCTGAGGT[A/G]AGAAGATCGCTTGAG | 57630 |
| rs751254255 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242988 | GTTTCTAATGCAGGT[C/G]GTCCTTGGACCAGAC | 57630 |
| rs751265733 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165544 | AAAACAAAAAACTAG[C/T]AAGGTATGGTGGCAC | 57630 |
| rs751295225 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116801 | AATCTTAGCTGGATC[C/T]CCAGACACTATCTAT | 57630 |
| rs751303377 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261494 | AAATTGGACAAGTTA[C/T]TTAAAGTCTTTCAGC | 57630 |
| rs751310865 | snp | A/G | 1.65748e-05 | 0.00287874 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122064 | GACTTCGTTTAAATG[A/G]ACACATAAGCAGTAA | 57630 |
| rs751326644 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158287 | CACAGGAATTAGTTG[C/T]CAAGGTTGGAGTGAA | 57630 |
| rs751333491 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202865 | CTTCAATAAAAGAAA[C/G]TTTAAAAAACTGGCA | 57630 |
| rs751352892 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169766 | AGGGTCTTACTCTGT[C/T]AACCAGGCTGGAATG | 57630 |
| rs751362072 | snp | A/C | 3.60516e-05 | 0.00424553 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156374 | AGAGGTAGAGCTGGC[A/C]AACAGAAAACAAGCA | 57630 |
| rs751409013 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103187 | GTGATCCACCCACCT[G/T]GGCCTCCCAAAGTGC | 57630 |
| rs751442788 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158290 | AGGAATTAGTTGTCA[A/G]GGTTGGAGTGAATGA | 57630 |
| rs751449564 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134465 | ACTCTCTTAAAGCTA[C/T]TCCCATTCTGAGCTG | 57630 |
| rs751482117 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204380 | ATCAAAACAACATAT[G/T]TTTATAATAATGTCT | 57630 |
| rs751491084 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269422 | TATTCCCTGTCTGAA[C/T]AGTGTAGCTTTGCTT | 57630 |
| rs751513353 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132322 | ATTAGCTGTTAATGA[A/C]CTCATGGTTTTGGGA | 57630 |
| rs751517215 | snp | G/T | 1.64792e-05 | 0.00287042 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169096576 | CCCATTACGTTGTAA[G/T]GTGCCTTTGAACCAG | 57630 |
| rs751535659 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147029 | AAAGAGGTACAAATA[C/G]CTATTACTTTTGGAG | 57630 |
| rs751555612 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253269 | ATTCTTCTTAATCCA[G/T]AAGGAAATGTTAGGT | 57630 |
| rs751580383 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247087 | ACTTCAAGGGGCTAT[C/T]TAGCAGAGTAAGACA | 57630 |
| rs751606458 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176074 | CAGTAAGAAGGTGGC[A/C]AGCCAGGATGAGAAC | 57630 |
| rs751606650 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190610 | AAAAAAGTCCAGTAC[C/G]AGATGGATTCACAGC | 57630 |
| rs751633279 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264438 | CTAGGAGTTAGAACT[C/T]CAACGTAGCAATGTT | 57630 |
| rs751649886 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192643 | ACTACTGGGTATCTA[C/T]CCAAAGGAAAAGAAG | 57630 |
| rs751654748 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100373 | TAAGACTGAGTTTCG[C/T]TCTTGTCACCCAGGC | 57630 |
| rs751663472 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178512 | CAGCAAAGCCAAGAC[C/T]TGGGCCCAGACCTGG | 57630 |
| rs751667338 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124773 | TGTGGGTTGCTTTAT[A/C]AACAACCTAAACCAA | 57630 |
| rs751682166 | snp | C/G | 1.67211e-05 | 0.00289142 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116518 | AGGCGCAGGTTGTGG[C/G]GAGGCCAGCGAGTGA | 57630 |
| rs751684801 | snp | C/G | 1.82131e-05 | 0.00301765 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268829 | ACTTACCCTCACTGG[C/G]GGGCTCCAGGATTGC | 57630 |
| rs751690056 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160620 | TGTGCATCTGGCTGT[A/G]TTTTTCTATGGTATT | 57630 |
| rs751691683 | in-del | -/GA | 1.65916e-05 | 0.00288019 | frameshift-variant | SH3RF1 | GRCh38.p7 | 4:169136461 | CTTGTTGGCCATAGT[-/GA]GAGGGAAGTGAAGGA | 57630 |
| rs751721486 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263256 | TTAATCCAAGGACCA[C/T]GAACTACAAAAAAGA | 57630 |
| rs751725973 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113867 | GGTATAGCATTAGAG[A/G]AAAGACACAAGGGGA | 57630 |
| rs751732407 | snp | C/G | 1.68593e-05 | 0.00290334 | missense | SH3RF1 | GRCh38.p7 | 4:169107033 | TCCACAGGGCAGGAG[C/G]CTGCCCTGCCATGGC | 57630 |
| rs751734208 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150014 | TCATTCCCTAGAAGA[A/G]GAAGCTAGCACCCCC | 57630 |
| rs751739793 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193625 | GGCTTATTGTAATGG[C/T]TGAGTAATTATTACA | 57630 |
| rs751809503 | snp | A/T | 2.11026e-05 | 0.00324821 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156685 | GAGGTATACCCTTTA[A/T]AAAAAAAAGAGGGAT | 57630 |
| rs751815072 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124338 | CATCTATGCACCTGA[-/T]TAAAAACATGTCATC | 57630 |
| rs751816193 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101146 | GCTTGAAGGATGAGA[C/T]GATGCTAAATTCACT | 57630 |
| rs751824369 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134217 | GGAATATGGAAGGAG[A/G]GGTGGAATGGTTGAA | 57630 |
| rs751914739 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231252 | GTCATGTTTGTTATC[A/C]CAAATTTGTTACTCA | 57630 |
| rs751919250 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192559 | TAAACTAGTACAACC[A/C]CTATGGAAAACAGCG | 57630 |
| rs751920582 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105355 | GAATAGTGCCTCATT[A/G]TTGAGTTTAAATAAT | 57630 |
| rs751934677 | snp | G/T | 5.07069e-05 | 0.00503497 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106942 | AACTGCGGAGTCCAG[G/T]GAACTTGCCTTCCTA | 57630 |
| rs751942495 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154301 | GTTTGAATTACTTTC[C/T]CATGGATATACAGTA | 57630 |
| rs751948820 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194386 | CCCAAAATGCAACCA[C/T]AATCATGGCTTTTGC | 57630 |
| rs751967153 | in-del | -/CTGGGGGGCTCCAGGATTGCACCCGAGGCTGCTGTCCGCCCTGGG | 5.0923e-05 | 0.00504568 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156684 | GAGGTATACCCTTTA[lengthTooLong]AAAAAAAAAGAGGGA | 57630 |
| rs751969049 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184124 | ACTGCTCTGAAGGTA[C/G]CAGACCTCAGGGCAC | 57630 |
| rs751983275 | in-del | -/TTAAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267183 | AAAATTCAAAAGACA[-/TTAAG]TTGAGTGTTTGAGCC | 57630 |
| rs752003708 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140687 | GGTTGCCCTCTTTGC[C/T]AGAGAGAATATAGCC | 57630 |
| rs752038893 | in-del | -/CTACTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175205 | CACTTCTGACAATTT[-/CTACTG]CTACCAGCCCAAGCC | 57630 |
| rs752074418 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206517 | GTCTCCATAAAAAAT[G/T]TTTAAAAATTATATA | 57630 |
| rs752091680 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126810 | TGCCCATGCTGGTCT[C/T]GAACTCCTGGCCTCA | 57630 |
| rs752108358 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250344 | AAGCTTGCGGCAAGA[C/T]TATTTTTTAAATCAT | 57630 |
| rs752110476 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190588 | CATTTTAAAATTACC[-/A]AAAAAAAAAAAAGTC | 57630 |
| rs752131047 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117617 | CTGGATGTGAGCTGC[C/T]GATACCACAGCTGCG | 57630 |
| rs752137262 | snp | C/G | 1.65732e-05 | 0.00287859 | missense | SH3RF1 | GRCh38.p7 | 4:169136464 | TGTTGGCCATAGTGA[C/G]GGAAGTGAAGGAGTG | 57630 |
| rs752144172 | snp | A/C | 0.000119673 | 0.00773449 | missense | SH3RF1 | GRCh38.p7 | 4:169136565 | CATTCTCCAGCATCA[A/C]CTCCTGGCACAGGAG | 57630 |
| rs752145338 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269677 | GGAGAAGCTGACAGA[A/G]GCCATTGAAAGTTTC | 57630 |
| rs752147049 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234807 | GGGGTTTCTCAGTCT[C/T]GGCACTACTGACATT | 57630 |
| rs752150350 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188883 | TTTTGGTGGTTGCGT[C/T]ACTAAGAAAATAGTT | 57630 |
| rs752162505 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118737 | GCTGGGATTACAGGT[G/T]TGAGCCAACGCGCCT | 57630 |
| rs752164122 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159380 | CAGCAATCGACAGAG[A/G]GAGAGAGATAGAGAG | 57630 |
| rs752177232 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221841 | GCAGGCTATGTAAAG[A/G]TCCAAAATCGTTACA | 57630 |
| rs752205627 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095969 | CCAAAGAAGAAAACC[A/G]AATTAGAGAACTGGG | 57630 |
| rs752241975 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175949 | GGATGAGGTCATGGG[A/G]TGGAGGTCCCATGAT | 57630 |
| rs752247680 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169145144 | ACTTGTACGTTTATT[A/G]CAGCACTATTCACAA | 57630 |
| rs752250699 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218659 | CACCACCATCTCAAT[C/G]TAAAATGCAGATACA | 57630 |
| rs752305747 | snp | A/G | 1.65132e-05 | 0.00287339 | missense | SH3RF1 | GRCh38.p7 | 4:169136482 | AAGTGAAGGAGTGCC[A/G]CTTTTTGGTGTTCTT | 57630 |
| rs752311669 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229117 | TACTTAAGAGTTTTG[-/T]TTTGCTTTTTGTTTT | 57630 |
| rs752321962 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115704 | CATTTCCCCGCCACC[A/C]CCCCTGGGTCCATGG | 57630 |
| rs752328783 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224270 | GTAGAGAGCTATAAA[C/G]AGAGGAAATGGCATA | 57630 |
| rs752335833 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146797 | AGGCTTTTGGGGAGC[A/G]TAAAAAGCTGATCAT | 57630 |
| rs752344843 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260288 | AAAACAAAAACAAAG[A/C]ATTTTGAGAAGACAA | 57630 |
| rs752361525 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158642 | GGCAGAGAGCTATGT[A/G]CAAAGCACAGGCCTC | 57630 |
| rs752365391 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220412 | CGGTCAAAAATGAAA[-/G]AACCGAATGAACTTC | 57630 |
| rs752384351 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162783 | CTGCAGCCAGCCAGC[C/T]CCCCTCCTTATTCCA | 57630 |
| rs752399659 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135911 | TTAAGGTAAGTTACA[C/T]AGATACAAGCAACTA | 57630 |
| rs752412107 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189160 | CATTGTGGTTCTCAC[A/T]ATTCTATTTCCGTTG | 57630 |
| rs752422055 | snp | A/G | 1.65364e-05 | 0.0028754 | missense | SH3RF1 | GRCh38.p7 | 4:169116420 | CTTGGGGAAGTCAGT[A/G]GAGCAGCTGCTGCAC | 57630 |
| rs752425469 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131303 | TGATTGAACTAAAGT[C/T]TGAAACTAAGTAGAT | 57630 |
| rs752457716 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119943 | CTTTCCTCAGTGACC[A/C]AAAGCTGAACTATCT | 57630 |
| rs752475259 | snp | A/G | 1.64833e-05 | 0.00287078 | missense | SH3RF1 | GRCh38.p7 | 4:169122130 | TGCGGCCGTAAATGT[A/G]CAATCTGGTCAGTGG | 57630 |
| rs752483474 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246196 | ACTTTGAAATCAAAT[C/T]ATTTCAGAATATTTG | 57630 |
| rs752514208 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155744 | TCATGAATTAAACGG[C/T]AGCTACCAGCCCACC | 57630 |
| rs752541700 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121463 | GAGCTACACCTGCTT[C/T]TTATGCTCAGTTCTA | 57630 |
| rs752575977 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229212 | ACTCATCTTTATAAT[A/T]CCTTTTTTATTGAGA | 57630 |
| rs752631740 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108506 | CGCTGCTCAAGGACA[C/T]GTGAACCTATGGGCT | 57630 |
| rs752652559 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201675 | TTTGTATTCATAATA[C/T]CATAATCATTTCCAT | 57630 |
| rs752655184 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219818 | TCATTAATTATTAGA[A/C]AATCAATTATTTACA | 57630 |
| rs752675983 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247461 | TGGTAACACGAGGCA[C/T]GTATGAAGGTGTGAG | 57630 |
| rs752685786 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125126 | TTTTGCCATGTCCAG[A/G]TTCTCTTCTCCTGAC | 57630 |
| rs752704374 | snp | A/G | 1.65559e-05 | 0.00287709 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122073 | TAAATGAACACATAA[A/G]CAGTAACAGACGACA | 57630 |
| rs752707708 | snp | A/C | 4.94409e-05 | 0.00497172 | missense | SH3RF1 | GRCh38.p7 | 4:169156500 | CTGAGGTAACGGTTT[A/C]ATAATCTGCACAAAG | 57630 |
| rs752709985 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262156 | AGATTTCATAGATAT[A/G]GTAAATGAATTAGCA | 57630 |
| rs752712588 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265952 | ATTTATATATATGCA[C/T]TTTAACTTCTGCAGC | 57630 |
| rs752754007 | in-del | -/A | 3.82977e-05 | 0.00437577 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269231 | ATCTACTTTACTGAG[-/A]AAAAAATCTTCAGAA | 57630 |
| rs752763208 | snp | A/G | 1.83035e-05 | 0.00302513 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116608 | CACTGCTGCCGTGGG[A/G]CGTTCCTGGTTGTGC | 57630 |
| rs752801070 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205237 | GGAAGAAAGTTAATG[C/T]CAATAAGTCTAGCTT | 57630 |
| rs752801434 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155890 | TTGTTTTAGATTGAT[C/T]CTCAGATGCTCCTCA | 57630 |
| rs752801844 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125194 | GAAGGAGCATGGCCT[C/T]TGGGGTCAAAAAAAA | 57630 |
| rs752816248 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099709 | TTAGATTAATATATG[C/T]ATTTTATAAAATGCA | 57630 |
| rs752841143 | in-del | -/TTT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103087 | CACCGCGCCTGGCTA[-/TTT]TTTTTTTTTTTTTTT | 57630 |
| rs752847546 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220691 | CTCTGTCAAACAACT[C/G]ACCCGCAAACTCTAT | 57630 |
| rs752869862 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225598 | TCTGGAGACTGTCAA[C/G]ACTGCAGTTTCATCA | 57630 |
| rs752869936 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249189 | GCCGAGATCGTCCCA[C/T]TGCACTCCAGCCTGG | 57630 |
| rs752876389 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126663 | ATCATGGTTTACTGC[A/C]GTCTCAACCTCCTGG | 57630 |
| rs752881249 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111321 | GTGCAGTGGCATTAA[C/T]ATAGCTCACTGTAGC | 57630 |
| rs752888820 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206344 | CCCACGCCCACCTAG[A/G]AGTTTGCCAGCACTG | 57630 |
| rs752893484 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191798 | AGTGGGGGAGAAAAG[-/C]CTTTTTCAACAAATG | 57630 |
| rs752904658 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159213 | GTCACATTACATTAG[C/T]GTCCAACTCTGGGGA | 57630 |
| rs752942373 | snp | A/G | 4.24737e-05 | 0.00460815 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130032 | GAAATAAAAATGGGA[A/G]AAACTATACTCACTC | 57630 |
| rs752971534 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098545 | TGGCTGCTTGAACAA[C/T]CTGAGCTCCTTTGGC | 57630 |
| rs752988823 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148324 | TGAGCAAGACATTTG[A/T]CTACAAAATGGTAAA | 57630 |
| rs753008698 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250205 | GTAGCTTTAAAAGTA[C/T]GAACACTGAAGTACA | 57630 |
| rs753034618 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128892 | AGGCCCAACTTGCAA[C/T]AGCCCTCAACCGAGC | 57630 |
| rs753044166 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152640 | TACTTGGGAGGCTGA[C/T]GCAAGAGAATTGCTT | 57630 |
| rs753061437 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241359 | AGAAGCGACTTGAAT[A/C]GATTTTCTTCAGCAA | 57630 |
| rs753065849 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182345 | AAAATCACTGAGCAG[C/T]TGCTTGTGCATGATA | 57630 |
| rs753076599 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169315 | AAAAAAATAACAAGA[A/G]ACTGGGTGCAGCAGC | 57630 |
| rs753089960 | snp | C/T | 1.69539e-05 | 0.00291147 | missense | SH3RF1 | GRCh38.p7 | 4:169107156 | GACACGCGGGGCTTC[C/T]GTTTAGTGGAGGCGC | 57630 |
| rs753120048 | snp | G/T | 0.000138117 | 0.00830899 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156698 | TAAAAAAAAAAGAGG[G/T]ATGAATTTTAATAAA | 57630 |
| rs753155605 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105120 | AAAAACATAACACTT[C/T]ATAGTAAGATTTCAA | 57630 |
| rs753163797 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139314 | GAGAAATGATCTCTG[C/T]CCTTAAGGACCTTAC | 57630 |
| rs753168402 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246835 | AAAATCCCATTCAAA[-/T]TTTTTCATCTATAAA | 57630 |
| rs753179649 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270101 | AAGCAAGCCACTTAC[C/T]GCGCCGCTCTCCCCC | 57630 |
| rs753192712 | in-del | -/TGTGTGTGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187521 | CAACGAATTTCTGTG[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 57630 |
| rs753214397 | snp | C/T | 1.68363e-05 | 0.00290136 | missense | SH3RF1 | GRCh38.p7 | 4:169107039 | GGGCAGGAGCCTGCC[C/T]TGCCATGGCCACCTC | 57630 |
| rs753271758 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120787 | AAGCTTCTCTGTTTA[A/G]AACATAGTAAACAAT | 57630 |
| rs753280716 | snp | A/G/T | 3.29578e-05 | 0.00405931 | missense, synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169120911 | ATCCTGGCAGCGCTC[A/G/T]AACACTAAAAACATC | 57630 |
| rs753285854 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240511 | GCCCCCTTCACTTAA[A/T]TATTTAAGAAAGCAG | 57630 |
| rs753293973 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245975 | CTGTTCAAATATCAA[C/T]TGCTTAAGTCAAACA | 57630 |
| rs753304738 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170095 | AAAGTCTTCCAATTC[A/G]AATATACTGATCACC | 57630 |
| rs753340482 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106600 | TGGACACAATTCAGG[C/T]GTGGCAGAGTAGAGA | 57630 |
| rs753343374 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258498 | TGCTACTATAGTACA[A/G]TTAAGACAGGAATGA | 57630 |
| rs753356028 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108477 | ACAGTGCACCATAGT[C/T]CCCAGTTACCTAACG | 57630 |
| rs753363202 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191610 | TAAGCAAAAAGAACA[A/C]ATCTGGAGGCATCAC | 57630 |
| rs753383438 | snp | C/T | 6.73117e-05 | 0.00580098 | missense | SH3RF1 | GRCh38.p7 | 4:169107045 | GAGCCTGCCCTGCCA[C/T]GGCCACCTCCTGGTG | 57630 |
| rs753383460 | snp | C/T | 1.65723e-05 | 0.00287852 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155622 | ATCATTAAGCTGTAC[C/T]ATTAAGCTTGTCATT | 57630 |
| rs753388671 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188173 | AGAATAAATTTCTGT[G/T]GTTTTAATCTACAAA | 57630 |
| rs753392390 | snp | C/T | 1.7144e-05 | 0.00292775 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155430 | CATAATTAAGATTTA[C/T]TTAGTAAGCTGAATA | 57630 |
| rs753415351 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222124 | TCAAAGCAAAGATAC[C/T]GCAATAGAAAATCAG | 57630 |
| rs753430027 | snp | A/G | 1.67086e-05 | 0.00289033 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120803 | AACATAGTAAACAAT[A/G]TATTCAAAACCATAC | 57630 |
| rs753433387 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256841 | CTCCTGGCCACAACT[A/G]ATCCTCCCACCTTGG | 57630 |
| rs753461088 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139140 | TAGCAATGAGGTCTC[A/G]TTATGATATCTAGCT | 57630 |
| rs753468477 | snp | C/T | | | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169270876 | CGCGCCTCGGCTCCT[C/T]CTCTTTGTTCGCGGC | 57630 |
| rs753486074 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143312 | TCAACATGTAATCCA[C/T]GTAAAAAAGTACTGA | 57630 |
| rs753491215 | snp | A/G | 1.79796e-05 | 0.00299825 | missense | SH3RF1 | GRCh38.p7 | 4:169136362 | ACAGCTCGCTGATCC[A/G]TGCAGCAGCAGTGGG | 57630 |
| rs753513105 | snp | A/G | 1.74233e-05 | 0.0029515 | missense | SH3RF1 | GRCh38.p7 | 4:169136590 | CAGGAGGCTTATCCC[A/G]TTCTATCAGCTGCTT | 57630 |
| rs753513982 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234642 | TTGGTAGAAAGTACT[C/G]CCTGGCATTGTTTGG | 57630 |
| rs753517003 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231211 | CCCATTATTACATTA[C/T]TGTTGTTCTTACTAT | 57630 |
| rs753550131 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149313 | GGAGCTCAGAGGAGA[C/T]CTGCTTTTGCCTTTA | 57630 |
| rs753603547 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133176 | TCCCTAATAACTTTG[C/T]GGTGCTATTATGCCA | 57630 |
| rs753626706 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226160 | CTTTTGTTTAGTGCA[C/T]TTAATATGAATGAAA | 57630 |
| rs753637029 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100239 | CTCTCCCATGACCTA[C/T]ATGGGACCTGCTGAT | 57630 |
| rs753702623 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125007 | ACAGGCAAAAAACAG[-/C]TATGGACCTTCTAGA | 57630 |
| rs753785828 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153490 | CTAGAGAAAGACCAT[-/TA]CTTAAGAAAAAGCCC | 57630 |
| rs753788925 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214119 | TGGAGGTGGGGCCTC[C/G]AGGGAAGTGTTTGGG | 57630 |
| rs753832346 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137735 | ATGGAAACTCTCTCA[C/G]TCAATATTTTATGAA | 57630 |
| rs753841644 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113103 | AGGCATGTGCAAGTC[C/T]CAGTTTTCTTTTTTT | 57630 |
| rs753848980 | snp | A/G/T | 3.30963e-05 | 0.00406783 | missense | SH3RF1 | GRCh38.p7 | 4:169116438 | GCAGCTGCTGCACAG[A/G/T]CCAGAGGGGCACTGG | 57630 |
| rs753850201 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166814 | CTGGTCCTCAATTGA[A/G]TTCCTCTAGAAGAAC | 57630 |
| rs753853745 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229704 | GAGTATTACTCATGA[A/G]TAAGCCCCACAGCTT | 57630 |
| rs753865915 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103847 | ACTTGGGTAGAAATC[C/T]TCTCCAAAGACCCCT | 57630 |
| rs753896329 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215523 | TGTAGAGAGTTGGTA[C/T]AATTTCTTCCTTCAG | 57630 |
| rs753900998 | snp | A/G | 1.88014e-05 | 0.003066 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106835 | TTTTTCCTGGAACGA[A/G]GTTGAACTTACCTTT | 57630 |
| rs753943490 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199599 | ATGGTCCTGGAAAAT[-/G]TGGCTTAGTGAATGC | 57630 |
| rs753950204 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217320 | GTGGGAAGAGCGGAC[C/G]GACCTGGGAAGAAAT | 57630 |
| rs753954824 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182568 | GAGACATTTTATTAG[C/T]CTCTATCACAGACTA | 57630 |
| rs753958455 | snp | A/G | 6.59174e-05 | 0.00574059 | missense | SH3RF1 | GRCh38.p7 | 4:169117567 | ACTGTCATTTGCCCC[A/G]TCATGTGCAACAAGA | 57630 |
| rs753959802 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252839 | TAAATAAATCCTAAA[C/T]TGGCAACAACCCACA | 57630 |
| rs754010593 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139036 | TGCTCAGTGCAGCCT[C/T]GAACTCCTGGGCTCA | 57630 |
| rs754017183 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201832 | TGGGGATGAGGTCTT[A/G]ACACAGAAAACCCAT | 57630 |
| rs754020186 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | SH3RF1 | GRCh38.p7 | 4:169096601 | AACCAGCCATCCTCT[C/T]GTTTTTTATGAACAA | 57630 |
| rs754027592 | snp | C/G | 1.81105e-05 | 0.00300914 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136304 | TTTTATATAACACTT[C/G]TTTGAGGATTTACCT | 57630 |
| rs754041179 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169868 | GAATAGCTCGGTCCA[C/T]TGGAAATGAGGCTTT | 57630 |
| rs754098194 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158374 | CCTGGAGGTAAGAAG[G/T]CACATGTGCAGCGGG | 57630 |
| rs754121883 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124894 | AGAGTAAAACCACAC[A/G]TAGCCTTTCATTCAC | 57630 |
| rs754157069 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267383 | TAAGCTAAACAGACC[C/T]ACATCAGGTGTCTCA | 57630 |
| rs754185499 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208101 | TAAAATAAAAGCATA[C/T]GTGGAAACGTAAAGA | 57630 |
| rs754193931 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175774 | TATATCCATACCTGA[C/G]GCAAGTTGTACACAC | 57630 |
| rs754211042 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130377 | TGATGTGATAAATAC[C/T]GGTCACAACAGTGTC | 57630 |
| rs754221111 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242873 | AGCCTCCAGAACCAT[A/G]AGCCAAATACATTTC | 57630 |
| rs754227287 | snp | A/C | 0.00296369 | 0.0383805 | missense | SH3RF1 | GRCh38.p7 | 4:169130155 | GTGGTACTTATATGA[A/C]CCTGCCGAGAAAAGA | 57630 |
| rs754244907 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216144 | TGATATATGTTAGCT[A/G]TATTTGTATCAGTAG | 57630 |
| rs754262727 | in-del | -/T | 1.65425e-05 | 0.00287593 | frameshift-variant | SH3RF1 | GRCh38.p7 | 4:169107195 | AACTTCAACAAACCC[-/T]TTTTTTCTTTCTGGA | 57630 |
| rs754273299 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209664 | TTAACTCACACTGTG[A/G]CATAAATATACTCAA | 57630 |
| rs754280533 | snp | C/G | 1.64808e-05 | 0.00287057 | missense | SH3RF1 | GRCh38.p7 | 4:169268985 | CCAAGGCCTCTGTTT[C/G]ATGCCATCCAGAAGT | 57630 |
| rs754313701 | snp | A/T | 1.72172e-05 | 0.00293399 | missense | SH3RF1 | GRCh38.p7 | 4:169107175 | TAGTGGAGGCGCCAG[A/T]AAGCAACTTCAACAA | 57630 |
| rs754338198 | snp | C/T | 3.39121e-05 | 0.00411763 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268874 | TCCGCCCTGGGAGCT[C/T]TGCAGATCTTTTGAG | 57630 |
| rs754345108 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189431 | TTTCTTACTCCTCAT[C/T]ACAGCTCTGGAGGTG | 57630 |
| rs754362949 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181608 | GTTAATAAAATCTTT[C/T]AGGTCCCCAAAATCT | 57630 |
| rs754363447 | in-del | -/ATA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232875 | CTAAACTCTGAACAT[-/ATA]ATAATCTACTAGTCT | 57630 |
| rs754396186 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218899 | TTAGGAGTCAATGAT[A/T]CATTCAAGGTACCTT | 57630 |
| rs754447387 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182927 | AAGTTGAAGACTTCC[C/G]AAAACTACTAAAGGA | 57630 |
| rs754461916 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233624 | TGTGGTTGTCTTAGA[C/T]GGCTTTGGTTGTTTG | 57630 |
| rs754466255 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201552 | TTTAGACTTCATGTT[A/G]CTAAGTGTGTTCATC | 57630 |
| rs754469865 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108487 | ATAGTCCCCAGTTAC[C/T]TAACGCTGCTCAAGG | 57630 |
| rs754513389 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116812 | GATCCCCAGACACTA[C/T]CTATTGTCCTTCCAG | 57630 |
| rs754531424 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212722 | ATCAACCTAAGTCCA[C/T]AGTTTATATCAGGGT | 57630 |
| rs754543055 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143354 | TCTTTTTTTGTACTA[C/T]GTCTTTGAAACCCGG | 57630 |
| rs754547078 | snp | C/T | 1.79939e-05 | 0.00299943 | missense | SH3RF1 | GRCh38.p7 | 4:169136361 | GACAGCTCGCTGATC[C/T]GTGCAGCAGCAGTGG | 57630 |
| rs754558525 | in-del | -/AAAAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208986 | AAAAACACACCAAAC[-/AAAAT]AAAAAATGAGGCAGT | 57630 |
| rs754580296 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222186 | ATAAATCAATAGGCT[G/T]GTCATGGTGGCTTAC | 57630 |
| rs754581365 | snp | A/C/T | 5.9977e-05 | 0.0054759 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269254 | CTTCAGAAATGTTCA[A/C/T]AGTTGTGTGCATCCC | 57630 |
| rs754594544 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095803 | CATTCTAGGAAAATT[A/G]AAAACCCACACAATT | 57630 |
| rs754597124 | snp | C/T | 1.65337e-05 | 0.00287517 | missense | SH3RF1 | GRCh38.p7 | 4:169116406 | AAGCACTGGTGATGC[C/T]TGGGGAAGTCAGTGG | 57630 |
| rs754600254 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113505 | GAACATTTAGAAAGG[C/G]AAATAAAACTCTTCC | 57630 |
| rs754605468 | snp | C/T | | | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156437 | ATCTTTGTCTGCTTC[C/T]TTGTCTTTCACTTCA | 57630 |
| rs754630380 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130427 | GCCATTGGCTTTCAC[A/G]GTAACACATTGCCTC | 57630 |
| rs754666361 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256904 | CAATCCACTTGCCCC[A/G]GAGTTTATTTTACAA | 57630 |
| rs754700845 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114163 | TTTGTGGTAAAAATC[A/G]GGTCCTAAAATCAAG | 57630 |
| rs754709059 | snp | C/T | 1.65138e-05 | 0.00287343 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169269102 | ACCTACGATCCCCAG[C/T]AAACATCGCTTGCAA | 57630 |
| rs754712622 | in-del | -/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271629 | GAGTCGGAGCGAAGT[-/G]TTGCCCCTTAGGGCC | 57630 |
| rs754722091 | snp | C/T | 1.70635e-05 | 0.00292087 | missense | SH3RF1 | GRCh38.p7 | 4:169116303 | TTGGTTGCTGAACTG[C/T]TCCCACAAGCTGATG | 57630 |
| rs754769114 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134132 | AGGCAGCACTTCAAA[C/G]ACCTCCCAGCCTCTT | 57630 |
| rs754776973 | snp | C/T | 1.89827e-05 | 0.00308075 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107220 | TCTGGAAAAAAAAAA[C/T]AATGAGCCTTAGTTG | 57630 |
| rs754778165 | snp | A/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199764 | AATAAAAGAGAAAGC[A/G/T]AAATGGATAAAAAGG | 57630 |
| rs754783174 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118227 | TACATGCATGCACAC[A/C]CATACACGCACTAGT | 57630 |
| rs754784518 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212839 | TGTTCAAAAAAATCC[C/T]GCGTGCTCAACTTAC | 57630 |
| rs754807882 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132003 | CCTGAGAAGACTCGG[-/T]TATCCAGGGCCCTTG | 57630 |
| rs754811365 | snp | C/T | 8.28301e-05 | 0.00643492 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122070 | GTTTAAATGAACACA[C/T]AAGCAGTAACAGACG | 57630 |
| rs754832008 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165734 | AGAGAGGATGCTCAT[A/G]TAATTTAAACATAAG | 57630 |
| rs754833230 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226371 | TGCTTTTCATCACAG[C/T]TGTCGTGTCTACATA | 57630 |
| rs754838573 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158465 | TAGGCAGAGGCCAGT[C/T]TATTGAGGGTCTTGT | 57630 |
| rs754874150 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265618 | AGCTGGGGTTATAGG[C/T]ACGTGCCACCACACC | 57630 |
| rs754912362 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106640 | AAAAGGAAGGCTGGG[C/G]ACCAACCCATTAAGA | 57630 |
| rs754914503 | snp | A/G | 3.2994e-05 | 0.00406152 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169155537 | CATTCCTTCAGCCCA[A/G]TTTTCATCCACTCTT | 57630 |
| rs754930954 | snp | A/T | 1.80231e-05 | 0.00300187 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156376 | AGGTAGAGCTGGCAA[A/T]CAGAAAACAAGCACA | 57630 |
| rs754945352 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103350 | TCCCAATAATATAAA[C/T]TGAAAAATACTTCTG | 57630 |
| rs754952019 | snp | C/T | 0.000492984 | 0.0156923 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116258 | GAAACAGTAAGTAAG[C/T]ATGGTCTTACTTTGC | 57630 |
| rs755025255 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168944 | ATGAGAATATGAATT[C/T]GCCTACAGAAATCAA | 57630 |
| rs755041590 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260620 | CTCTTTCCTCCCTTT[A/C]CCTCGGATTTTCCTT | 57630 |
| rs755048935 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182636 | CTTATAAAAGGCTTA[C/T]GGGAAATATGGCTGG | 57630 |
| rs755053097 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153405 | TTTACCAATTTTTGT[C/G]ATGCAGCCTGTTTTT | 57630 |
| rs755054370 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247089 | TTCAAGGGGCTATTT[A/G]GCAGAGTAAGACATG | 57630 |
| rs755100228 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247706 | GCATCATGACATTCC[C/T]GCACACGACAGAAAC | 57630 |
| rs755120909 | in-del | -/AC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186829 | GCTAACACGGTGAAA[-/AC]CCCCATCTCTACTAA | 57630 |
| rs755132464 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158379 | AGGTAAGAAGTCACA[C/T]GTGCAGCGGGACTGG | 57630 |
| rs755150869 | in-del | -/G | 0.000120493 | 0.00776094 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156696 | TTTAAAAAAAAAAGA[-/G]GGATGAATTTTAATA | 57630 |
| rs755162958 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189521 | GTACACTGTTGCTTT[C/G]CTCTCCCCAGGACTC | 57630 |
| rs755190122 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248526 | GAACATTAGGACAAA[C/T]ACCTAATGCACGCCA | 57630 |
| rs755193379 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204784 | TCGATCTCCTGACCT[C/T]GTGATCCACCCGCCT | 57630 |
| rs755212437 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110170 | GCTTGAGCCCAGGAG[C/T]TGAGAGCAGCCTGGG | 57630 |
| rs755212853 | snp | A/G | 1.88898e-05 | 0.0030732 | missense | SH3RF1 | GRCh38.p7 | 4:169122203 | CGGCGGTGGCGCCTG[A/G]TGGTGTGGAGGCAAG | 57630 |
| rs755231968 | snp | A/G | 1.71599e-05 | 0.0029291 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156692 | ACCCTTTAAAAAAAA[A/G]AGAGGGATGAATTTT | 57630 |
| rs755233348 | in-del | -/CTCAACATATGAAATTGGAAATATTCCTATTTTGT | 5.37216e-05 | 0.00518246 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169136620 | AGCAGCCGAGTTAAA[lengthTooLong]CTGCAAAAGCAACCA | 57630 |
| rs755268716 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161907 | CTTTTGGGTCAGGCA[C/T]GGTAGCTCACACCTG | 57630 |
| rs755280028 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236142 | TCCTGGCTCTACCAT[A/G]AACATTACGATTCTT | 57630 |
| rs755281682 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240440 | TGGGCTCAAGCAATC[A/G]ACCTACCTCAGCCTC | 57630 |
| rs755302406 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111269 | TCACACCACTGCACT[C/T]CAACCTGGGTGATCT | 57630 |
| rs755354633 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162623 | AAAACTACCAGCACT[C/T]TGAGGATGGCAGCTG | 57630 |
| rs755357084 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194428 | TCCTTAGACACTCTG[A/G]TTTTGTTTTGCCTTT | 57630 |
| rs755358542 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | SH3RF1 | GRCh38.p7 | 4:169156550 | GGATTCCATTGACTT[C/T]CCCATGGTACCAATT | 57630 |
| rs755361208 | snp | C/G | 1.68858e-05 | 0.00290561 | missense | SH3RF1 | GRCh38.p7 | 4:169106950 | AGTCCAGGGAACTTG[C/G]CTTCCTATGAAAAGC | 57630 |
| rs755400659 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266965 | GTTATAAGGCTCAAG[A/T]TTAGTTGAGTTTCTT | 57630 |
| rs755407619 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228750 | TGCAGCATGGAATCA[C/T]CCATCAGTACACTTT | 57630 |
| rs755420298 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136146 | ACTCAAGTTAGCTTT[C/T]CCTTCTCCATTTTTC | 57630 |
| rs755431733 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163599 | TGTCCACATCACCTA[C/T]GTCTTTACAATCTGG | 57630 |
| rs755492985 | snp | A/C | 1.78474e-05 | 0.0029872 | missense | SH3RF1 | GRCh38.p7 | 4:169106869 | AAACGACAGGTCTAG[A/C]CTCATTCAAGACAGG | 57630 |
| rs755524119 | snp | C/G/T | 4.98909e-05 | 0.00499434 | synonymous-codon, missense | SH3RF1 | GRCh38.p7 | 4:169117731 | CACTCCCCGACTTGT[C/G/T]TGGCCAGCTGTAGAC | 57630 |
| rs755531043 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229709 | TTACTCATGAGTAAG[A/C]CCCACAGCTTACTCA | 57630 |
| rs755540623 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181770 | TCCTTTACTCCTTTG[A/G]AACTCTTCTAAGATT | 57630 |
| rs755567282 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142171 | ATACTGGTCAGGCTG[A/G]CCTCAAACTCCTGAC | 57630 |
| rs755568107 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105613 | AGAAGAGAGTTCTTC[G/T]CTAGACATCGTGGCT | 57630 |
| rs755583147 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199335 | AACACATCATTCTCA[C/T]AACAGTCTAATGTTT | 57630 |
| rs755603909 | snp | A/C | 1.67871e-05 | 0.00289711 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120797 | GTTTAGAACATAGTA[A/C]ACAATGTATTCAAAA | 57630 |
| rs755619251 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153563 | GCCCTGTAAGACAAT[C/T]GACATTACTGAAATA | 57630 |
| rs755632599 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244719 | AATTTTTTTAAATTG[C/T]GCATGTGTTACCAAA | 57630 |
| rs755635487 | snp | A/G | 1.68798e-05 | 0.0029051 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106960 | ACTTGCCTTCCTATG[A/G]AAAGCATCCTGGGCC | 57630 |
| rs755655156 | snp | C/T | 1.73902e-05 | 0.0029487 | missense | SH3RF1 | GRCh38.p7 | 4:169136586 | GGCACAGGAGGCTTA[C/T]CCCATTCTATCAGCT | 57630 |
| rs755673103 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184364 | ATCTCAGCTTCCACA[C/T]TTGAAGATTCTAGAA | 57630 |
| rs755674922 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255208 | CTTACCCAAAACAGT[A/T]CATGAATATTTTAGC | 57630 |
| rs755681415 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252885 | GGTGGATTATAGCAA[A/T]GGGGAAGTTAAACAA | 57630 |
| rs755707339 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154417 | TTTTAGTTTTCAAGA[C/T]CATGCCAAAACAAAT | 57630 |
| rs755708869 | snp | A/G | 1.65075e-05 | 0.00287289 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136492 | GTGCCGCTTTTTGGT[A/G]TTCTTCTTGGTGTCG | 57630 |
| rs755712128 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186049 | ATGTGATGGGGACTG[C/G]AGTCATTTTATTTGA | 57630 |
| rs755722459 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232587 | AAAGTACAAACTTTG[A/G]TCACATCCTATCCCA | 57630 |
| rs755741224 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233393 | TTACCAAATTTCAAA[C/G]AATTAGAATAAAATA | 57630 |
| rs755747376 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161143 | GGATGCTTAAAAGGA[C/G]AGAAAGCCAAAGAGA | 57630 |
| rs755769743 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141116 | TGGTATAGAACATTA[C/T]GAAGTAAAAAGTAAA | 57630 |
| rs755770285 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257981 | AAATGTGAGAGCCAC[-/AT]GTCACCTCAATGCAC | 57630 |
| rs755821135 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264612 | CCTACCTTTCTTTCC[C/T]GATCTCTCCATTCTT | 57630 |
| rs755850877 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221006 | CATGGTCTTTGAACT[C/T]TCGTGTCGAAAGAGT | 57630 |
| rs755864445 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126993 | TTGCAGTTAACCACC[C/T]CTTGGCTGGTCCAGA | 57630 |
| rs755880059 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105877 | CGCAACAGAGCAAGA[A/C]CCTGTCTCAAAAAAA | 57630 |
| rs755901442 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205999 | CAAAAACAATATATT[C/G]ATATTTTTAACTGAT | 57630 |
| rs755908461 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131584 | TAGGGTCTGAAGGCA[A/G]GGAACCTAAGGCTGT | 57630 |
| rs755910339 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148295 | CTTTCTCGATTCCTG[G/T]CTCTGTGTCCCCCTG | 57630 |
| rs755929767 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225788 | GTGTCTTAAAAGTAA[A/C]AATAGTTAACTTGCA | 57630 |
| rs755936759 | in-del | -/AAGATA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173286 | TGACCATTCCTGATT[-/AAGATA]TTCAGTTGCACCAAA | 57630 |
| rs755943321 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134925 | TGTCTTTATTTCTCA[A/G]TAAGAGTTTCATGGC | 57630 |
| rs755948040 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231200 | CACAAATGTGGCCCA[C/T]TATTACATTATTGTT | 57630 |
| rs755974319 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119629 | AATGTAGATTTTAAC[-/AT]ACATAGAAAAGAATG | 57630 |
| rs755982660 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263346 | CTGCTGCCTTACTTG[C/T]TGTTTCTTGTGTGTT | 57630 |
| rs755989325 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179066 | TGAATCTGTTGCCTT[A/C]CATGGCAAAAGGGAT | 57630 |
| rs755998313 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133100 | TCTCTAATTGCCATA[C/T]AGAAACCAGGGCATA | 57630 |
| rs756015050 | in-del | -/T | 1.7978e-05 | 0.00299811 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136627 | GAGTTAAACTGCAAA[-/T]AGCAACCAACAAACC | 57630 |
| rs756017942 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212783 | GAAAAATGTTTAATC[A/G]CATGTATCCACCATT | 57630 |
| rs756088499 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | SH3RF1 | GRCh38.p7 | 4:169096581 | TACGTTGTAATGTGC[C/T]TTTGAACCAGCCATC | 57630 |
| rs756100373 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194413 | TTGCCTAAGTATGCA[A/T]CCTTAGACACTCTGG | 57630 |
| rs756126507 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097510 | TATTATCTGTGCCCC[-/T]GCCTCCATGCTCCTT | 57630 |
| rs756149549 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195064 | GATAATTTTTATCCT[G/T]CCTAAATAACATACT | 57630 |
| rs756169308 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272977 | AGAGAGCAGCACACA[A/G]GGTCATAGATAGAAT | 57630 |
| rs756192032 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181551 | CAGGCGTGAGCCACC[A/G]CGCCAGCCCTGGGAA | 57630 |
| rs756231309 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167215 | AGATGTTTGTATAGC[A/C]ATGGAAGGGCACTCA | 57630 |
| rs756254159 | snp | G/T | 1.65701e-05 | 0.00287833 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117490 | CAGGTAAGCCCTTTA[G/T]CCTGATATGTTCTGG | 57630 |
| rs756266588 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135982 | TGGAGATAAAGTTTT[A/G]GTTGGCAAGATCTCC | 57630 |
| rs756279594 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251507 | TGTCCTTAAACAGGC[C/T]ATCCGAAAAACAGAA | 57630 |
| rs756299914 | in-del | -/AAGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177463 | AAAGAGCTATTATAA[-/AAGT]AAGCATTGAAATTAT | 57630 |
| rs756300465 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250635 | ATACAGACAGGAATA[A/T]ATTTAATCAAAGTCC | 57630 |
| rs756308950 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166457 | TCCTCATCTGCTATA[A/T]ATTCCAGAAGTGCCA | 57630 |
| rs756335061 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108688 | CCTCAGCTGATCTTA[C/T]GCGCTTTCGCTTCAC | 57630 |
| rs756340632 | snp | C/T | 1.83273e-05 | 0.00302709 | missense | SH3RF1 | GRCh38.p7 | 4:169116609 | ACTGCTGCCGTGGGG[C/T]GTTCCTGGTTGTGCG | 57630 |
| rs756345077 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270179 | AAAAGATTTGGCTGG[A/G]AGCATTAACAGCTGT | 57630 |
| rs756391887 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099941 | GAGTAATAGACTCTA[C/T]TTAGAAATCTTCCAG | 57630 |
| rs756424942 | in-del | -/AAAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185435 | TGCCCAGAAAAAACA[-/AAAC]AAACAAACAAACAAA | 57630 |
| rs756435650 | snp | C/T | 1.90721e-05 | 0.00308799 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130041 | ATGGGAGAAACTATA[C/T]TCACTCCAAGGGCAG | 57630 |
| rs756486935 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113311 | AGACAGGGTTTCACT[A/G]TGTTGGCCAGGCTGG | 57630 |
| rs756487008 | snp | C/G | 2.01786e-05 | 0.0031763 | missense | SH3RF1 | GRCh38.p7 | 4:169122215 | CTGGTGGTGTGGAGG[C/G]AAGGACAGTGGCAGC | 57630 |
| rs756515942 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206760 | CATAAGAAAATGACA[C/T]GTAGCGTTGCATTCA | 57630 |
| rs756550540 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238443 | AATTTACCATTACCA[C/T]GAATCTACAGGATGC | 57630 |
| rs756567971 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143295 | TCTACACTATGATCA[C/T]TTCAACATGTAATCC | 57630 |
| rs756578751 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113983 | AAGGTTGAGTTGAGT[C/T]ACAGCTGTCTGAAGA | 57630 |
| rs756601952 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260338 | GAAGGCAATGGAGAA[A/G]GACTGCTTTCCTGCT | 57630 |
| rs756611438 | snp | A/C | 1.73848e-05 | 0.00294824 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156703 | AAAAAAGAGGGATGA[A/C]TTTTAATAAAATAAT | 57630 |
| rs756640130 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227721 | AACAACTTACAGGTA[A/G]AAAGACCACATTATC | 57630 |
| rs756651884 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193850 | CTGTTAACTTCAAAA[G/T]CTGAACAAAAGGGAC | 57630 |
| rs756657149 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150204 | ATGTGTAGTTTATTG[C/T]ATGTAACTTACGTCA | 57630 |
| rs756663761 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162682 | TGTTTCTTCATTCAC[A/T]TGTCTTCTTTTTGCC | 57630 |
| rs756664934 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101424 | TCACTTACGGGGAGA[C/G]AAAGTAGAAGGGTGG | 57630 |
| rs756680232 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253411 | AGAGAATCCAGCCTT[A/G]CAGCTTTCTGAGCTA | 57630 |
| rs756692046 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259054 | AAGCATCCTATAGCT[A/C]ACTTTAGCTTTCTTT | 57630 |
| rs756715838 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269444 | GCTTTGCTTTGGAAT[A/G]TGGGTTCCTAAACTC | 57630 |
| rs756717729 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211250 | CACTTTGGGAGGCCA[A/G]GGCGGGCAGATCATG | 57630 |
| rs756725142 | snp | C/T | 1.68267e-05 | 0.00290053 | missense | SH3RF1 | GRCh38.p7 | 4:169107067 | CTCCTGGTGGCAGTT[C/T]GGGCCCCACCGCTCC | 57630 |
| rs756740962 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134500 | TATTCTTGGCAGAAG[C/T]TTGTCTTTTATTTCA | 57630 |
| rs756809387 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267857 | AAATATTCTCATCTA[A/G]ATTAATTGTTCTTTA | 57630 |
| rs756816596 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241760 | GACCTTGCAGCATGG[A/T]TACTGAGATACTGCA | 57630 |
| rs756833218 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206489 | ACCAGCCTATGCAAC[A/C]TGGTGAGACTCCGTC | 57630 |
| rs756838951 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117045 | TGATAGAGTTCACAA[A/G]CCTTTAGTTTACCCC | 57630 |
| rs756857213 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161685 | AAAGAAAATCTAGAA[G/T]ACACTCTTGTAGTGG | 57630 |
| rs756869470 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243243 | CTCACTTGCTCTAAG[A/G]TATAATTTAAAATTA | 57630 |
| rs756907710 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199001 | ATACTTTAAGGACAA[C/T]ACTTCTAGAAAGCAG | 57630 |
| rs756914133 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153397 | GAGAATTATTTACCA[A/C]TTTTTGTGATGCAGC | 57630 |
| rs756918606 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153544 | TTTACCACAGCTAAG[-/C]AATGCCCTGTAAGAC | 57630 |
| rs756926930 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104319 | AGGGAGGGAGGCTTT[G/T]TGACCAAGAGAAAGC | 57630 |
| rs756928614 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182999 | CCCGGCTGAGCAACA[C/T]AGCAGGGCAGGGAGT | 57630 |
| rs756942164 | snp | C/T | 1.78064e-05 | 0.00298377 | missense | SH3RF1 | GRCh38.p7 | 4:169136611 | TCAGCTGCTTAGCAG[C/T]CGAGTTAAACTGCAA | 57630 |
| rs757036671 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202941 | TAAAGGAAGAAGACA[C/T]AGCATTCTGTATCTA | 57630 |
| rs757057648 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234848 | AGTTGTTTGTTGGGG[A/T]GCGTGGCTGTCCTGT | 57630 |
| rs757058937 | snp | A/G | 1.65146e-05 | 0.0028735 | missense | SH3RF1 | GRCh38.p7 | 4:169136509 | TCTTCTTGGTGTCGG[A/G]GTGCTTTGGGGCAGT | 57630 |
| rs757063967 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109876 | TAGCCAGGTGTGGTG[A/G]TGCATGCCTGTGGTC | 57630 |
| rs757079566 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188682 | TCAAAATCTTTAAAG[C/T]TTTCTGGCTTATGTA | 57630 |
| rs757100123 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248407 | AAACCAAACACTGCA[A/T]GTTCTCACTCATAAG | 57630 |
| rs757119495 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147163 | ATGAAGTTTTATATA[C/T]ATGTTTCCATTACAT | 57630 |
| rs757129450 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209244 | CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA | 57630 |
| rs757169604 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189216 | TAAGCAAACACAATA[A/C]CATTTCCCAAAACAC | 57630 |
| rs757181950 | in-del | -/TTTTTTTTTTTT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119287 | TTTTTGTATTTTTTT[-/TTTTTTTTTTTT]TTTTTTTAGTAGAGA | 57630 |
| rs757216117 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212586 | CAGCAAAACTGAGCA[-/G]GAAGTACAGAGAGTT | 57630 |
| rs757264507 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238237 | AAGCTTGGTCAGAAT[A/T]AGGGTGTACCTACAC | 57630 |
| rs757268648 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113895 | GGACACACCTGCAAA[C/T]ACCTCAGGGCACCAT | 57630 |
| rs757342785 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160669 | ATGAGGCTAGAAAGC[C/T]AGTTTGGGTCAAGTT | 57630 |
| rs757343751 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100386 | CGCTCTTGTCACCCA[A/G]GCTAGAGTGCAATGG | 57630 |
| rs757348312 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227463 | GGACTACAAAAATAT[A/G]TAGTTGTCTTAACAG | 57630 |
| rs757351460 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101274 | TTAAAATGTACAAAG[C/G]TCCTTAAAAAGGAAT | 57630 |
| rs757366791 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179546 | TACCAGACATAGTAA[C/T]CAATACCAGCAACAG | 57630 |
| rs757373400 | snp | C/G | 1.65307e-05 | 0.0028749 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122082 | ACATAAGCAGTAACA[C/G]ACGACACGCTCACTT | 57630 |
| rs757375588 | snp | G/T | 1.64792e-05 | 0.00287042 | missense | SH3RF1 | GRCh38.p7 | 4:169156505 | GTAACGGTTTAATAA[G/T]CTGCACAAAGTTGGT | 57630 |
| rs757385665 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102601 | ATTTTCTTTCCACTT[C/T]CTCTTTGCAATTTCC | 57630 |
| rs757394742 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134261 | ATGGAACACAGAAAG[A/G]GCCTTGTTTCCTAAG | 57630 |
| rs757395563 | snp | A/T | 1.877e-05 | 0.00306344 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106837 | TTTCCTGGAACGAAG[A/T]TGAACTTACCTTTCA | 57630 |
| rs757401469 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259161 | TGAATTGATAAGCAG[-/T]TTTTTCTGGCAAAAA | 57630 |
| rs757409949 | in-del | -/TGTGTGTGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187545 | GTGTGTGTGTGTGTG[-/TGTGTGTGT]GTGTGTGTGTGTGTA | 57630 |
| rs757441114 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150019 | CCCTAGAAGAGGAAG[A/C]TAGCACCCCCACCTT | 57630 |
| rs757448855 | snp | A/G | 1.64781e-05 | 0.00287033 | stop-gained | SH3RF1 | GRCh38.p7 | 4:169096602 | ACCAGCCATCCTCTC[A/G]TTTTTTATGAACAAA | 57630 |
| rs757473283 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263257 | TAATCCAAGGACCAC[A/G]AACTACAAAAAAGAA | 57630 |
| rs757488315 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119996 | TGCATATCTAAAGCT[C/T]CTGTCACTCTATAAC | 57630 |
| rs757517094 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184336 | CACATCACACGTGCA[C/T]ACATCCAAATAGATC | 57630 |
| rs757542369 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119570 | TATCATTATTTTGCA[C/G]CAGGGAGGTTCTATC | 57630 |
| rs757577796 | snp | A/G | 3.30956e-05 | 0.00406776 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117497 | GCCCTTTATCCTGAT[A/G]TGTTCTGGCCTGGGT | 57630 |
| rs757579253 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243066 | GTCCAGTCTTCAAAC[C/T]CCTTCTCCCAAATCC | 57630 |
| rs757605547 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171765 | TTCCCCTCACAAAAA[A/C]CCACAGAAGACTCCT | 57630 |
| rs757620946 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140801 | GAAGCTTTACAGATG[A/T]ATCAGTCTGTAGCTT | 57630 |
| rs757622132 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205619 | AAGTGTTGACAAATA[C/T]GCACCTGTCAGAAAA | 57630 |
| rs757623047 | snp | A/G | 3.68698e-05 | 0.00429343 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116617 | CGTGGGGCGTTCCTG[A/G]TTGTGCGCTGCAACT | 57630 |
| rs757652069 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219266 | AACCCTAAATCATCA[A/G]GAGAGGGTTAATTTA | 57630 |
| rs757666265 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219970 | CCAGGCGATCAGTAC[A/C]AACTAGCGTGTGGTA | 57630 |
| rs757705352 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216460 | ATTTTCCATAACTGT[C/T]CTTGCTCCTTTTATT | 57630 |
| rs757743924 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272883 | TCCCAAGGGAAAGAA[A/G]AAACTGTTAATCATG | 57630 |
| rs757756239 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220889 | TCATTGAAGAGGTCA[G/T]GATTTTTGTTAAAAT | 57630 |
| rs757771436 | snp | C/T | 3.42683e-05 | 0.0041392 | missense | SH3RF1 | GRCh38.p7 | 4:169130071 | GCTTGGTAGGGAACA[C/T]CTGATGGGAAAGTAA | 57630 |
| rs757773567 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172630 | AGGGGTCAACTATTA[C/T]GGTTCACATTAGGTG | 57630 |
| rs757787622 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174983 | GTGTCCAAAACAGAC[C/G]TCTTGGTTTCCACCT | 57630 |
| rs757824921 | snp | C/T | 1.69352e-05 | 0.00290987 | missense | SH3RF1 | GRCh38.p7 | 4:169268875 | CCGCCCTGGGAGCTC[C/T]GCAGATCTTTTGAGC | 57630 |
| rs757829952 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159401 | AGATAGAGAGAGAGA[A/G]AGAGAGAGAACTGGC | 57630 |
| rs757836145 | snp | C/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271190 | GCCGCGCCGGCCTCC[C/G]GCGCTGAGGTGACCT | 57630 |
| rs757848227 | in-del | -/TTTTGCTATCCTTG | 1.83714e-05 | 0.00303073 | frameshift-variant | SH3RF1 | GRCh38.p7 | 4:169107204 | AACCCTTTTTTTCTT[-/TTTTGCTATCCTTG]TCTGGAAAAAAAAAA | 57630 |
| rs757895054 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097452 | GAGTTAGTGGGAAAG[C/G]TGTCATTATCGCTTA | 57630 |
| rs757904703 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209956 | ACCACACCCAGTTAA[-/T]TTTTTGTATTTGTGT | 57630 |
| rs757908384 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110512 | GTGTGAACCTGTAGT[C/T]CCAGGTGCTTGGGAG | 57630 |
| rs757955554 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176030 | CTTTCTGTCCACATG[A/C]ACATACCAAGGAAAG | 57630 |
| rs757958469 | snp | A/G | | | missense | SH3RF1 | GRCh38.p7 | 4:169106859 | TACCTTTCACAAACG[A/G]CAGGTCTAGACTCAT | 57630 |
| rs757966359 | snp | C/T | 3.54233e-05 | 0.00420837 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116278 | TCTTACTTTGCTATC[C/T]TTGTCTGGTTTGGTT | 57630 |
| rs757986420 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209775 | GCAATAAATGTTAAC[C/T]GCTTTTTCTTCATGC | 57630 |
| rs757992131 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211220 | GAGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57630 |
| rs757999763 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169269060 | AACAAGAGTCCTGCA[C/T]TCGGGACATCTGAGT | 57630 |
| rs758021334 | snp | C/T | 3.62194e-05 | 0.0042554 | missense | SH3RF1 | GRCh38.p7 | 4:169107198 | TTCAACAAACCCTTT[C/T]TTTCTTTCTGGAAAA | 57630 |
| rs758021722 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212591 | AAACTGAGCAGGAAG[C/T]ACAGAGAGTTCCCAT | 57630 |
| rs758043700 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162834 | CCAGCTCAAGAATGT[A/G]GGCTGACCAAGGCCA | 57630 |
| rs758070278 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195243 | AGATGTTGTTCCATT[A/G]CCTTCTGCTGGCTAC | 57630 |
| rs758134002 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167203 | ATCTTGAAAAGAAGA[C/T]GTTTGTATAGCCATG | 57630 |
| rs758144430 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | SH3RF1 | GRCh38.p7 | 4:169120961 | GTTCATCCTCTTTCC[A/G]AGGAGTGTATGGATA | 57630 |
| rs758154816 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241398 | TTCAGCCGAAAGGCA[A/G]TGAACTTCACCCCCA | 57630 |
| rs758172361 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215595 | TTGGAAGGCTATTAA[C/T]TACTGATTAAATCTC | 57630 |
| rs758190331 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153982 | AAAATATAGTAAACC[A/C]TTTTCATGCATCACA | 57630 |
| rs758223177 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121487 | AGTTCTAGGGAAAAA[G/T]ACTGAATTTGAAAAA | 57630 |
| rs758223822 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168030 | CTATAGTCCCAGCTA[C/G]TCAGGAGGCTAAGGT | 57630 |
| rs758235038 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226215 | TAAGTGAATGAAGAA[-/C]CCCCCCAGACAATGC | 57630 |
| rs758248082 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155849 | AAATTGCAACCTCAA[A/G]TGATACCTACCCTAG | 57630 |
| rs758249342 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156712 | GGATGAATTTTAATA[A/C]AATAATGGTCTTAAA | 57630 |
| rs758256366 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182292 | CTGACTTTTATATGC[A/G]AATCAGGTAAAATAC | 57630 |
| rs758263806 | snp | A/G | 1.78401e-05 | 0.00298659 | missense | SH3RF1 | GRCh38.p7 | 4:169136614 | GCTGCTTAGCAGCCG[A/G]GTTAAACTGCAAAAG | 57630 |
| rs758318601 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201798 | CCAATGTAAGTCAAA[A/G]ATTTACTATTAAAAA | 57630 |
| rs758323334 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195884 | GACAGAGTCTCACTT[C/T]GTTGCCCAGGCTGGA | 57630 |
| rs758347386 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148686 | AAGAATGGTACAAAC[A/G]GGGTACTGTAGAAGT | 57630 |
| rs758369832 | snp | A/G | 3.6863e-05 | 0.00429303 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122198 | AGCAGCGGCGGTGGC[A/G]CCTGGTGGTGTGGAG | 57630 |
| rs758381905 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096311 | ACAAGGCACACCTTA[C/T]ACATCCGAATCCAGA | 57630 |
| rs758425739 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159357 | TTTGAGGAAATAATA[A/G]TAAAACACAGCAATC | 57630 |
| rs758434266 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158433 | CTGGATAAGAATTAC[A/G]GAACATAAAGGAGAG | 57630 |
| rs758436922 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205388 | ACTAATTTATATTTT[C/T]GTAATCCCACTGATA | 57630 |
| rs758438562 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174540 | AAAGGGGAATCCAGT[A/G]TCAATCTCCTTCCCA | 57630 |
| rs758464453 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105587 | AGCCATACCCTTCTG[G/T]CTCAGGAAGAAGAAG | 57630 |
| rs758491478 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236361 | GGCTGGGTCTCTGAG[C/T]GACTCTAATGACTAT | 57630 |
| rs758516232 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111325 | AGTGGCATTAACATA[A/G]CTCACTGTAGCCTTG | 57630 |
| rs758523066 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262317 | TTGAATTTTTTTTTA[A/C]AACCAGAATGCTTTT | 57630 |
| rs758524803 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206400 | GGGCTGGGGGAAGGG[G/T]GGTGGTTCACACCCA | 57630 |
| rs758541491 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192241 | CTCAGGACATGAATA[-/G]GACAGTTCGCAAAAG | 57630 |
| rs758542194 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177732 | CTTTCAAGTTGCTTA[C/G]ATATATGTAAACAAG | 57630 |
| rs758564118 | snp | C/T | 1.65143e-05 | 0.00287348 | missense | SH3RF1 | GRCh38.p7 | 4:169122152 | GGTCAGTGGATCCTG[C/T]CATGGGCCTCGGTCC | 57630 |
| rs758593635 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139815 | TTACCTAACTTTGGG[-/G]CCTTAAGGGAGCCAT | 57630 |
| rs758594931 | snp | C/T | 1.75959e-05 | 0.00296608 | missense | SH3RF1 | GRCh38.p7 | 4:169156409 | CTACCTTTACCTTTG[C/T]AAATGGAAGGCAATC | 57630 |
| rs758611786 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192418 | GATCAGGGAAATGCA[A/G]ATGAAAACCATAATG | 57630 |
| rs758612925 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219838 | AATTATTTACATGTC[A/G]CCCTGTATGCAATCG | 57630 |
| rs758639295 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156527 | AAAGTTGGTGGGGAA[A/G]AAGCCATGGATTCCA | 57630 |
| rs758639691 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196684 | ATAACCTCTCCAATG[A/C]CTCCAAGCAGACTTT | 57630 |
| rs758643871 | snp | C/T | 3.65237e-05 | 0.00427323 | missense | SH3RF1 | GRCh38.p7 | 4:169106857 | CTTACCTTTCACAAA[C/T]GACAGGTCTAGACTC | 57630 |
| rs758644829 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242465 | TTTGGATGTATTTTT[C/T]TTCAAACATTAGTGT | 57630 |
| rs758666382 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229969 | CCAACACTTTAGGAG[A/G]TGGAGACGGGTGGAT | 57630 |
| rs758671950 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151629 | TAAACAAATGAGAAA[C/T]GTAGCCCTTGTTTCT | 57630 |
| rs758700575 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149672 | TCTTCCCAACTTACC[C/T]ACAATCTCCCTAAAT | 57630 |
| rs758754098 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217615 | CAGGGGTTCTGGACA[A/C]AGGAATAAGGCAAAG | 57630 |
| rs758784965 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123587 | TCAATTCAAAATATG[G/T]CACCATTAAGATTTG | 57630 |
| rs758866007 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231043 | TGCTAGGGCATAGGA[A/G]GGCTACTTACCTTCC | 57630 |
| rs758873714 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182834 | AGATAAGTTAGTAGG[A/T]AAAGAACTGCTTTCT | 57630 |
| rs758877288 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139504 | ATTTATCTATCCATT[C/T]TACTGCTGATTAACA | 57630 |
| rs758881915 | in-del | -/GAGAAGGGGCACTGCAGGAGAGCCCAGACA/GAGAAGGGGCACTGCAGGAGAGCCCAGACAGCTCGCTGATCCGTGCA | 4.95065e-05 | 0.00497506 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169130158 | TACTTATATGAACCT[lengthTooLong]GCCGAGAAAAGAAAA | 57630 |
| rs758924062 | snp | C/T | 1.65405e-05 | 0.00287576 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117500 | CTTTATCCTGATATG[C/T]TCTGGCCTGGGTTCC | 57630 |
| rs758943423 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266223 | TTCAATATACTTTGG[C/T]TAAACGCATGAGGAG | 57630 |
| rs758956504 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170160 | GGTTTACTAAGCCAG[C/T]TGCAGCAAGCCCAGA | 57630 |
| rs758956610 | snp | G/T | 1.80569e-05 | 0.00300468 | missense | SH3RF1 | GRCh38.p7 | 4:169136341 | GGGCACTGCAGGAGA[G/T]CCCAGACAGCTCGCT | 57630 |
| rs758959866 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219910 | TTTTGTCTCAAATGA[C/T]TAAAATGATACTTGG | 57630 |
| rs758960616 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184053 | GTAAGGAGGCTGGAA[A/G]GTGTTCACAAACAAT | 57630 |
| rs758993390 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163465 | GGCTAAGGGGCATTG[C/T]TTAGTAAATACCTAT | 57630 |
| rs759008629 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125185 | TACATCACTGAAGGA[G/T]CATGGCCTTTGGGGT | 57630 |
| rs759009448 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171820 | AATGTGGATGGCTCA[A/G]TATGATCTAGAAGAG | 57630 |
| rs759013706 | snp | A/G/T | 5.61187e-05 | 0.00529687 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130164 | ATATGAACCTGCCGA[A/G/T]AAAAGAAAAGTTATT | 57630 |
| rs759013793 | snp | A/C | 1.9585e-05 | 0.00312924 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269242 | CTGAGAAAAAATCTT[A/C]AGAAATGTTCATAGT | 57630 |
| rs759019582 | in-del | -/TCAGTC | 3.36717e-05 | 0.00410302 | cds-indel | SH3RF1 | GRCh38.p7 | 4:169096510 | TAAGCTTCTTCAGTG[-/TCAGTC]TCCTCATATGTTTTC | 57630 |
| rs759024445 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247395 | ACCTGGTCCAGGGGA[C/G]AGTGATGAACATGTG | 57630 |
| rs759045505 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242484 | AAACATTAGTGTGCA[C/T]AAAAATCTCCTGGGA | 57630 |
| rs759055766 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260182 | AATAGTCAGGGGCTT[C/G]AACTGACATACTGCC | 57630 |
| rs759071333 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216585 | GTTGCTCACCTCTAT[A/T]GTCCGAGAACTATGG | 57630 |
| rs759094993 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188836 | AGCTTTCAGCAAGGA[A/G]TGTTAAACACATGCT | 57630 |
| rs759126393 | snp | C/T | | | missense | SH3RF1 | GRCh38.p7 | 4:169156589 | CTTGTCTTCGCAAAA[C/T]GATGATGTCACCTTT | 57630 |
| rs759135306 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181695 | CTACTTTATGTGGAT[-/A]ATTAATACATTCATG | 57630 |
| rs759145576 | snp | C/T | 6.63967e-05 | 0.00576142 | missense | SH3RF1 | GRCh38.p7 | 4:169116469 | CTCGACTGATACTGA[C/T]GGCAGCAGTGTGCGT | 57630 |
| rs759202269 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235469 | CTATTATTATTTCCA[C/T]TTAAATATGAGCCAA | 57630 |
| rs759204560 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110894 | GATTCTGAAGTTATG[C/T]GTAGAAAATGGAAGC | 57630 |
| rs759213918 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203927 | GCTATGTGACCTTCA[A/G]CAATTACTTTTTACA | 57630 |
| rs759220453 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239528 | TTCAAAGTTAACTTT[C/T]ATCCAAGTTAACTTC | 57630 |
| rs759237533 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157841 | CTGCCTCCTGGGTTG[A/C]GTGATTTTAACGCTT | 57630 |
| rs759250930 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150890 | GAAAATTCTAAACTA[C/G]GTACAATCAAATAGC | 57630 |
| rs759258833 | in-del | -/AA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186850 | CTCTACTAAAAATAC[-/AA]AAAAAAAAAAAAAAT | 57630 |
| rs759266064 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193561 | CATTCCAAAATTGTT[C/G]CCTCTAGGACAAATA | 57630 |
| rs759269763 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209059 | CTTTGGGAGGCTGAG[A/G]AAGGTGATCACTTGA | 57630 |
| rs759269835 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161031 | AGGCTTTCCAAACTG[A/C]TGCTTTTCTTCTGTA | 57630 |
| rs759281547 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180247 | CCACGAAGAATAAAG[A/T]GGTATAGAAAAGAAA | 57630 |
| rs759325361 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146636 | AGGAGGAAAATTTCA[A/G]AGACTGGAGTGACCA | 57630 |
| rs759340812 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135751 | TAAACCTAAGAATAA[C/T]GCGTGGCTATTTTTT | 57630 |
| rs759357602 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194275 | TATTTGTCACAAAGG[C/G]AAACACTCATGGAAC | 57630 |
| rs759360184 | snp | C/G | 1.64857e-05 | 0.00287099 | missense | SH3RF1 | GRCh38.p7 | 4:169156624 | AATTTAAGGTCTCCA[C/G]GCTCTTTTCCTTCAT | 57630 |
| rs759409610 | snp | G/T | 8.24097e-05 | 0.00641857 | missense | SH3RF1 | GRCh38.p7 | 4:169156495 | GGGGGCTGAGGTAAC[G/T]GTTTAATAATCTGCA | 57630 |
| rs759412713 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261113 | TTCCCACAACCACTC[C/T]GCATGGAGCTTAGGT | 57630 |
| rs759424767 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134607 | GTGAGTGGCCATCTT[C/T]ACTAGCTCCCTCCTT | 57630 |
| rs759437496 | snp | A/G | 3.29723e-05 | 0.00406018 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117659 | GGGACTCCCAGCCAC[A/G]CCATTTCCCTGGAGC | 57630 |
| rs759508987 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121301 | CCTAACTTGCTACCA[A/G]AGATTATGTACCCAC | 57630 |
| rs759548710 | snp | C/T | 5.71271e-05 | 0.00534418 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106823 | TCATTTTTTAGTTTT[C/T]TCCTGGAACGAAGTT | 57630 |
| rs759552702 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215534 | GGTATAATTTCTTCC[C/T]TCAGTGTTTGGTAGA | 57630 |
| rs759562029 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248939 | AGGGCCTTTAAGAGG[C/T]AATTAGGGACGGGCC | 57630 |
| rs759581918 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195402 | TGATATGTCTAGGTA[G/T]GAGTTTCTTTTTTAT | 57630 |
| rs759605281 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104837 | ACCCGGGAAATGGAG[A/G]TTGCAGTGAGCCAAG | 57630 |
| rs759619298 | snp | G/T | 1.64882e-05 | 0.00287121 | missense | SH3RF1 | GRCh38.p7 | 4:169268948 | TGCAGTTGGTCCCAC[G/T]TCCCCCACCAGGACC | 57630 |
| rs759628778 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244033 | TGAGGTTTTGAACTG[A/C]ATTCCTGTTCATTTC | 57630 |
| rs759661396 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154008 | TCACAAACCAAGTAT[C/G]AGCATGTAATATTGA | 57630 |
| rs759668347 | in-del | -/AGAATAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218320 | TAGAATATAGAATAT[-/AGAATAC]AGAATACAGATTATA | 57630 |
| rs759716006 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183866 | GCTAAAATACTAGAA[A/G]TGTAGGAAAGAGACT | 57630 |
| rs759718427 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232101 | GCATACAGGAACTGG[C/T]TTAGAGCATTTTAAA | 57630 |
| rs759739179 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172334 | TCATGAGTAATTCCT[C/T]CTTATTTTAAGAATA | 57630 |
| rs759739902 | snp | G/T | 1.79632e-05 | 0.00299687 | missense | SH3RF1 | GRCh38.p7 | 4:169268842 | GGGGGGCTCCAGGAT[G/T]GCACCCGAGGCTGCT | 57630 |
| rs759756611 | in-del | -/GT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166112 | AAATTGAAAAATTAG[-/GT]GTTCAACAACAAAAG | 57630 |
| rs759828316 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166878 | AATTGGTATCTGCAA[C/T]GTAAAAATCTCAAAA | 57630 |
| rs759867419 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159186 | TGGTCATTCACAACG[C/T]TGTGTACTCTGGTCA | 57630 |
| rs759870010 | snp | A/C | | | missense | SH3RF1 | GRCh38.p7 | 4:169155518 | TTCCTATTTTGTCTG[A/C]CAGCATTCCTTCAGC | 57630 |
| rs759870407 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225213 | CAAAGCATCATGAAA[A/G]GAGAAGAGGATTTGA | 57630 |
| rs759888466 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126541 | TCTGACATTCAACTT[G/T]GTTTAAATACACACA | 57630 |
| rs759908004 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224152 | AACACTCCTATGAGG[C/G]ACAGGAAGCAGGCAG | 57630 |
| rs759910404 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097990 | AAGTGATGTGAATAA[C/G]CCATCTTAGAAGGGG | 57630 |
| rs759915820 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176885 | TGTGCTGGGCATGGT[A/G]GCTAGGATTAAAGGT | 57630 |
| rs759919524 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121798 | TTTGTGAAGAATACC[-/T]TTCTGTCACTAGTAT | 57630 |
| rs759939053 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131283 | GTATCTATTAGTCTA[C/T]ATATTGATTGAACTA | 57630 |
| rs759955258 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131203 | ATCAGCATCATGGCA[C/T]GTAATTTATTTTCAC | 57630 |
| rs759958427 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212387 | AATTTCTAAAAGATT[A/C]TCTGAAATATTTAAT | 57630 |
| rs759980934 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242710 | ATGGACTGTCCTTTA[C/T]GAAGGGAGTGGGTTT | 57630 |
| rs759994143 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114320 | TTCACCATCACGTCT[-/C]CCTTCTCTGGCCCTA | 57630 |
| rs760001517 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163788 | CCACCAAAATTCATC[A/G]AGAACAGTCCATTTC | 57630 |
| rs760006295 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263157 | ACAACTCCTTTGTCC[A/G]TCAGTGTTTGTAGTG | 57630 |
| rs760016593 | snp | A/T | 1.81949e-05 | 0.00301614 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136649 | CAACAAACCAACACA[A/T]GAAGGTTAAACAATT | 57630 |
| rs760038158 | snp | A/G | 1.70159e-05 | 0.00291679 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096496 | GTGTGAAGTGATTTT[A/G]AGCTTCTTCAGTGTC | 57630 |
| rs760047138 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116709 | CATGAGTCATTTCAC[C/T]GCATCAGACCATGAT | 57630 |
| rs760058147 | snp | A/G | 3.68922e-05 | 0.00429473 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136669 | GTTAAACAATTCCTA[A/G]GAATTCCCTGAGGTT | 57630 |
| rs760060910 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200943 | GTAAAATGACAGCAG[C/T]AAGAGAACAGAAGTC | 57630 |
| rs760085347 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103891 | AAATTTAAATGGTTA[C/T]ACAAAAAAACCTATC | 57630 |
| rs760090960 | in-del | -/CCAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255690 | GATCAACTGACCCAC[-/CCAT]CCATCCATCTATCCA | 57630 |
| rs760097210 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121650 | TGGTGTATAAAATTA[C/T]ACAATGCAGGATCCA | 57630 |
| rs760101038 | snp | C/G | 1.70055e-05 | 0.0029159 | missense | SH3RF1 | GRCh38.p7 | 4:169136560 | AGGAACATTCTCCAG[C/G]ATCAACTCCTGGCAC | 57630 |
| rs760112889 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196447 | GGTAACGATGTACTA[C/T]ATTTTTTATGGTGTG | 57630 |
| rs760121780 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180975 | AACCCTTTCTTTTCT[C/T]TTTACTCACAAATTC | 57630 |
| rs760161719 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180104 | CCAGTGCTGAACAGC[C/T]AAAGCCAGACCATCT | 57630 |
| rs760180888 | snp | C/G | 1.65285e-05 | 0.00287471 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169120833 | CCTTGTGACTGGTGC[C/G]ACATAATTGCCAGGG | 57630 |
| rs760188161 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213946 | TCTTGAAGTTGGATG[A/G]TGTGAGTCCTCTTTG | 57630 |
| rs760221409 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228023 | ATAAAAGCAACATAA[C/T]GCATTTTTAACTACT | 57630 |
| rs760284552 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166655 | GCTGCTGAGCCACAG[C/G]AAAAACCTTCAGTCA | 57630 |
| rs760298967 | in-del | -/CCCCTCACTGGGGGGCTCCAGGATTGCACCCGAGGCTGCTGTCCG | 8.38511e-05 | 0.00647445 | cds-indel | SH3RF1 | GRCh38.p7 | 4:169156677 | GGTAACTGAGGTATA[lengthTooLong]CCCTTTAAAAAAAAA | 57630 |
| rs760314595 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262341 | TGCTTTTACATACAT[C/T]TTGAAATCTACATTC | 57630 |
| rs760328001 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209628 | AAGTAAACAATATAA[A/G]TTCAAACCCTGGTCC | 57630 |
| rs760338389 | snp | A/G | 6.64673e-05 | 0.00576448 | missense | SH3RF1 | GRCh38.p7 | 4:169116483 | ATGGCAGCAGTGTGC[A/G]TGGCTGAGCCTGGCA | 57630 |
| rs760354408 | in-del | -/AA/ATATAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174002 | AATTTCCTGAGTTAT[-/AA/ATATAC]ATATATATATATATG | 57630 |
| rs760370770 | snp | C/T | | | missense | SH3RF1 | GRCh38.p7 | 4:169155553 | TTTTCATCCACTCTT[C/T]GGATCACAGTCAGAA | 57630 |
| rs760372584 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167770 | TAAATATATTCTGTA[C/T]CTTGACGGAGGTGTT | 57630 |
| rs760416618 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221593 | TGCATTAGGCTAAAA[C/T]GTTCTTTATGATAGC | 57630 |
| rs760424047 | snp | A/C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193403 | TGTTAGCTTCCAACA[A/C/G]ACAATGCACAAGGAC | 57630 |
| rs760532008 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112473 | TGATTTTTAAATGTT[C/G]AAAGAAAATATATGC | 57630 |
| rs760548362 | snp | A/C | 1.87566e-05 | 0.00306235 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268799 | CCTTTATTCACCAAA[A/C]TACCTCTGTAGGCTA | 57630 |
| rs760549480 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112714 | ACATAACGTGGCCCA[C/T]AGCAATTCAAGAAGG | 57630 |
| rs760556227 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162621 | TCAAAACTACCAGCA[C/G]TTTGAGGATGGCAGC | 57630 |
| rs760608624 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156998 | TGACTGCCAGGTCTG[-/C]CTCTCAAGAACTCAT | 57630 |
| rs760611917 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237739 | GTAAAGATGAATACA[C/T]ATTACTGATAAAGAA | 57630 |
| rs760621229 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258273 | TCATGCTTCATATAT[A/G]GAGACCCAGTACTTT | 57630 |
| rs760621818 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113515 | AAAGGGAAATAAAAC[C/T]CTTCCAGGAGACACT | 57630 |
| rs760639487 | snp | C/T | 5.0491e-05 | 0.00502424 | missense | SH3RF1 | GRCh38.p7 | 4:169107010 | CAGTCGTGACCGGTC[C/T]GTCCCCGTCCACAGG | 57630 |
| rs760649621 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150675 | TCTACATGCATCTTA[G/T]GGCCCCATGTCCGAG | 57630 |
| rs760649747 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133987 | ACGCACTGATCTCCA[C/T]GGTTGGAAGAGTTTT | 57630 |
| rs760672957 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162380 | TTCAACTTCAATGAC[A/G]GCCAAGACGAATATT | 57630 |
| rs760683679 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152368 | CCCTACTCACTTCTC[C/T]CAACCAGACTCTCCT | 57630 |
| rs760702021 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226994 | CAACATAACAAGACC[C/G]CATCTCTATAAAAAG | 57630 |
| rs760702135 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239197 | ATGTGGATAGCCATT[G/T]CTGCCAAGATTGTGC | 57630 |
| rs760721489 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211481 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs760727741 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267109 | GTTCAATTTTGGGAG[C/G]TTAGCAGTTCAGATA | 57630 |
| rs760754329 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102350 | TATCCAATTTGTATG[C/T]TTCCAAGTGTTCTAG | 57630 |
| rs760764279 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177851 | TACATATGTGTATGT[A/C]TATAATATATATATA | 57630 |
| rs760788969 | snp | C/T | 3.73448e-05 | 0.00432099 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269219 | TTCATCCATCTTTAT[C/T]TACTTTACTGAGAAA | 57630 |
| rs760813044 | snp | C/T | 1.81296e-05 | 0.00301072 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136299 | GCTCTTTTTATATAA[C/T]ACTTGTTTGAGGATT | 57630 |
| rs760818850 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251064 | CAGGACTCAGTTATG[C/T]GACTGAAGTCTAATG | 57630 |
| rs760820381 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157608 | GCGCTGTTGCATATC[A/G]TTGATTCAGGAGATA | 57630 |
| rs760822592 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163651 | TAAATCACATTAATG[A/G]TCTAAATCATGAGTT | 57630 |
| rs760853345 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196146 | AGTCTATTTCTATAA[C/T]GCCAATCTATGAAGC | 57630 |
| rs760864361 | snp | C/T | 6.33961e-05 | 0.00562975 | missense | SH3RF1 | GRCh38.p7 | 4:169130148 | TAACCCGGTGGTACT[C/T]ATATGAACCTGCCGA | 57630 |
| rs760894415 | snp | C/T | 1.65116e-05 | 0.00287324 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169096675 | AGGAGGATAGGAAAC[C/T]ACCACCCTGTGCCTA | 57630 |
| rs760896762 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230621 | CCCATCACTTTGGGA[A/G]GCCAAGATGGGCAGA | 57630 |
| rs760910548 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152892 | AGGGCAAACTATTCC[A/G]GTAGCATTTCTCACC | 57630 |
| rs760930784 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137595 | GTGATTTTTCCATCT[C/T]GGCATTACACATTGG | 57630 |
| rs760968595 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203741 | AAATAACTGTGAAAC[A/G]AATGACTGAATAATC | 57630 |
| rs760978744 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160479 | TAGGGTTACATTTCC[A/G]TGATGCAACTGAAAA | 57630 |
| rs761002392 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235271 | CCTTACAGACTAAAC[G/T]CGTCATCAAAGTATT | 57630 |
| rs761019231 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138973 | TGGGGGGACTGGGGG[G/T]AAAGGTCTCACTCTG | 57630 |
| rs761042978 | in-del | -/AAAAAA/AAAAAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197623 | AGCAAGACTCTGTCT[-/AAAAAA/AAAAAAA]CAAAAAAAAAAAAAA | 57630 |
| rs761049356 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146561 | AAGAATAGTGGTAGA[C/T]GTTATTGAGAGGACA | 57630 |
| rs761057276 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | SH3RF1 | GRCh38.p7 | 4:169120906 | CAGCCATCCTGGCAG[C/T]GCTCAAACACTAAAA | 57630 |
| rs761062176 | snp | A/T | 1.85002e-05 | 0.00304134 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116236 | ACAGGGAAGTAAGTA[A/T]AGCAGAGAAACAGTA | 57630 |
| rs761062243 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174268 | GGTCTCTCTATGTTG[A/C]CTAGGCTGCTCTCAA | 57630 |
| rs761064842 | snp | C/T | 1.64836e-05 | 0.0028708 | missense | SH3RF1 | GRCh38.p7 | 4:169268962 | CTTCCCCCACCAGGA[C/T]CAGGTTTCCAAGGCC | 57630 |
| rs761066841 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234583 | CAAACTTCTAACACT[A/G]GACTTGCCATTTAAT | 57630 |
| rs761086336 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261705 | AAAACCACAAGTTGC[A/G]GAACTGCATATACAA | 57630 |
| rs761090394 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095604 | TGTGTCCTGGGCATG[C/T]AGGTCAGTTGGGGTA | 57630 |
| rs761100040 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105389 | GGTAGCTATTTGTCT[C/G]ATTAAATAATATATT | 57630 |
| rs761118008 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144736 | TGCTTTCTTTCAATG[A/G]GCAACTACTTGGCAG | 57630 |
| rs761139187 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131065 | CCAAACATAGTTTTC[C/T]CAGTTCCCACACATT | 57630 |
| rs761146142 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175682 | TGACATTTATCATGA[C/T]TAGGCACCGACCCAC | 57630 |
| rs761180351 | snp | A/C/T | 3.42825e-05 | 0.00414009 | missense | SH3RF1 | GRCh38.p7 | 4:169107169 | TCCGTTTAGTGGAGG[A/C/T]GCCAGAAAGCAACTT | 57630 |
| rs761192523 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237569 | TTGACCACCAGCATG[C/T]TAAAAATATGAATTT | 57630 |
| rs761194305 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096979 | TTTGTATCTTGGCCA[C/T]AAAGGAGAGTTTCAT | 57630 |
| rs761219938 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115453 | GAACCCTATTGTGAA[A/C]TGCACATGCGAGGGA | 57630 |
| rs761220238 | snp | C/T | 1.65364e-05 | 0.0028754 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155605 | AATCATTAATCTACC[C/T]GATCATTAAGCTGTA | 57630 |
| rs761229365 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242738 | TTTGTTATAAAAGCG[C/T]GTTTGGCCCCCATTG | 57630 |
| rs761266294 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209484 | CTCGTGGGCTGTAAT[G/T]AAATAGTTAACAGTC | 57630 |
| rs761269643 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254230 | TTCCATCAAGAAGTA[C/T]TTACTGAACTGACCA | 57630 |
| rs761275650 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148237 | ACTAGGGCAGGGCAG[A/C]AGTCTAGGGAAGCGA | 57630 |
| rs761284255 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226924 | GTAATCCCAGCACTT[C/T]GGTAGGCTGAGGTGG | 57630 |
| rs761294551 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223126 | GGACCTTCCTGGGGC[C/T]TTTCTGCCAGGAAGA | 57630 |
| rs761311846 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126623 | TAGGAACAGCATCTA[A/G]TCCTGGCTGGAGTGC | 57630 |
| rs761313695 | snp | A/G | 1.80494e-05 | 0.00300406 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156355 | TTTCTATGTATCTGG[A/G]TACAGAGGTAGAGCT | 57630 |
| rs761319651 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166701 | CGAGCCAGCATCACC[C/G]CAGGGACCATTCTGA | 57630 |
| rs761326380 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149151 | TCTCAGCTCTCTCAA[C/T]GTTTTCCTGATGGAA | 57630 |
| rs761402058 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132660 | GTTGTCTCCTCTGCA[A/T]GAAAGGCTAAGTAAG | 57630 |
| rs761425186 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169119125 | TTTTTTTTCCTTAGG[A/G]TGGAGTCTTGCTCTG | 57630 |
| rs761427922 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268739 | CAATGAGTTGACTTC[A/G]AAAACACCAAGCTAA | 57630 |
| rs761438138 | snp | A/C | 0.00020272 | 0.0100657 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155448 | AGTAAGCTGAATATT[A/C]ACACAGTTCAAGTTT | 57630 |
| rs761441533 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154315 | CCCATGGATATACAG[C/T]AGTCAAATTGATTTT | 57630 |
| rs761454735 | snp | C/T | 1.68892e-05 | 0.00290591 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096716 | AGATTTTGGTTAAGG[C/T]GATTCAAAGCAGTGA | 57630 |
| rs761456720 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213718 | GTCTGTTTCTAGATT[C/T]ATTGTTTGCATTTGA | 57630 |
| rs761471505 | snp | A/C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191629 | TGGAGGCATCACATT[A/C/G]CCTGACTTCAAACTA | 57630 |
| rs761501394 | in-del | -/AT/CATA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255613 | ACATACACACATACA[-/AT/CATA]TACACACATACACAC | 57630 |
| rs761532590 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239859 | ACCCCGTCTCTAATG[-/A]AAAAAAATACAAAAA | 57630 |
| rs761560162 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204663 | TTGAGTGATTCACCT[A/G]CCTCAGCCCCCTGAG | 57630 |
| rs761576669 | snp | G/T | 3.43708e-05 | 0.00414538 | missense | SH3RF1 | GRCh38.p7 | 4:169130101 | AACGAGGGGCCAGTT[G/T]TCACTGGGCTGCTTG | 57630 |
| rs761578385 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256511 | CTGTTTAAAACAGAA[C/T]GAAATGTTCTATGGT | 57630 |
| rs761592907 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111200 | CCACTACTTGGGAGG[C/T]TGAGGTGGGAGGATT | 57630 |
| rs761594492 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166486 | CATGTACAAGAGGAA[G/T]TACTCAGCCAATAAA | 57630 |
| rs761638462 | snp | C/T | 0.00014967 | 0.00864942 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116667 | CACAGCAAAATTCAA[C/T]TATCTAATAGATGCT | 57630 |
| rs761643252 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257981 | AAATGTGAGAGCCAC[A/G]TGTCACCTCAATGCA | 57630 |
| rs761659577 | snp | C/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271791 | GGTAGTACGGACTTC[C/G]AACCCAGGCTCGGGG | 57630 |
| rs761674822 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182024 | GTATCTTCAGGGTCT[A/G]GAGCTATGCCCAGCA | 57630 |
| rs761680843 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098203 | GCAACAGATATCTAA[G/T]AAATACATCTTTCAC | 57630 |
| rs761682823 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116144 | ATAGTGACTCACACG[C/T]AGGGAGCACCTGAGG | 57630 |
| rs761706442 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159010 | GTCCTGGGAAGACAG[C/G]GGTTGAGCCTTCCAG | 57630 |
| rs761737876 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152724 | CCTGCGCAACAAGAG[C/T]GAAACTCTATCTCAA | 57630 |
| rs761749208 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270634 | CTGCGCCCGGGGAGA[C/G]CGCGGCACGGAGCCC | 57630 |
| rs761750491 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207820 | ACTCAGCAGAGGACA[A/G]GAGACAGTTGTTTAT | 57630 |
| rs761779590 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126047 | TGAGAGATGGAGTTA[A/G]TAATTAGAAATAGTT | 57630 |
| rs761784293 | snp | A/G | 8.73401e-05 | 0.00660775 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122297 | CATAAAGAGAAAGGG[A/G]AAAAAGGGAACAAAA | 57630 |
| rs761796366 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159966 | TCACTGACATGTACC[A/G]TTTAATAGGGGATGG | 57630 |
| rs761825014 | snp | C/T | 1.69542e-05 | 0.0029115 | missense | SH3RF1 | GRCh38.p7 | 4:169106929 | GTGGAGCGATGGGAA[C/T]TGCGGAGTCCAGGGA | 57630 |
| rs761829524 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236820 | TAAAATGCTACATAT[C/G]TAGGCTCAAAGGCTA | 57630 |
| rs761829580 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214174 | TAGCTTGGTACTGTC[C/G]TTGCAATAATGAGTG | 57630 |
| rs761833603 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112393 | AGAAATATTGAGAAC[G/T]TGGAATAAAGCATGG | 57630 |
| rs761876655 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147912 | TAAAGCTTTAGTTAC[C/T]GGAAAAATTTAGTGT | 57630 |
| rs761884790 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201853 | GAAAACCCATCTGTC[A/G]TCGCTACAGAGGCAA | 57630 |
| rs761897527 | in-del | -/CTCA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131437 | CTTATTAGACAGAGT[-/CTCA]CTATGTTGAGCAGGC | 57630 |
| rs761918531 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230726 | TAGCTGGGCGTGGTG[A/G]CACACACCTGTAGTC | 57630 |
| rs761943769 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134114 | ACCTCGGCTGGAGAA[A/G]CCAGGCAGCACTTCA | 57630 |
| rs761948495 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138039 | TGAAGTACCAATGGC[A/G]GGAGAAAGATCATAA | 57630 |
| rs761951396 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239884 | CAAAAATAAGCCGGG[C/T]GTGGTGGTGTGCACT | 57630 |
| rs761978674 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175610 | AATAGCCTCAACCCA[A/G]CCAGCACCCAACACA | 57630 |
| rs762000567 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | SH3RF1 | GRCh38.p7 | 4:169117571 | TCATTTGCCCCGTCA[C/T]GTGCAACAAGACCTT | 57630 |
| rs762040861 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228772 | GTACACTTTCTATTT[G/T]ATTTTTCATACAGAC | 57630 |
| rs762090875 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194326 | GAGTTTGCCAGAACC[C/T]AGAAGTGTGCCTTAT | 57630 |
| rs762098178 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151126 | ATAAAAGTTCATAGG[C/T]TGCTCATTCATTCAA | 57630 |
| rs762121261 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102019 | TTCTAGCCTCTCTGG[C/T]GTTCTCTGTAGTTCA | 57630 |
| rs762146857 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246892 | TTGCAAGACTGCTGT[A/G]GAAAGAAAAACTTGA | 57630 |
| rs762150238 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151465 | GTAGTAGAGTCAAGA[C/T]TGGAATCCTGGCCAT | 57630 |
| rs762153442 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105492 | AAGGCTGGAATCACT[-/A]AAACAGGGCTTATTA | 57630 |
| rs762196870 | snp | A/G | 1.80837e-05 | 0.00300691 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136312 | AACACTTGTTTGAGG[A/G]TTTACCTGAGAAGGG | 57630 |
| rs762203525 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201246 | ACCACGGCCTCTCCA[A/T]CTACTGCCAGAGCTG | 57630 |
| rs762206071 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248656 | ACTTCAAGTAAAATT[G/T]TAAAAAATTCAAAAA | 57630 |
| rs762211268 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245553 | AAAACAAAGCTCCAA[C/T]TGGTCTAACATCATC | 57630 |
| rs762223268 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176983 | ATGTTGCCCGGGTTG[C/G]TCTTGAACTCCTGGC | 57630 |
| rs762249943 | snp | A/G | 1.91492e-05 | 0.00309423 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269231 | TATCTACTTTACTGA[A/G]AAAAAATCTTCAGAA | 57630 |
| rs762258594 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142899 | TATTCTTCCCTACAA[C/T]TTAGGTAATAAGGTT | 57630 |
| rs762266035 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106458 | ACAACTAGCAGGAAA[C/T]GATGTAAATTTTTAA | 57630 |
| rs762272929 | snp | C/T | 3.29799e-05 | 0.00406065 | missense | SH3RF1 | GRCh38.p7 | 4:169122109 | ACTTACACACTGGGG[C/T]GAGTCTGCGGCCGTA | 57630 |
| rs762278677 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185030 | ATCAGGGGTTATCTG[C/G]TTCCTAGAATGGAGT | 57630 |
| rs762293008 | snp | C/T | 1.65449e-05 | 0.00287614 | missense | SH3RF1 | GRCh38.p7 | 4:169116379 | TCCGGCCACTGGGCT[C/T]AGCCTCCAGAGAAGC | 57630 |
| rs762308021 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122053 | TCTGAGGTTTGGACT[A/T]CGTTTAAATGAACAC | 57630 |
| rs762328167 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251261 | CAGGGAGGGTGGAAG[A/G]TAGGAAACTACTTTT | 57630 |
| rs762329258 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233186 | CCCAGGAGGCAGAGG[A/T]TGCAGTGAGCCAAGG | 57630 |
| rs762346484 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128428 | GGAAACATTAAAAAC[A/G]AAAATAAAACAAACA | 57630 |
| rs762355790 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108088 | GTGCTCCTTCATTCT[A/G]AAACCTTAAGCGTGA | 57630 |
| rs762384694 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221161 | AAGAGTAATCCTCAA[C/T]AGCATTAAGACGAAA | 57630 |
| rs762385773 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158916 | TATTGCTCTCAAAAT[G/T]CTATTGGCAATCATC | 57630 |
| rs762392771 | in-del | -/G | 0.00011573 | 0.00760603 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120998 | AACATACCTAGAATA[-/G]AAAATAATATTTGAT | 57630 |
| rs762395799 | snp | A/G | 1.65364e-05 | 0.0028754 | missense | SH3RF1 | GRCh38.p7 | 4:169116391 | GCTCAGCCTCCAGAG[A/G]AGCACTGGTGATGCT | 57630 |
| rs762401136 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266577 | TGAAAGCAAAAGGTA[C/G]TAGTAACTTACTGAG | 57630 |
| rs762432845 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236600 | TAGTAGCAACTACTT[C/T]GTAGTGTTGCTATGA | 57630 |
| rs762439184 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197855 | TATCCCTTTAAAATA[C/T]TACTAAAAGTGGACT | 57630 |
| rs762487148 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272381 | TCATGCATCAGTTCA[A/G]TTCTCTCAGCAACCC | 57630 |
| rs762498662 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167963 | ACAAAATAGTGAGTC[C/T]CTGTCTCTAAATAAA | 57630 |
| rs762502342 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177029 | TACCTTGGCATTCTT[C/T]AGGAGGCTGGGATTT | 57630 |
| rs762503042 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204012 | TAATCTTGGCACATC[A/G]AAGGCATTCAAAAAA | 57630 |
| rs762526128 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146865 | ACTGACATGCAAAAC[A/G]GTAAAGATATAATAG | 57630 |
| rs762538840 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098136 | AAGTGTGAAATAATA[C/T]ATGCTTATTATTGTT | 57630 |
| rs762592521 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190486 | GAGGAGATGGATAAA[C/T]TTCTAGAGAGATACA | 57630 |
| rs762598303 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195996 | TTTTTATATTTTTAG[G/T]AGAGACAGGTTTTTG | 57630 |
| rs762605612 | in-del | -/CAAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230855 | AGTGAGAAACCACCT[-/CAAA]AAAAAAAAAAAAAAA | 57630 |
| rs762614408 | snp | C/G | 1.80383e-05 | 0.00300314 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156366 | CTGGGTACAGAGGTA[C/G]AGCTGGCAAACAGAA | 57630 |
| rs762616990 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261380 | TCTGCCAGCTGCAAC[G/T]GAGAAAAGATTCCCC | 57630 |
| rs762646386 | snp | C/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240237 | GGTCTCACTCTGGCA[C/G/T]GCAGGCTGGAGTGCA | 57630 |
| rs762646698 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | SH3RF1 | GRCh38.p7 | 4:169156489 | TGAGGTGGGGGCTGA[A/G]GTAACGGTTTAATAA | 57630 |
| rs762647098 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243189 | CACAATAAAAATACC[-/A]AAAGGCAAGGCATAT | 57630 |
| rs762670411 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217558 | ACTAGAGACAGAAAG[A/G]AAAGCCTAAACCTGA | 57630 |
| rs762702252 | in-del | -/CA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153507 | CTTAAGAAAAAGCCC[-/CA]GTTTTTATTCCTATA | 57630 |
| rs762712694 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269387 | AGGAGCCAAGAATCA[A/G]AAAGTACCCAAAAGT | 57630 |
| rs762718410 | snp | A/G | 1.64817e-05 | 0.00287064 | missense | SH3RF1 | GRCh38.p7 | 4:169117543 | CTCACAGCATTGCGG[A/G]CCTGGTTGACTGTCA | 57630 |
| rs762766413 | snp | A/T | 3.41956e-05 | 0.00413481 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096735 | TCAAAGCAGTGATTT[A/T]AAAAAATGGTGTACT | 57630 |
| rs762768768 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182395 | ATGTGTTTCAGCACA[C/T]ATATAATTAAGAATG | 57630 |
| rs762778939 | in-del | -/A | 1.69742e-05 | 0.00291321 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120788 | AGCTTCTCTGTTTAG[-/A]ACATAGTAAACAATG | 57630 |
| rs762872631 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184904 | TGTCTGTGAGATAAA[C/T]GGTTTTATTTCCTGA | 57630 |
| rs762895708 | snp | C/T | 1.648e-05 | 0.0028705 | missense | SH3RF1 | GRCh38.p7 | 4:169096568 | CCAGTTTTCCCATTA[C/T]GTTGTAATGTGCCTT | 57630 |
| rs762904420 | in-del | -/AG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159376 | AACACAGCAATCGAC[-/AG]AGAGAGAGAGATAGA | 57630 |
| rs762905725 | snp | A/G | | | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169271083 | AGGAGGAGGAGGCCG[A/G]GACGCAGCCGGCGCC | 57630 |
| rs762906763 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138896 | TACTGGGTGCTTCCT[C/T]TGTGTCTTTCTTCAT | 57630 |
| rs762920934 | snp | G/T | 1.66015e-05 | 0.00288105 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117478 | TCTACTATTAGGCAG[G/T]TAAGCCCTTTATCCT | 57630 |
| rs762924499 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109603 | TTTCTATGTTAGCAG[A/G]AGAATGTTCCACTTG | 57630 |
| rs762952022 | snp | C/T | 5.08315e-05 | 0.00504115 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169156681 | AACTGAGGTATACCC[C/T]TTAAAAAAAAAAGAG | 57630 |
| rs762972204 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248353 | GGGACATGGATGAAG[C/G]TGAAACCATCATTCT | 57630 |
| rs763005689 | snp | C/G/T | 0.000269568 | 0.0116068 | missense | SH3RF1 | GRCh38.p7 | 4:169107022 | GTCCGTCCCCGTCCA[C/G/T]AGGGCAGGAGCCTGC | 57630 |
| rs763017088 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158121 | TTCTTAAAGGATATT[A/G]GTAATAACTACAATA | 57630 |
| rs763019219 | snp | C/G | 1.68707e-05 | 0.00290432 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107146 | TGCTGGAGGAGACAC[C/G]CGGGGCTTCCGTTTA | 57630 |
| rs763032877 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142683 | ACTTCAACATTCTAC[C/T]GCATCACTAAGTCCA | 57630 |
| rs763050842 | snp | A/T | 5.32014e-05 | 0.00515731 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117829 | AGTCCATCAGCAAAA[A/T]GACAGAAAGAACAAT | 57630 |
| rs763055934 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109269 | AGCCACAGCTAAAGC[A/T]GTTTCTTAAAAGCTC | 57630 |
| rs763107815 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177823 | TAGTTTCCTTATATT[G/T]GAATGAAAACCTTAC | 57630 |
| rs763143439 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138907 | TCCTTTGTGTCTTTC[G/T]TCATATCATATATTC | 57630 |
| rs763144561 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172375 | TGGATATACCTGTAC[G/T]CAGAAAATATCTTCG | 57630 |
| rs763147364 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095047 | TGACTGCGTGGCACC[A/G]TAATGAAATCGGTGG | 57630 |
| rs763163408 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163869 | TGCATTTCTTTCACT[C/T]GGATTTTTATGTCTG | 57630 |
| rs763164689 | in-del | -/CTC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198325 | ATTAATATTAGTGTT[-/CTC]CTTCTGTACTGCAAA | 57630 |
| rs763181269 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232875 | CCTAAACTCTGAACA[C/T]ATAATCTACTAGTCT | 57630 |
| rs763183336 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205113 | AAGGGAAATAGCTTC[A/C]TTAAATGAACTATTT | 57630 |
| rs763194416 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128222 | GGGAAGGAAAGGAGA[C/G]AGTCTCCCCTGGAGA | 57630 |
| rs763218681 | in-del | -/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204551 | ATATATTACCTTCTC[-/TT]TTTTTTTTTTTTTTT | 57630 |
| rs763220512 | snp | C/T | | | missense | SH3RF1 | GRCh38.p7 | 4:169120960 | AGTTCATCCTCTTTC[C/T]GAGGAGTGTATGGAT | 57630 |
| rs763247422 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173923 | AATAAGATCACCCTA[A/C]CCACACACCACCACT | 57630 |
| rs763257141 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212577 | TTAGGTTCACAGCAA[A/T]ACTGAGCAGGAAGTA | 57630 |
| rs763271047 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153077 | CCTAGGAGAGTTCCT[C/T]GGGCATATCCATTAC | 57630 |
| rs763280912 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113592 | TCTGTGGATGGGAGG[A/G]TGATGTAAAAGGCAG | 57630 |
| rs763293902 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124568 | GAAACATAAATGGTT[C/T]AATACAATTGGGCAG | 57630 |
| rs763312192 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178078 | AAACCCTGTCTCTAC[C/T]AAAAATACAAAAATT | 57630 |
| rs763336085 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161586 | AATGCCCAGATGTAC[A/G]TGCAAGACAGCCTCT | 57630 |
| rs763348745 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213140 | TGACTGTACCATTCT[C/G]CATTTCCACCTGCAA | 57630 |
| rs763355777 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199705 | CTTCCAATCCACTGG[A/G]AATAAGAAAACAAAC | 57630 |
| rs763358464 | snp | A/G | 1.68202e-05 | 0.00289996 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136549 | GGCTGCTGCCGAGGA[A/G]CATTCTCCAGCATCA | 57630 |
| rs763384433 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232180 | GGCAAGAAAGGATAT[C/G]AGACCCAACAGGCTC | 57630 |
| rs763393076 | snp | A/G | | | stop-gained | SH3RF1 | GRCh38.p7 | 4:169117604 | CCTGAGGACTTGTCT[A/G]GATGTGAGCTGCTGA | 57630 |
| rs763395108 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133649 | CGGGTGTGGTGGTGG[C/T]GCCTGTAATCCCAGC | 57630 |
| rs763402226 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165391 | TTAGTATTAAAGAGG[C/T]TGGGTAACAGCCACA | 57630 |
| rs763411961 | snp | C/T | 1.66101e-05 | 0.0028818 | missense | SH3RF1 | GRCh38.p7 | 4:169136458 | AGGACTTGTTGGCCA[C/T]AGTGAGGGAAGTGAA | 57630 |
| rs763414529 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198753 | AGACAAAGAGAAGAC[C/T]TTACAAGAGAAAAAA | 57630 |
| rs763441406 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250276 | GAGCTAAAAACAGAG[A/C]TGCTGCTATGGTTTG | 57630 |
| rs763465466 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130427 | GCCATTGGCTTTCAC[-/G]GTAACACATTGCCTC | 57630 |
| rs763479706 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244171 | AAGACATTTATTTCA[A/G]TCTGTCTTGCTGTTC | 57630 |
| rs763485182 | snp | C/T | 6.63471e-05 | 0.00575927 | missense | SH3RF1 | GRCh38.p7 | 4:169116463 | CACTGGCTCGACTGA[C/T]ACTGATGGCAGCAGT | 57630 |
| rs763511656 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154950 | AGCTTGGCCACAAGC[C/T]TTCCAAGCAAAGCTG | 57630 |
| rs763568938 | in-del | -/A | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169094253 | ACTGACACAAGGGAC[-/A]ATACAAAGGTTTGAA | 57630 |
| rs763571354 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245241 | ACTGTGAAGTCAGAA[C/G]TGGATGGATGTTGAG | 57630 |
| rs763583898 | in-del | -/TTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231211 | CCCATTATTACATTA[-/TTG]TTGTTCTTACTATAC | 57630 |
| rs763590760 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224614 | TGAACCACCACCACC[A/G]ACCTCTAATTTCTAT | 57630 |
| rs763602973 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098143 | AAATAATACATGCTT[A/T]TTATTGTTTTAAGCC | 57630 |
| rs763626986 | snp | A/G | 1.85046e-05 | 0.00304171 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136670 | TTAAACAATTCCTAA[A/G]AATTCCCTGAGGTTT | 57630 |
| rs763647349 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162663 | AGAAATTAAGACAAA[A/G]CGTTGTTTCTTCATT | 57630 |
| rs763657986 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236697 | CTGTCCCCAGAAATT[C/T]TCATGTAAGCTAACT | 57630 |
| rs763667521 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178462 | ATCAGGACGAGGAAG[A/T]ACATTCAATGCCCAA | 57630 |
| rs763680824 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211235 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 57630 |
| rs763700365 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191541 | AGGAATTAGAAAAAA[A/C]AATTCTATAATTCAT | 57630 |
| rs763710575 | in-del | -/AGTT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144012 | AAAGGTTTAGGTTAG[-/AGTT]AGTTAGGTCTTTGTC | 57630 |
| rs763715207 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121779 | CAACTAGACCTAGAT[A/G]TGATTTGTGAAGAAT | 57630 |
| rs763744865 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131410 | TAGACAGGGACTCAC[C/T]ATGTCACACTTCTTA | 57630 |
| rs763825728 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270555 | AAGCAGCTTTCTAGC[A/C]CAGCCAAGATAAGGC | 57630 |
| rs763830977 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116973 | TGTCTCCCTCTAGTC[C/T]TTTTCCTATTATTCA | 57630 |
| rs763848717 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182397 | GTGTTTCAGCACATA[G/T]ATAATTAAGAATGCC | 57630 |
| rs763855027 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161235 | AAAAGCTTGGCAATT[G/T]AGACAGGCAAACTGT | 57630 |
| rs763898743 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242916 | TCACCCAGCCTGTTA[C/T]AGCAGCACAAATGGA | 57630 |
| rs763901033 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248382 | CTCAGCAAACTAACA[C/T]AGGAACAGAAAACCA | 57630 |
| rs763914450 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153541 | TGCTTTACCACAGCT[-/A]AAGAATGCCCTGTAA | 57630 |
| rs763936146 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169748 | CACTTTTTCTTTTGA[A/G]ACAGGGTCTTACTCT | 57630 |
| rs763937060 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216920 | CTTTGGGAGGCCGAG[A/G]CAGGCGGATCACTTG | 57630 |
| rs763963389 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164682 | TCACTGTGTTCTAGA[C/T]ACTGGAACTAAAACA | 57630 |
| rs763969695 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123101 | CTTTGAACAACTAGA[C/T]GTAAAAACTAAGTCA | 57630 |
| rs763991006 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235727 | ACATAGTTTTGCTCT[C/T]GTTGCCCAAGCTGGA | 57630 |
| rs764001379 | snp | C/T | 8.26207e-05 | 0.00642678 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156662 | TAATGCTTTGGCACA[C/T]GGTAACTGAGGTATA | 57630 |
| rs764011208 | snp | A/G | 1.75265e-05 | 0.00296023 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122281 | TCTAGTATAGGAAAA[A/G]CATAAAGAGAAAGGG | 57630 |
| rs764056140 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202862 | GGTCTTCAATAAAAG[A/C]AACTTTAAAAAACTG | 57630 |
| rs764063936 | snp | C/G/T | 0.000128114 | 0.00800274 | missense | SH3RF1 | GRCh38.p7 | 4:169122197 | CAGCAGCGGCGGTGG[C/G/T]GCCTGGTGGTGTGGA | 57630 |
| rs764067902 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269391 | GCCAAGAATCAAAAA[A/G]TACCCAAAAGTACAC | 57630 |
| rs764068706 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221822 | CTCTGATAGCCTTTT[A/T]TTAGCAGGCTATGTA | 57630 |
| rs764091895 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142699 | GCATCACTAAGTCCA[A/G]TGTTCCTTCCCCAGA | 57630 |
| rs764099420 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225706 | GGATTGGTTATAAAA[A/G]GAAAGTGATAAAAGT | 57630 |
| rs764117103 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179313 | AACATTTTGTCCTTA[C/G]AGCCACCAAAAAGTA | 57630 |
| rs764136235 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208237 | ACCCCAAGTAATAGC[A/C]GTTTCTGTCCAGAGT | 57630 |
| rs764148125 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189129 | AGAAGCTTTTGTAAA[C/T]GTCTAAAATGAAGCA | 57630 |
| rs764157960 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204031 | GCATTCAAAAAATAC[C/T]AGTCGTCTCTCTTCA | 57630 |
| rs764164557 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126798 | GTCTTTCTATGTTGC[C/T]CATGCTGGTCTCGAA | 57630 |
| rs764182100 | snp | C/T | 4.94393e-05 | 0.00497164 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117566 | GACTGTCATTTGCCC[C/T]GTCATGTGCAACAAG | 57630 |
| rs764182106 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263187 | GAACCTTACACGCCA[A/G]GGGAGCATGTCCCAA | 57630 |
| rs764222203 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206492 | AGCCTATGCAACATG[G/T]TGAGACTCCGTCTCC | 57630 |
| rs764232576 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149972 | ACTTCTTATTCTTTG[A/G]AACACAGACATTACC | 57630 |
| rs764235502 | snp | G/T | 1.6557e-05 | 0.00287719 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117494 | TAAGCCCTTTATCCT[G/T]ATATGTTCTGGCCTG | 57630 |
| rs764252748 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113012 | GGGTACAGAGAAAAA[C/T]AGCAGAAGAAATGCA | 57630 |
| rs764322503 | in-del | -/TGTGTGTGTGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187519 | TACAACGAATTTCTG[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57630 |
| rs764328930 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165456 | GGAGGCTAAGGCAGG[C/G]AGATCAATTGAAGCC | 57630 |
| rs764337422 | in-del | -/TACC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199232 | GGACAATTTCAAAGG[-/TACC]TACCCATAAACTAAT | 57630 |
| rs764338994 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268967 | CCCACCAGGACCAGG[C/T]TTCCAAGGCCTCTGT | 57630 |
| rs764343063 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198791 | TAACAAAGAAATAAC[A/T]ATTAGGCTGAAAACA | 57630 |
| rs764359190 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201505 | GAATAATTTAACACT[G/T]ATGTTTCAGGAATGC | 57630 |
| rs764396543 | in-del | -/AAAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258673 | TTTTGAAAAAAACTG[-/AAAT]AATAGAGATTAGTAA | 57630 |
| rs764401221 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102372 | GTGTTCTAGCTTAAT[A/C]CCTGATCAAAGATCA | 57630 |
| rs764405052 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153340 | AAAAAAGCAAAATAC[C/T]TAACACTGATGGAGA | 57630 |
| rs764419899 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161630 | CCTTCATGCATTTCT[C/T]ACTGCTCCATAAAGT | 57630 |
| rs764428245 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239606 | TCTACCTTTAGCAAT[C/G]GTTAGTCCACCTTAT | 57630 |
| rs764431151 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184089 | AGGACTAATGCAAAT[G/T]CACTCACATGAATGC | 57630 |
| rs764443759 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267099 | ACCTATGAAGTTCAA[-/T]TTTTGGGAGCTTAGC | 57630 |
| rs764466527 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101020 | GGAGGCAATTTCATG[C/G]TTGACTAAATCGCAG | 57630 |
| rs764480789 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251170 | ACACAAGTGGACAGA[A/G]GGTTAGTTAGGAGAC | 57630 |
| rs764494765 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154239 | AAAAATATTTCAATA[A/T]ACAGGAACATCTGAA | 57630 |
| rs764558929 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244202 | TCATACATGTTATTT[C/T]TAATTTTCACTACCC | 57630 |
| rs764574910 | snp | A/G | 3.66932e-05 | 0.00428314 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116253 | GCAGAGAAACAGTAA[A/G]TAAGTATGGTCTTAC | 57630 |
| rs764597495 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105406 | TTAAATAATATATTT[C/T]CTTTCCTAACACATT | 57630 |
| rs764668483 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108491 | TCCCCAGTTACCTAA[A/C]GCTGCTCAAGGACAT | 57630 |
| rs764686190 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095870 | AACTAGAAAGAGAGG[A/G]AATCACTAACTTCTC | 57630 |
| rs764708219 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171249 | ATCAGAGAGGATTTC[A/G]GTCCATGAATCCTCT | 57630 |
| rs764717905 | snp | A/G | 4.94385e-05 | 0.0049716 | missense | SH3RF1 | GRCh38.p7 | 4:169120907 | AGCCATCCTGGCAGC[A/G]CTCAAACACTAAAAA | 57630 |
| rs764719724 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102622 | GCAATTTCCTAATTA[-/T]TTTTTTTCTCAATCC | 57630 |
| rs764753992 | snp | A/T | 1.65875e-05 | 0.00287984 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122052 | CTCTGAGGTTTGGAC[A/T]TCGTTTAAATGAACA | 57630 |
| rs764754086 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109497 | TAGGAATCATGGCAG[A/G]GCACAAGGGGTAAGG | 57630 |
| rs764784944 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266134 | TTTTCTCCTTCAAAT[A/T]AGGCAGGAAACACTA | 57630 |
| rs764809074 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248312 | ACCATGCAGCCATAA[A/G]AAAGAATGAGTTCAT | 57630 |
| rs764811639 | snp | A/C | 1.64779e-05 | 0.00287031 | missense | SH3RF1 | GRCh38.p7 | 4:169120919 | AGCGCTCAAACACTA[A/C]AAACATCTCCCCTTT | 57630 |
| rs764811758 | snp | C/T | 1.80494e-05 | 0.00300406 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156358 | CTATGTATCTGGGTA[C/T]AGAGGTAGAGCTGGC | 57630 |
| rs764866631 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188862 | ATGCTCTTCTCTTCT[A/G]TAATATTTTGGTGGT | 57630 |
| rs764921426 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258686 | TGAAATAATAGAGAT[C/T]AGTAAACTAAATGTC | 57630 |
| rs764932279 | snp | C/T | 1.67562e-05 | 0.00289444 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155455 | TGAATATTAACACAG[C/T]TCAAGTTTCTACAGA | 57630 |
| rs764940291 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234295 | GTTAAGTATCCTAGA[A/C]TGCACAAAAGAAACA | 57630 |
| rs764956098 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175863 | TGAAACCCTAACCAG[C/T]GCGAGAGTATTTGGA | 57630 |
| rs764967467 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130582 | CAATACGTTAAATCT[A/G]TGTGAAATTCTTCAG | 57630 |
| rs764984355 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180308 | AAATGCACCCAAACC[A/G]GAGAGTCTGAGGACT | 57630 |
| rs764993295 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113290 | TAATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 57630 |
| rs765026681 | snp | C/T | 1.64822e-05 | 0.00287068 | missense | SH3RF1 | GRCh38.p7 | 4:169096563 | AAAGGCCAGTTTTCC[C/T]ATTACGTTGTAATGT | 57630 |
| rs765029321 | in-del | -/TTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142354 | AAATAATGTTCTAAT[-/TTG]TTATTTATCAGTTTT | 57630 |
| rs765059674 | snp | A/G | | | missense | SH3RF1 | GRCh38.p7 | 4:169269040 | AGCTCCTCGACACCC[A/G]AGCCAACAAGAGTCC | 57630 |
| rs765072566 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181113 | TTAGACATACTATAC[A/G]GTGAGCCGTGCTGAA | 57630 |
| rs765080770 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136737 | TACTTTAAAGTTTGC[C/T]TATGCAGTGTCTGTT | 57630 |
| rs765097794 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144230 | TGCCATTAACTTGCT[C/T]TGTTGACTTGGGCAA | 57630 |
| rs765124632 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135786 | ACCAGTCCAAAGTTG[A/T]AATGAACTAATGAAC | 57630 |
| rs765124771 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101949 | GTATTTTAACTTCCA[C/T]CTGAATGGGCATTTA | 57630 |
| rs765143168 | snp | A/T | 1.87394e-05 | 0.00306094 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116678 | TCAACTATCTAATAG[A/T]TGCTGCTCACCAAAA | 57630 |
| rs765145157 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149480 | TTAAAGAAAAAAAAG[C/G]TACTCAAAGGCAGAT | 57630 |
| rs765146224 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255581 | TAAAACACTACACAC[-/AT]GTGCATATGCATGGA | 57630 |
| rs765147189 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267527 | ACATGTGGGCTCCAA[A/C]TAAGGAAAAGAAAAC | 57630 |
| rs765212763 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215543 | TCTTCCTTCAGTGTT[C/T]GGTAGAATTCATCAC | 57630 |
| rs765225599 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152858 | TGAGGAAGAAAAGGA[-/T]AGTTGAGGACAGGAA | 57630 |
| rs765230079 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232105 | ACAGGAACTGGCTTA[C/G]AGCATTTTAAACACT | 57630 |
| rs765265301 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182038 | TGGAGCTATGCCCAG[A/C]ACATAGTAGGCACTC | 57630 |
| rs765279106 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169140388 | GCAAAATAAATTTGT[A/G]TCCTAAAATACCTTC | 57630 |
| rs765287364 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171042 | CTTATATTTAAGTTT[C/G]ACCTAAAGGTTTCTC | 57630 |
| rs765293170 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219602 | TGTATAAGGAGCAGC[C/T]TGTGTTTGTTCTTCC | 57630 |
| rs765296805 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216590 | TCACCTCTATAGTCC[A/G]AGAACTATGGGAAGC | 57630 |
| rs765325730 | snp | C/T | 1.69513e-05 | 0.00291125 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106930 | TGGAGCGATGGGAAC[C/T]GCGGAGTCCAGGGAA | 57630 |
| rs765344570 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249152 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 57630 |
| rs765374089 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183893 | GACTTTTTATTTCTA[A/T]AAAATCATGAAGTTT | 57630 |
| rs765378724 | snp | C/T | 1.86315e-05 | 0.00305212 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106843 | GGAACGAAGTTGAAC[C/T]TACCTTTCACAAACG | 57630 |
| rs765379308 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159196 | CAACGCTGTGTACTC[C/T]GGTCACATTACATTA | 57630 |
| rs765380245 | snp | A/G | 3.29538e-05 | 0.00405904 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156521 | CTGCACAAAGTTGGT[A/G]GGGAAAAAGCCATGG | 57630 |
| rs765381116 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205220 | CTTTGTTGGCAAGAG[C/G]TGGAAGAAAGTTAAT | 57630 |
| rs765389094 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220678 | CTGTACTGGATTCCT[C/T]TGTCAAACAACTGAC | 57630 |
| rs765412640 | in-del | -/ACTAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191640 | ATTACCTGACTTCAA[-/ACTAT]ACTATACTAAAGCCA | 57630 |
| rs765423349 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172577 | TTATTTGGAGATTAA[A/G]TATGATTTAAGGAGA | 57630 |
| rs765433563 | snp | C/T | 3.29576e-05 | 0.00405928 | missense | SH3RF1 | GRCh38.p7 | 4:169117583 | TCATGTGCAACAAGA[C/T]CTTAGCCTGAGGACT | 57630 |
| rs765477697 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206314 | GATTCATCCCCCTTT[A/G]CAATCATTTAGTGAC | 57630 |
| rs765478308 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176964 | GTAAAGACAGGGTTT[C/T]GCTATGTTGCCCGGG | 57630 |
| rs765486843 | snp | C/T | 1.80677e-05 | 0.00300558 | missense | SH3RF1 | GRCh38.p7 | 4:169136334 | TGAGAAGGGGCACTG[C/T]AGGAGAGCCCAGACA | 57630 |
| rs765490417 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174310 | TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCCAAA | 57630 |
| rs765509124 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210888 | CCGGAGTCTCTCTCA[A/G]CCTATTCTGGCTCAG | 57630 |
| rs765540377 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109243 | TCCATTGATAAATTA[C/T]AATCTCAGCAAGCCA | 57630 |
| rs765541941 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116765 | AATAAAGATGGGATG[C/G]ACGGTGGCCTAAAAG | 57630 |
| rs765553617 | snp | C/T | 1.66857e-05 | 0.00288835 | missense | SH3RF1 | GRCh38.p7 | 4:169136451 | GCCTGGGAGGACTTG[C/T]TGGCCATAGTGAGGG | 57630 |
| rs765596103 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151524 | CTATGGCACCAGTAT[C/G]TGTTTGGGGTACAGC | 57630 |
| rs765626088 | in-del | GAGATGGAGTCTCGCTCTGTCAGGC/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102940 | TTTTTTTTTTTTTTT[GAGATGGAGTCTCGCTCTGTCAGGC/T]TGGATGGAGTGCAGT | 57630 |
| rs765629087 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131205 | CAGCATCATGGCATG[C/T]AATTTATTTTCACAA | 57630 |
| rs765636792 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152598 | CAAAATTAGCCGGAC[A/G]TGGTGGTGCATGTCT | 57630 |
| rs765636854 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163790 | ACCAAAATTCATCGA[A/G]AACAGTCCATTTCTC | 57630 |
| rs765640725 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263160 | ACTCCTTTGTCCGTC[A/C]GTGTTTGTAGTGAAC | 57630 |
| rs765664801 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264137 | CCAAGGGCACAGACT[A/G]GGTGGCTTAAACAAC | 57630 |
| rs765701820 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221184 | AGACGAAAGGCTGAA[C/G]ACAAAACCGCAGGCA | 57630 |
| rs765724944 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153216 | AGTCTAATCTGAGCT[C/G]CAAACCACTATGCAT | 57630 |
| rs765760446 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223164 | GAACATCTATTCATT[A/C]CATTGACAGGTAACA | 57630 |
| rs765769434 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263352 | CCTTACTTGTTGTTT[-/C]TTGTGTGTTACCTCC | 57630 |
| rs765770088 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196508 | TAATTTGAGAACTAG[C/G]ATATTATTAACATAT | 57630 |
| rs765793444 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198649 | TTTACACATGTATAC[A/G]TAAGTATATTAAGCA | 57630 |
| rs765797795 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199833 | GTAACAACATCAAAC[A/G]TTCAGCAAGCACGAC | 57630 |
| rs765812559 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258491 | ATAAAAGTGCTACTA[C/T]AGTACAGTTAAGACA | 57630 |
| rs765815129 | in-del | -/CCTCACTGGGGGGCTCCAGGATTGCACCCGAGG | 1.68028e-05 | 0.00289847 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169156679 | TAACTGAGGTATACC[lengthTooLong]CTTTAAAAAAAAAAG | 57630 |
| rs765819717 | snp | C/T | 1.78918e-05 | 0.00299092 | missense | SH3RF1 | GRCh38.p7 | 4:169116273 | TATGGTCTTACTTTG[C/T]TATCCTTGTCTGGTT | 57630 |
| rs765820909 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135710 | GAATGATTGAATGAA[C/T]GCCCCAGTCATCCCA | 57630 |
| rs765825426 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191705 | TAGCCACATAGACCA[A/G]TGGAACAGAATAGAG | 57630 |
| rs765826109 | in-del | -/TGAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257402 | CAGACAGTCCTGACT[-/TGAG]TACTCCTGTTGACTC | 57630 |
| rs765832640 | snp | A/G | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272095 | TTGCATTTACCATCA[A/G]TTTACAAAAAGTTAT | 57630 |
| rs765838678 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106589 | CAGTTTTTACCTGGA[A/C]ACAATTCAGGCGTGG | 57630 |
| rs765858139 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182707 | TCATAGCAGGCTTTA[C/T]TGCAAGAAAACTTAC | 57630 |
| rs765883624 | snp | A/G | 4.94466e-05 | 0.00497201 | missense | SH3RF1 | GRCh38.p7 | 4:169122118 | CTGGGGCGAGTCTGC[A/G]GCCGTAAATGTGCAA | 57630 |
| rs765884880 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245844 | CAACAGGGGAGTATC[C/T]GTACAAGACCACCTT | 57630 |
| rs765908841 | in-del | -/CAG | 0.00152904 | 0.0276076 | cds-indel | SH3RF1 | GRCh38.p7 | 4:169122173 | GCCTCGGTCCCATTC[-/CAG]CAGCAGCAGCAGCGG | 57630 |
| rs765965887 | snp | A/G | 1.96184e-05 | 0.0031319 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269246 | GAAAAAATCTTCAGA[A/G]ATGTTCATAGTTGTG | 57630 |
| rs765974568 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247082 | AGAGGACTTCAAGGG[C/G]CTATTTAGCAGAGTA | 57630 |
| rs765994151 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201481 | TAACAAAACCAGGGA[A/G]AGTTAAAAGAATAAT | 57630 |
| rs765995906 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234637 | CAGCTTTGGTAGAAA[A/G]TACTGCCTGGCATTG | 57630 |
| rs765996551 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142077 | CCTGCCTCGGCCTCC[C/G]AAAGTGCTGGGATTA | 57630 |
| rs766007723 | snp | G/T | 1.64849e-05 | 0.00287092 | missense | SH3RF1 | GRCh38.p7 | 4:169156490 | GAGGTGGGGGCTGAG[G/T]TAACGGTTTAATAAT | 57630 |
| rs766012189 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233410 | ATTAGAATAAAATAA[C/T]TTAAAACTAAAACTA | 57630 |
| rs766023202 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108309 | TAAGGGACCTGCTGA[A/G]GAATTTTTCTTGGGA | 57630 |
| rs766034339 | snp | A/C/T | 4.95269e-05 | 0.00497608 | missense | SH3RF1 | GRCh38.p7 | 4:169155575 | CAGTCAGAACATCAT[A/C/T]CTGAAGAAACAGCAA | 57630 |
| rs766081100 | snp | A/T | 6.63119e-05 | 0.00575774 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122061 | TTGGACTTCGTTTAA[A/T]TGAACACATAAGCAG | 57630 |
| rs766113353 | snp | A/C | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095605 | GTGTCCTGGGCATGC[A/C]GGTCAGTTGGGGTAA | 57630 |
| rs766114116 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163237 | TATTCAAACACCCAG[-/A]AAAAAAAAAAAAATG | 57630 |
| rs766117654 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208570 | AAGAACATATAATCT[-/A]AAAGGCAATTAGTCA | 57630 |
| rs766122315 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156494 | TGGGGGCTGAGGTAA[C/T]GGTTTAATAATCTGC | 57630 |
| rs766124128 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148304 | TTCCTGGCTCTGTGT[C/G]CCCCTGAGCAAGACA | 57630 |
| rs766151386 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193335 | CTTTTCTCCTCCTTC[A/C]CCCAGGTAAGTTTAG | 57630 |
| rs766166184 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132835 | CAGAGGAGGAGACAA[A/G]ACATCTTGGCTGCTT | 57630 |
| rs766170120 | in-del | -/CC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217014 | AAAAAAAAAAAAAAA[-/CC]AGCCAGGTGTGGTGG | 57630 |
| rs766195750 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185831 | TGAGGCAATGAGATC[C/T]GAGAGGGGGCAGCAA | 57630 |
| rs766207798 | snp | A/G | 1.7098e-05 | 0.00292381 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096737 | AAAGCAGTGATTTTA[A/G]AAAATGGTGTACTGT | 57630 |
| rs766248782 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149292 | ATTTATTAAACAGCC[A/G]TTCCTGGAGCTCAGA | 57630 |
| rs766258224 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252022 | AAAAGATAGGTGGTG[C/T]GCCTACAAGAGCGAG | 57630 |
| rs766260815 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179152 | GGGCAATTAAATCAG[A/G]GAACTATCCCAGATG | 57630 |
| rs766264206 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213993 | TTGTGTAGGCTATTA[C/T]GGGGCTTTTGCCTCT | 57630 |
| rs766278359 | snp | A/C | 1.65979e-05 | 0.00288074 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117483 | TATTAGGCAGGTAAG[A/C]CCTTTATCCTGATAT | 57630 |
| rs766292001 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260047 | ATAAATGGAGTGAGC[A/G]TCTGACCAGAGTGGA | 57630 |
| rs766302232 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134062 | TGGGGTGCCCTCCAA[A/T]GTACACAGTGCCCTA | 57630 |
| rs766309214 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113532 | TTCCAGGAGACACTC[A/G]CTAACAATAAGTCAC | 57630 |
| rs766337609 | snp | A/C | 7.32628e-05 | 0.00605194 | missense | SH3RF1 | GRCh38.p7 | 4:169268825 | GGCTACTTACCCTCA[A/C]TGGGGGGCTCCAGGA | 57630 |
| rs766353644 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188648 | GGAAAAAAGCCCACA[C/T]GTAAAAACATCGACA | 57630 |
| rs766360382 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228937 | AAAAAACAAAAAAAA[A/T]TCTGTTCTTCGAAAA | 57630 |
| rs766370459 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242539 | GGGTCCCAGCTCCAG[G/T]AAATCAAATTCTGTG | 57630 |
| rs766395369 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100965 | ACTCTCTCAAAGCCT[A/G]GCTCCAGTTCTCCCC | 57630 |
| rs766407197 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152967 | AGTTTACCTTCCCTC[C/T]TAATTCCACAGCTCC | 57630 |
| rs766432488 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152378 | TTCTCCCAACCAGAC[C/T]CTCCTCCATTCAAGC | 57630 |
| rs766439634 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182500 | TATGATGAAGGTTTT[C/G]AGGGTATAGAAACTA | 57630 |
| rs766453344 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103835 | ATAAAAATATAAACT[A/T]GGGTAGAAATCTTCT | 57630 |
| rs766492194 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256440 | GTCGTAAAACCAGAA[C/T]TATCTTATGTAGTCA | 57630 |
| rs766525960 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169862 | CCTCCTGAATAGCTC[A/G]GTCCATTGGAAATGA | 57630 |
| rs766549495 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196239 | TCAAGTGTGTGTTTA[C/T]AGTAAGTCCTCACTT | 57630 |
| rs766573781 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156683 | CTGAGGTATACCCTT[C/T]AAAAAAAAAAGAGGG | 57630 |
| rs766585324 | in-del | -/A | 0.163922 | 0.234714 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156683 | TGAGGTATACCCTTT[-/A]AAAAAAAAAAGAGGG | 57630 |
| rs766589443 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144898 | GATTTAGGGAAGAAA[C/T]AATAGAGAAGAAAAT | 57630 |
| rs766598706 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174617 | TTTGCTCTTTTCTAA[-/C]TAAATTTACTCCCAA | 57630 |
| rs766614015 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127664 | CTTAACATGCAGGTT[C/T]TCTTATATAATCCTA | 57630 |
| rs766617048 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137605 | CATCTCGGCATTACA[C/T]ATTGGGCACTTCACA | 57630 |
| rs766644778 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223174 | TCATTCCATTGACAG[A/G]TAACAGACCCTCATC | 57630 |
| rs766656225 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247074 | GCATTAAAAGAGGAC[C/T]TCAAGGGGCTATTTA | 57630 |
| rs766676078 | snp | A/C | 1.71132e-05 | 0.00292511 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120768 | AAAACCATGGAAAAG[A/C]ACAAAGCTTCTCTGT | 57630 |
| rs766681230 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130278 | TTTCTGTTATTTGGG[A/G]AAGGTAGAATCCCTT | 57630 |
| rs766681439 | snp | C/T | 1.66015e-05 | 0.00288105 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117722 | GACCATGGTCACTCC[C/T]CGACTTGTCTGGCCA | 57630 |
| rs766695479 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174286 | AGGCTGCTCTCAAAT[G/T]CTTAAGACTCAAGCA | 57630 |
| rs766707101 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138992 | GGTCTCACTCTGTTG[C/T]CCTGGCTGAAGTGCA | 57630 |
| rs766710154 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161830 | GAAATCATAGTAATA[G/T]AAAGTACCACACAGA | 57630 |
| rs766785039 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175719 | CCACTAGACCATAAG[C/T]TCTAAAAAAACTGTC | 57630 |
| rs766842163 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115462 | TGTGAACTGCACATG[C/T]GAGGGATGTAGGTTG | 57630 |
| rs766842857 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166866 | CACCTCAACCAAAAT[A/T]GGTATCTGCAATGTA | 57630 |
| rs766858564 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098721 | GAAGCATGACACAGC[A/G]GGAGAAACACTGGCC | 57630 |
| rs766880348 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131123 | AGCTCAGAGGTTAGT[C/T]CCCAGAGGACCTAAT | 57630 |
| rs766883911 | snp | A/G | 1.68729e-05 | 0.00290451 | missense | SH3RF1 | GRCh38.p7 | 4:169136551 | CTGCTGCCGAGGAAC[A/G]TTCTCCAGCATCAAC | 57630 |
| rs766932744 | snp | A/G | 1.66043e-05 | 0.00288129 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136459 | GGACTTGTTGGCCAT[A/G]GTGAGGGAAGTGAAG | 57630 |
| rs766948716 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149157 | CTCTCTCAATGTTTT[C/T]CTGATGGAAAGCAAA | 57630 |
| rs767020673 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210459 | ATTACAGTGAAACAT[G/T]ATGCAGATTTTAATC | 57630 |
| rs767045761 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226976 | GTTTGAGACCACCCT[A/G]GTCAACATAACAAGA | 57630 |
| rs767069565 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118711 | ATCCACCCGCCTCAG[C/T]CTCCCAAAGTGCTGG | 57630 |
| rs767073033 | snp | A/T | 1.66214e-05 | 0.00288278 | missense | SH3RF1 | GRCh38.p7 | 4:169116478 | TACTGATGGCAGCAG[A/T]GTGCGTGGCTGAGCC | 57630 |
| rs767076699 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133923 | CTTTGCTGGGCAGGG[A/G]AAAAGGAGAGTCCTG | 57630 |
| rs767078334 | in-del | -/TTTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215658 | TTCACTTCCCTTAGT[-/TTTG]TTTATTATTGAAGTT | 57630 |
| rs767080329 | in-del | -/T | 1.90656e-05 | 0.00308746 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106818 | TTGTTCATTTTTTAG[-/T]TTTTTTCCTGGAACG | 57630 |
| rs767100370 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175457 | TGTTGCTTCTTGACC[-/A]ACTCCAGGCTCTTCC | 57630 |
| rs767162177 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244584 | TCATCTAACTATAAC[A/C]AGCACTGCTTGGCAG | 57630 |
| rs767190038 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199751 | TAAAAAGAAAGACAA[C/T]AAAAGAGAAAGCGAA | 57630 |
| rs767205122 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154342 | TTTTTTATGAAAACG[C/T]TGGCAATCTCACTCT | 57630 |
| rs767250258 | snp | C/T | 3.30715e-05 | 0.00406628 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116416 | GATGCTTGGGGAAGT[C/T]AGTGGAGCAGCTGCT | 57630 |
| rs767250766 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258197 | AGCCAGGACTAGAAA[A/G]CAGGTCTCCTCATTC | 57630 |
| rs767261230 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158357 | GTCAGCACCAGCAAA[C/G]ACCTGGAGGTAAGAA | 57630 |
| rs767301445 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170856 | AAAATGACACAAGGG[A/T]TCAGAGATACGGAAA | 57630 |
| rs767304359 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161066 | CTCATCAGGCCAAGG[C/T]CCCCAAGGATCCACA | 57630 |
| rs767331349 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232441 | TAATGGATATGAAAC[A/G]GAACTTCAAAAAGAT | 57630 |
| rs767334728 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112422 | GGAAAAAGAGGCTGA[C/T]GATAGTCAGGTTTGA | 57630 |
| rs767368058 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124824 | GTTCAAAAGGTAATC[C/T]ACTGTGTATTGTGCT | 57630 |
| rs767377121 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111234 | TGAACCCAGGAGGTA[A/G]AGGCTGCAGTGAGTC | 57630 |
| rs767381577 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192018 | GAACCCAAAAGCAAA[C/T]ACCATAAAAACAAAG | 57630 |
| rs767410849 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138931 | TATATTCTCCATTAA[A/G]ATAAATACACATTGA | 57630 |
| rs767422316 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099851 | AAACCTCTGGGGGGG[C/T]GGGTGGAATGAGAAA | 57630 |
| rs767430368 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209289 | ACAAGACCCTGTCCG[-/A]AAAAAAAAAAAAAAT | 57630 |
| rs767468989 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098288 | TTTCATTTGGTTCTC[A/T]AAGTCAGAAAATGAG | 57630 |
| rs767471487 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248966 | GGCCCAGTGGCTCAC[A/G]CCTATAATCCCAGCA | 57630 |
| rs767507083 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205425 | TAATAAGCATGGCAA[C/T]TCTCCCAAGTGCTAT | 57630 |
| rs767524897 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251347 | ACACATTCCTCTCAG[G/T]GACTTTGTTAGTCAG | 57630 |
| rs767531151 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113964 | AATAAAGAACAACGG[C/T]TGGAAGGTTGAGTTG | 57630 |
| rs767544929 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162449 | GAGAATCCCATAATT[C/T]CACAATAGTCCATCT | 57630 |
| rs767589106 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177482 | AAGCATTGAAATTAT[A/C]CCCACACTGACTTTA | 57630 |
| rs767590700 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240081 | CACAAACACTCCAAC[C/T]GCACACTGGAACATC | 57630 |
| rs767593827 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161716 | GAACAGCTATAAAAT[A/G]TGTATAATTTAATAA | 57630 |
| rs767597543 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216299 | AAAAAATTGGAAATT[-/A]TAATGTTTTAGAAAT | 57630 |
| rs767609440 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237617 | CTGAATCACAGGTAC[A/G]GTAAACAAATCCAGG | 57630 |
| rs767614659 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102062 | TCTAATCGCCCCTGG[A/T]ATAGCCCAAATTGGC | 57630 |
| rs767619111 | snp | A/C/G | 5.80651e-05 | 0.00538792 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169130139 | GGTCACAATTAACCC[A/C/G]GTGGTACTTATATGA | 57630 |
| rs767620675 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135948 | TCACGAGTTTGGACC[A/G]TGGCATCTTAAATCT | 57630 |
| rs767668410 | snp | C/T | 1.64855e-05 | 0.00287097 | missense | SH3RF1 | GRCh38.p7 | 4:169268954 | TGGTCCCACTTCCCC[C/T]ACCAGGACCAGGTTT | 57630 |
| rs767671247 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101302 | AATGAAATTCTGACA[A/C]GTGCTACAACAGGGA | 57630 |
| rs767680650 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241006 | GAGGCTGAGGTGGGC[A/G]GATCACGAGGTCAGG | 57630 |
| rs767711548 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153445 | TTGTCTGGCCCCTGA[A/G]GTGGGGCAAATATGA | 57630 |
| rs767749770 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181418 | CAGGCTCATGCCACC[A/C]TACCCAGCTAATTTT | 57630 |
| rs767756431 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151145 | TCATTCATTCAACCA[A/G]TATTTATTGAAAGCG | 57630 |
| rs767821191 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143010 | CTAAGAGACTGAAGG[C/G]ATTACTCAAGAGTCT | 57630 |
| rs767840134 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172709 | TGGCTGGCAGGGGTG[A/C]GGGTGTTGCCAGAGG | 57630 |
| rs767845303 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250830 | TTTTGGATATGGTGG[A/T]CACAGAAGACCCTTA | 57630 |
| rs767917791 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095032 | GACTACCCAGATCCA[G/T]GACTGCGTGGCACCG | 57630 |
| rs767960282 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169093 | GTTGAGAGTAATACA[G/T]AATATGTGCATATTA | 57630 |
| rs767974345 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099402 | CTCTCTGACACCTTT[A/G]AAAGCAAGACAAATA | 57630 |
| rs767981049 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123845 | TGCAGTGAGCCAAGA[C/T]TGCGCCACTGCACTC | 57630 |
| rs767996282 | snp | A/G | | | downstream-variant-500B | SH3RF1 | GRCh38.p7 | 4:169093874 | ATGGTGAATCTAAAG[A/G]TTTTGTCCCCAAGCC | 57630 |
| rs768000350 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108147 | TGATCCTTTTAAATT[A/G]TTTTACCAAGATGTC | 57630 |
| rs768016676 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169120899 | TTTGAACCAGCCATC[C/T]TGGCAGCGCTCAAAC | 57630 |
| rs768025790 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221200 | ACAAAACCGCAGGCA[A/G]GTCAAGTAGTGATTT | 57630 |
| rs768066283 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171939 | GCACTGCAGTGAATC[A/G]TGTTTATATAATCAT | 57630 |
| rs768073897 | snp | C/T | 6.82745e-05 | 0.00584231 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120780 | AAGAACAAAGCTTCT[C/T]TGTTTAGAACATAGT | 57630 |
| rs768077324 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190483 | CTAGAGGAGATGGAT[-/A]AATTTCTAGAGAGAT | 57630 |
| rs768086260 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221997 | AAAAAACACTACTAA[C/T]AGTTTTTCCTTGAAC | 57630 |
| rs768086359 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095414 | TCTTAACAGGAAATC[G/T]CAATGAAATATACAC | 57630 |
| rs768106116 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158920 | GCTCTCAAAATGCTA[C/T]TGGCAATCATCTTGC | 57630 |
| rs768108061 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172131 | CTGAAATTGATACTG[C/T]ATGAGCCTAAGAAAG | 57630 |
| rs768109024 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207856 | TGCCACTTTCTAAAG[A/G]GTCCTCACAGAAGCA | 57630 |
| rs768115702 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206899 | TAGCACTTTGGGAGG[C/T]AGAACTGGGATCACT | 57630 |
| rs768131754 | snp | A/G | 1.70179e-05 | 0.00291696 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136561 | GGAACATTCTCCAGC[A/G]TCAACTCCTGGCACA | 57630 |
| rs768179906 | in-del | -/CAGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201644 | AGGCAGCTTATTTCC[-/CAGT]CAAAGTTATAATTTT | 57630 |
| rs768189384 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148919 | TAAACTTAACTAGGG[C/T]CCTGGGTACATGTAG | 57630 |
| rs768196065 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159955 | AAATTACAAATTCAC[G/T]GACATGTACCGTTTA | 57630 |
| rs768208394 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152836 | ACAGTCCACAGTCAC[A/G]TGATGTTGAGGAAGA | 57630 |
| rs768221473 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112085 | TACAGAGAAAAGGAG[C/G]GGGCAATAGACACGC | 57630 |
| rs768229315 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263854 | TTTCTGTGCATCTGG[A/T]ATACTGTCACATAAA | 57630 |
| rs768251245 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099375 | ATTATAGACATAAGC[C/T]GCTATGCCCAGCTCT | 57630 |
| rs768290657 | snp | C/T | 3.30147e-05 | 0.00406279 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117514 | GTTCTGGCCTGGGTT[C/T]CTCCTTACCTGTCCT | 57630 |
| rs768319323 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262860 | AAGATCTCATCTCCG[A/C]GTCTCACCATCAAGC | 57630 |
| rs768330220 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230576 | AAATATCACTGATTC[C/T]ACGTGGGCGCAGTGA | 57630 |
| rs768339315 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100826 | CAAAAGTCCCAAACA[C/T]TCCCCTAAGCCTGAA | 57630 |
| rs768349744 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191736 | AACCCAGAAATAAAC[C/T]CAAATCCTTATAGCC | 57630 |
| rs768367136 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268922 | GCTGCTCTGAGACCT[C/T]AATGCATTTGTGCAG | 57630 |
| rs768391157 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238842 | TAGCTCTGTCTTCCA[A/T]CACTTCAAAAGAAGC | 57630 |
| rs768397973 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183322 | GTCTCGCTCTTGTCC[C/G]CAGGCTGGAGTTCAA | 57630 |
| rs768405496 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249770 | CAGATTAAAGTACAG[G/T]AACTGTGAGGCATAT | 57630 |
| rs768415461 | snp | C/T | 1.85792e-05 | 0.00304783 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116635 | GTGCGCTGCAACTAG[C/T]AGATGGGAAGAGGGA | 57630 |
| rs768415507 | snp | A/G | 2.99558e-05 | 0.00387001 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130169 | AACCTGCCGAGAAAA[A/G]AAAAGTTATTAAAAA | 57630 |
| rs768453033 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143677 | AGTAGGACAGGGAGG[A/T]ACACGGACTCCTAAT | 57630 |
| rs768468340 | snp | A/G | 3.42091e-05 | 0.00413562 | missense | SH3RF1 | GRCh38.p7 | 4:169130093 | GGAAAGTAAACGAGG[A/G]GCCAGTTGTCACTGG | 57630 |
| rs768520427 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236739 | TTACTCTGGTCACCA[A/G]TCTCTAACAATCTGA | 57630 |
| rs768557073 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199459 | TGCATCCAGAGAGCA[G/T]AAGTGAAAAGGGGCA | 57630 |
| rs768567785 | in-del | -/GAGGCCGGCGGCATTCTGTACCTG | 1.73444e-05 | 0.00294481 | cds-indel | SH3RF1 | GRCh38.p7 | 4:169116560 | CACAGATGCAGGGCT[-/GAGGCCGGCGGCATTCTGTACCTG]GATGGGTGTCACTGC | 57630 |
| rs768572470 | snp | A/G | 1.67612e-05 | 0.00289488 | missense | SH3RF1 | GRCh38.p7 | 4:169107129 | ACTTCTAGGGTGGGC[A/G]ATGCTGGAGGAGACA | 57630 |
| rs768584485 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197200 | AAAGATGGGGTTTCA[C/T]CATGTTGGCTAGTCC | 57630 |
| rs768586757 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170654 | CACACAGCAAAGAAT[C/G]AGCTCATTAGATGAC | 57630 |
| rs768594737 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138957 | ATTGAGCATCTATTT[C/T]TGGGGGGACTGGGGG | 57630 |
| rs768628454 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239299 | TAAAACATGAAAGAA[A/G]CACTGAAGGCCAAGT | 57630 |
| rs768646657 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184528 | ATTCCTTTCCTTTTG[A/G]GCCAAATTTAACAAT | 57630 |
| rs768675326 | snp | A/G | 4.94711e-05 | 0.00497324 | missense | SH3RF1 | GRCh38.p7 | 4:169120867 | ACCCCTATCTTGCTG[A/G]TATGCATGGATGTCC | 57630 |
| rs768686461 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139947 | TTTAAATGGACAAGT[C/T]TCATTTTTCTATTTG | 57630 |
| rs768732867 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162130 | CCACTGCACTCCAGC[C/G]TGGGCAATAGAGTGA | 57630 |
| rs768743578 | snp | C/T | 1.65726e-05 | 0.00287855 | missense | SH3RF1 | GRCh38.p7 | 4:169116448 | CACAGGCCAGAGGGG[C/T]ACTGGCTCGACTGAT | 57630 |
| rs768744469 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144285 | CCATTTCTCATTTGT[A/G]ACATGAAGCAAGACT | 57630 |
| rs768748849 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201996 | TGGACACAGTATCTA[A/C]TGTTCTCAAGTTTCC | 57630 |
| rs768752625 | snp | A/G | 3.59583e-05 | 0.00424003 | missense | SH3RF1 | GRCh38.p7 | 4:169136425 | TCTCCATGGAGTGGC[A/G]GTTCTGGGATGCCTG | 57630 |
| rs768818446 | snp | A/C/T | 1.64817e-05 | 0.00287064 | missense | SH3RF1 | GRCh38.p7 | 4:169120895 | TCCCTTTGAACCAGC[A/C/T]ATCCTGGCAGCGCTC | 57630 |
| rs768824880 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214534 | AAAAAAACTGACATC[-/T]TGACAATATTGAGCC | 57630 |
| rs768827957 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270708 | CGCTTCCGCAGGTCC[C/T]GATTCCCGGCCCACG | 57630 |
| rs768836172 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146233 | GTTTTATATATATAC[A/T]TTTTTTTTTTTTTTG | 57630 |
| rs768839113 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188716 | ATTTCAACCTGTATA[C/T]GGCAGTTCAATAAAT | 57630 |
| rs768846056 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234313 | CACAAAAGAAACACC[A/C]TCCCCACCCCCCAAA | 57630 |
| rs768905049 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203804 | CCTACAAGATACTAG[A/G]GATCTGTGATTCTAC | 57630 |
| rs768915661 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173924 | ATAAGATCACCCTAC[C/T]CACACACCACCACTA | 57630 |
| rs768926091 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130866 | TCAGGTTGCATAGCA[G/T]GTCCAACTGCAGAAT | 57630 |
| rs768938173 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234971 | ATTACCAAATGTCCC[C/T]TAAGAGGCAAGATCA | 57630 |
| rs768961362 | snp | C/G | 3.31197e-05 | 0.00406925 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116365 | GAGAACGGTCACTAT[C/G]CGGCCACTGGGCTCA | 57630 |
| rs768977759 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115089 | TGTCTCTAAACCCAA[A/C]CATCGGTTATTCTTT | 57630 |
| rs769005234 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175280 | CACCTATTATCCACA[C/G]TCTTGCCTGTTAACC | 57630 |
| rs769014479 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207094 | CTCCCAAATAGCGGG[A/G]CTACAAGTGGGTGCT | 57630 |
| rs769039929 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167467 | GATAAACGAAAACAT[A/C]CATCCACACCCAGAT | 57630 |
| rs769044177 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260513 | AAGCCAGGGATGAAG[C/T]GCTAAAGCCAGAGAG | 57630 |
| rs769064383 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201206 | GAACAATGAAATTTG[A/G]AATTAAAGTTTCTAT | 57630 |
| rs769071721 | in-del | -/GCCAGTACGAGC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232134 | TGGATGGCCAGTGTG[-/GCCAGTACGAGC]GCCAGTACGAGCGCT | 57630 |
| rs769081369 | snp | C/T | 1.71829e-05 | 0.00293106 | missense | SH3RF1 | GRCh38.p7 | 4:169156429 | GGAAGGCAATCTTTG[C/T]CTGCTTCCTTGTCTT | 57630 |
| rs769086281 | snp | A/G | 1.65094e-05 | 0.00287305 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122090 | AGTAACAGACGACAC[A/G]CTCACTTACACACTG | 57630 |
| rs769138730 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265039 | ACAATTCACCCTCAC[A/G]CTAAATGCAGGTCTT | 57630 |
| rs769148863 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155127 | AAAAAATAAACAAAT[A/G]AACTTTTCTCCATCT | 57630 |
| rs769166656 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231477 | AGGCTGAGGCTGGAG[A/T]ATCGCTTGAATCCAG | 57630 |
| rs769170874 | in-del | -/ATGTA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137645 | ATATAAAATAATATC[-/ATGTA]CTATTTTTCCCACTT | 57630 |
| rs769173419 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215932 | CCTCAACCCCCCAAG[C/T]GGCTGGGACCACTGG | 57630 |
| rs769177072 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118884 | GCTCAGGGTTACAGC[C/T]AACTCTAAACATCTA | 57630 |
| rs769206327 | snp | G/T | 1.65485e-05 | 0.00287645 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155617 | ACCTGATCATTAAGC[G/T]GTACCATTAAGCTTG | 57630 |
| rs769209156 | in-del | -/TGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187517 | TTTACAACGAATTTC[-/TGTG]TGTGTGTGTGTGTGT | 57630 |
| rs769240454 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245421 | ATATTTAAATGTCCA[C/T]GTTTCAATTATCCAT | 57630 |
| rs769255113 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183126 | GCCTCGCCAACATGG[C/T]GAAACTCCATCTCTA | 57630 |
| rs769267081 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120423 | GTAAGGTTAATCAGT[A/G]TAATGCATTTATAAA | 57630 |
| rs769288460 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138734 | ATTACTATAGTCTCA[C/T]CATGATCATACCTGG | 57630 |
| rs769311017 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169565 | CTGCACCACTGCACT[C/T]CAGCCTGGGCAACAC | 57630 |
| rs769324625 | snp | G/T | 1.64939e-05 | 0.0028717 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156482 | TTTGCACTGAGGTGG[G/T]GGCTGAGGTAACGGT | 57630 |
| rs769358866 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107876 | CCTTGATTAGACATC[C/T]ATTTTAAGGAAAGCT | 57630 |
| rs769364315 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188696 | GCTTTCTGGCTTATG[-/T]AACAATTTCAACCTG | 57630 |
| rs769379412 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197710 | ACAGAATGATGTAAT[A/C]ACCCTTTCATAAGTA | 57630 |
| rs769412626 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110895 | ATTCTGAAGTTATGC[A/G]TAGAAAATGGAAGCA | 57630 |
| rs769412643 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125683 | GCCTTTCTGGGTCCC[C/T]TGGGCAAATATTATT | 57630 |
| rs769430675 | snp | C/T | 1.75838e-05 | 0.00296506 | missense | SH3RF1 | GRCh38.p7 | 4:169106881 | TAGACTCATTCAAGA[C/T]AGGACCCAGGGAGGA | 57630 |
| rs769437407 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254032 | CAATATCCAATTACA[A/G]TCAAGTTTCATAAGG | 57630 |
| rs769452674 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210114 | ACACGCCATTTTATT[A/G]GTTCTCAAACCTCTA | 57630 |
| rs769476709 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | SH3RF1 | GRCh38.p7 | 4:169117637 | CCACAGCTGCGGGGA[C/T]AACACTGGGACTCCC | 57630 |
| rs769483264 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116186 | AGTGAGTCCTCTCAT[A/T]AGCTAAAAATGACAG | 57630 |
| rs769487195 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242780 | TGCCTGCTCTCTTGC[-/TA]TATATGATGCCTTCT | 57630 |
| rs769496119 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203999 | AAAGCGCCTGGCATA[A/C]TCTTGGCACATCGAA | 57630 |
| rs769498985 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101024 | GCAATTTCATGCTTG[A/G]CTAAATCGCAGAGGC | 57630 |
| rs769500476 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111811 | TCAAACAGGAAAGAA[C/T]TGAGATGAAACATAG | 57630 |
| rs769501810 | snp | A/C | 1.81641e-05 | 0.00301359 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136270 | TGTTTGTAAGTTGAT[A/C]CTTTTGTGGGTGAGC | 57630 |
| rs769553593 | snp | G/T | 3.37445e-05 | 0.00410744 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096717 | GATTTTGGTTAAGGC[G/T]ATTCAAAGCAGTGAT | 57630 |
| rs769565330 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229283 | GTTCTTTTGTCAAAC[C/T]TAACCCAATTCTCCA | 57630 |
| rs769573488 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103490 | TAGATTCTGAAATGT[C/T]TTCTCAATCATACTG | 57630 |
| rs769584468 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205727 | CTTGAAATTTACCAA[C/T]GTACCATACCAACAC | 57630 |
| rs769602185 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118201 | AGCTCCACATCACAC[-/AT]GTGCCCATGTACATG | 57630 |
| rs769615070 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117530 | CTCCTTACCTGTCCT[C/T]ACAGCATTGCGGGCC | 57630 |
| rs769644586 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195918 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 57630 |
| rs769666363 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162389 | AATGACGGCCAAGAC[A/G]AATATTAAAGGTTTT | 57630 |
| rs769666441 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176447 | TTTAGAATATTTTCA[C/T]GGGTGATCAATTTTA | 57630 |
| rs769703453 | snp | A/G | 1.75164e-05 | 0.00295937 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169130112 | AGTTGTCACTGGGCT[A/G]CTTGGGGGCGGGGTC | 57630 |
| rs769751554 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149659 | CACAGTAATTCCCTC[A/T]TCCCAACTTACCCAC | 57630 |
| rs769766108 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106159 | GCTCTGTCACCCAGG[C/T]TGGAGTGCAGCGGCA | 57630 |
| rs769778871 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206465 | ATGGCTTGAAGCCAG[A/G]AGTTTGAAACCAGCC | 57630 |
| rs769781225 | in-del | -/GCAACAAGACCTTA | 1.64798e-05 | 0.00287047 | frameshift-variant | SH3RF1 | GRCh38.p7 | 4:169117574 | TTTGCCCCGTCATGT[-/GCAACAAGACCTTA]GCCTGAGGACTTGTC | 57630 |
| rs769782965 | snp | A/G | 3.46554e-05 | 0.00416251 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117809 | CAAACATAGATGGAA[A/G]GCCCAGTCCATCAGC | 57630 |
| rs769803170 | snp | G/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271343 | GGACGCCTTCTCCCT[G/T]AGGAGAACGCGCCTG | 57630 |
| rs769812884 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104476 | TTACTAAGAGCACAA[C/T]AGATGAGAGGAAAGA | 57630 |
| rs769888472 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214371 | AGTACAGCCTGCAGG[A/G]CTGTGAGCCAATTAA | 57630 |
| rs769895141 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207670 | GTTCTGGATGCTTCG[A/G]GCTTTGCTATGAAGA | 57630 |
| rs769937357 | snp | A/G | 3.62996e-05 | 0.0042601 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136643 | AGCAACCAACAAACC[A/G]ACACAAGAAGGTTAA | 57630 |
| rs769992039 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245027 | GTAAGCGGATATTCC[A/G]TCTTAATGATAGTAG | 57630 |
| rs769993267 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155950 | AAATGTACATCCTAC[C/T]GCTTTTCTCCACAAA | 57630 |
| rs770005137 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107706 | TTAAATGTAAACCTG[A/T]CAGCACTCTATTCCA | 57630 |
| rs770018217 | snp | A/G | 1.67947e-05 | 0.00289777 | missense | SH3RF1 | GRCh38.p7 | 4:169116528 | TGTGGGGAGGCCAGC[A/G]AGTGATGGGACAGGC | 57630 |
| rs770059888 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177040 | TCTTTAGGAGGCTGG[C/G]ATTTTGGTGCTGGGA | 57630 |
| rs770085298 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246548 | GGCAGGCCTGAGGGT[A/G]TGACTGTCTATTTAA | 57630 |
| rs770106498 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198443 | ACTTTAAAATATACA[-/C]CATTTGTGAATGTCC | 57630 |
| rs770126056 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270237 | CCAGGGCTGCACCCC[C/T]GCTCCCACGGCGCCA | 57630 |
| rs770139850 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159670 | TACATGTGTGAACCA[C/T]CATCATTGTCATCAT | 57630 |
| rs770144567 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186514 | GTGCAAAAAATAGAA[C/T]TACACTATTATAAAA | 57630 |
| rs770154376 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191513 | CCCATCAAAATACCA[C/T]CATTATTCTTTGAGG | 57630 |
| rs770164041 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100541 | GAGACAGGGTTTCAA[C/T]ATATTGGCCAGGCTG | 57630 |
| rs770201189 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211284 | TCAGGAGATCGAGAC[C/T]ATCCTGGCTAACACA | 57630 |
| rs770203470 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098920 | CCCATTATGATCATA[C/T]GGCTTAGACAAGAGT | 57630 |
| rs770208802 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179619 | CTTCAGGTTATATAC[A/G]GATAACTTCAGTAGA | 57630 |
| rs770220473 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226603 | CCCTAGAAAGGGAGA[C/T]ACAGAAAGGCACACA | 57630 |
| rs770227271 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213006 | TATAAATATCCATGT[C/G]CAGGTTTTTGTAAAG | 57630 |
| rs770254198 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178020 | CTGAGGTGAGTGGAT[C/T]GTTTGGGGTGAGGAG | 57630 |
| rs770284095 | snp | C/T | 1.72285e-05 | 0.00293495 | missense | SH3RF1 | GRCh38.p7 | 4:169122185 | TTCCAGCAGCAGCAG[C/T]AGCGGCGGTGGCGCC | 57630 |
| rs770292333 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165069 | AGAGAGCAGGAATAT[G/T]TACTGGGAAGATTCT | 57630 |
| rs770298722 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169171171 | CAAACTGGGTTCAAA[C/T]GAGGCAAACACCACG | 57630 |
| rs770303758 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148769 | GTTGCATACGAAAAT[C/T]AGGGAAGAAAGGCTT | 57630 |
| rs770333018 | snp | C/T | 4.94409e-05 | 0.00497172 | missense | SH3RF1 | GRCh38.p7 | 4:169156582 | TCATCCACTTGTCTT[C/T]GCAAAATGATGATGT | 57630 |
| rs770374469 | snp | A/G | 1.77941e-05 | 0.00298274 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156719 | TTTTAATAAAATAAT[A/G]GTCTTAAAATGTCTC | 57630 |
| rs770379881 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104680 | GCCGAGGCAGGTGAA[G/T]TGCCTGAGCTCAGGA | 57630 |
| rs770393643 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133615 | AAACCCCATCTCTAC[C/T]AAAAATATAAAAACT | 57630 |
| rs770394903 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182063 | GCACTCAATTTTTGT[C/T]GCAGAAATAAATGGA | 57630 |
| rs770425718 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216535 | GCACATAAATGTCTG[G/T]TCAGAAATAAGAAAT | 57630 |
| rs770428169 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202821 | AAAGTAAAGCTTAAT[A/G]AATTTACCATTATAA | 57630 |
| rs770434207 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180987 | TCTCTTTACTCACAA[A/C]TTCGCTCTAGGGACC | 57630 |
| rs770450781 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257926 | GCACAGTGTGGGCTT[C/G]TAAGGGAACATTAAA | 57630 |
| rs770482758 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169217 | TTACTTTGAAATAAA[C/T]TTATTACAAGGATAT | 57630 |
| rs770486672 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251078 | GCGACTGAAGTCTAA[C/T]GGACCATTATATAAC | 57630 |
| rs770515514 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202434 | TCTGTGGATGAGAAA[C/T]GAAGTCCAGGCTGGG | 57630 |
| rs770523924 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252145 | CTGCGTTTTCACATT[A/T]TATAGCATGTTGAGT | 57630 |
| rs770537365 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122412 | GGCAGAATCAGCAGG[C/T]TAACTGATATGAAAG | 57630 |
| rs770537490 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138462 | TGTCTTCTTCCACCA[C/T]AAGCTTATTTAGACA | 57630 |
| rs770550740 | snp | A/G | 3.29669e-05 | 0.00405984 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156608 | GATGTCACCTTTGCT[A/G]AATTTAAGGTCTCCA | 57630 |
| rs770551654 | in-del | -/ACA/ACACTGGGGCGAGTCTGCGGCCGTAAATGTG/ACACTGGGGCGAGTCTGCGGCCGTAAATGTGCAAT/ACACTGGGGCGAGTCTGCGGCCGTAAATGTGCAATCTGGT | 9.90525e-05 | 0.00703698 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169120989 | TATATAGCAACATAC[lengthTooLong]CTAGAATAGAAAATA | 57630 |
| rs770553345 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229070 | AGGAAAGAGCTCTTT[C/T]AGTTTACAGGGTTTG | 57630 |
| rs770575775 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103295 | GGAAATTTTATGCTT[A/G]TTCTCATTATAATCT | 57630 |
| rs770591137 | snp | A/G | 1.70339e-05 | 0.00291833 | missense | SH3RF1 | GRCh38.p7 | 4:169106916 | GCCTGGCGAGGAGGT[A/G]GAGCGATGGGAACTG | 57630 |
| rs770595080 | in-del | -/TT | 1.82241e-05 | 0.00301856 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136655 | ACCAACACAAGAAGG[-/TT]AAACAATTCCTAAGA | 57630 |
| rs770595637 | snp | G/T | 1.68111e-05 | 0.00289918 | missense | SH3RF1 | GRCh38.p7 | 4:169106997 | GCTCCTGCCACTGCA[G/T]TCGTGACCGGTCCGT | 57630 |
| rs770611960 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266120 | ATCCCACACTCTCCT[C/T]TTCTCCTTCAAATTA | 57630 |
| rs770613716 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222459 | GACAGAGCTGAGACT[C/T]GGTCTAAAAAATACA | 57630 |
| rs770618984 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248033 | AAATGCTTTTACACT[C/G]TTGGTGGGACTGTAA | 57630 |
| rs770641355 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230099 | TAATCCCAGCTACTC[A/G]GGAGGCCGAGGCAGG | 57630 |
| rs770642879 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217693 | ATTGGCCTGGGAGAA[C/G]GGAATAGGGAGTTAC | 57630 |
| rs770646466 | snp | C/T | 1.64852e-05 | 0.00287094 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117656 | ACTGGGACTCCCAGC[C/T]ACGCCATTTCCCTGG | 57630 |
| rs770664355 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262375 | CTCATTTTAAAAATG[A/G]TAACACTTAGGCTGG | 57630 |
| rs770677923 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147790 | CATTTATATGCCACA[C/T]ATGCACACACATGCT | 57630 |
| rs770685609 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181584 | CCTTTTAAGTCCTCA[-/C]TCCTGAAGGTTAATA | 57630 |
| rs770702379 | in-del | -/CAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230855 | AGTGAGAAACCACCT[-/CAA]AAAAAAAAAAAAAAA | 57630 |
| rs770712982 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166169 | CACAGATTGGGAAAT[-/AT]ATATATATATATAAT | 57630 |
| rs770753957 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260954 | TAAATATACAGCTAA[A/G]GATCCCTAGAGAGGT | 57630 |
| rs770780723 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209008 | AAAATGAGGCAGTAG[C/G]ACAGGGCGTGGTGGC | 57630 |
| rs770798700 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173652 | ATGTTAGCTCTGGAG[A/C]AAACAATAAAAGCCT | 57630 |
| rs770808813 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121380 | CCCCAAATGAGAACA[C/T]ATGGTATGAAATCCC | 57630 |
| rs770824323 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220247 | TTCCTTCTTTTCTAT[A/G]AACTTCTTTTAATCA | 57630 |
| rs770866867 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163699 | GATTGTCTGTTCCAC[C/T]TCATATTTTCCACCC | 57630 |
| rs770870559 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209874 | GGCTCACTGCAGCCT[C/T]GACCTCTCAGGCTCA | 57630 |
| rs770900780 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175127 | CATTCTTTCACATTG[C/T]ACATCCACTTAATGC | 57630 |
| rs770926301 | snp | C/T | 1.68975e-05 | 0.00290662 | missense | SH3RF1 | GRCh38.p7 | 4:169107147 | GCTGGAGGAGACACG[C/T]GGGGCTTCCGTTTAG | 57630 |
| rs770935736 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261072 | AAGTCAAAGATGGAC[C/G]AAACTCAGCCCCCTC | 57630 |
| rs770941844 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239213 | CTGCCAAGATTGTGC[C/T]GACAAGACTGGTTAT | 57630 |
| rs770948336 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177954 | GCAAGATCCTTGAGA[C/G]TAAAAAAGAACTTTT | 57630 |
| rs770970560 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240384 | TTAATTTTTTGCAGA[-/G]ATGGGATTTCACCAC | 57630 |
| rs771002586 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112573 | CATACAATTGCAAAT[C/T]ATCCCTGCAGATGAA | 57630 |
| rs771024806 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226376 | TTCATCACAGTTGTC[A/G]TGTCTACATATCAAG | 57630 |
| rs771056188 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101868 | TTTTGGTGATAACTG[C/T]CAAGGTACAATTCAA | 57630 |
| rs771070152 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236173 | CTCTCCCTCTAGACA[A/C]ATGGCAGGACTGCCC | 57630 |
| rs771073485 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114510 | GGTGGACATCCTTGG[C/G]GAGTCACTATTCTGT | 57630 |
| rs771097950 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245005 | ACAGTACATATACTC[A/G]TATTCTGTAAGCGGA | 57630 |
| rs771118198 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104763 | AAAAAAATTAGCCGG[A/G]CGTGGTGTGTGCCTG | 57630 |
| rs771133395 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243973 | GAGTTGCCAAAGTCA[A/G]TATGTGAAGTCTGTC | 57630 |
| rs771152052 | snp | A/T | 1.6516e-05 | 0.00287362 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120992 | TATAGCAACATACCT[A/T]GAATAGAAAATAATA | 57630 |
| rs771197345 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198442 | ATACTTTAAAATATA[C/T]ACATTTGTGAATGTC | 57630 |
| rs771276794 | snp | A/C | 1.64838e-05 | 0.00287083 | missense | SH3RF1 | GRCh38.p7 | 4:169120891 | GATGTCCCTTTGAAC[A/C]AGCCATCCTGGCAGC | 57630 |
| rs771278785 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213648 | GTTTCATAGTTTTGT[A/G]TTTTACATTTAGATC | 57630 |
| rs771289034 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199559 | CACTGGTTAGATCTC[A/C]GTCACACAGTATGTA | 57630 |
| rs771298703 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203746 | ACTGTGAAACGAATG[A/C]CTGAATAATCTCCGT | 57630 |
| rs771305767 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250346 | GCTTGCGGCAAGATT[-/A]TTTTTTAAATCATTC | 57630 |
| rs771329778 | snp | C/T | 1.8179e-05 | 0.00301483 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136647 | ACCAACAAACCAACA[C/T]AAGAAGGTTAAACAA | 57630 |
| rs771352149 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146562 | AGAATAGTGGTAGAT[A/G]TTATTGAGAGGACAA | 57630 |
| rs771360517 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157810 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT | 57630 |
| rs771374215 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225087 | GAGAGCAAAGCTCTG[C/T]ATTGATGAATTCAAA | 57630 |
| rs771379920 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098720 | GGAAGCATGACACAG[C/T]GGGAGAAACACTGGC | 57630 |
| rs771408763 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202736 | GAAATAGCTTATGAC[-/A]AAAAGAAAACCTAAC | 57630 |
| rs771417625 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097895 | GCTGCCATGTTGTGA[A/G]GACACTCAACATCTC | 57630 |
| rs771441376 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150518 | AAATCCACTCTCAGC[A/G]TTTTTCAAGAATACA | 57630 |
| rs771446270 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131108 | GTCAGGACAAAGAAA[A/G]GCTCAGAGGTTAGTT | 57630 |
| rs771450473 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158608 | GTAGTGTGGAAAATG[A/G]ACGTGAAGTGGGCAG | 57630 |
| rs771455848 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208712 | TGGCATCAAACATCT[A/T]GTCTGAAGCTGCATC | 57630 |
| rs771461693 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121428 | GCTGGCTTCTACACA[-/C]AAGCTGAACCTAGAG | 57630 |
| rs771466380 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256092 | TTTAAAAATTAGGAC[C/T]GCACTACAAAGCACA | 57630 |
| rs771467337 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253291 | ATGTTAGGTAGACCT[A/C]GTGTTACTTATTTGT | 57630 |
| rs771469550 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225040 | ACCAGCTCAGACAGA[C/G]AGAGACCAATTACCA | 57630 |
| rs771492694 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173816 | CATGTCTTAGAACCT[C/T]GGTTATGAAAACTTC | 57630 |
| rs771510213 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161132 | ACACATGAAAGGGAT[A/G]CTTAAAAGGAGAGAA | 57630 |
| rs771566166 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227883 | TTGCATTTTTCAATT[C/G]AGGAAGAGAAATTTT | 57630 |
| rs771574312 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101635 | CAATTTAAAAAATAA[C/G]ATATATGAATGAATA | 57630 |
| rs771581892 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206743 | ACACAAGCCATGGGA[A/G]ACATAAGAAAATGAC | 57630 |
| rs771596752 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135124 | ATGTTCACTTGAGGC[C/T]AAGAGCTTGTTACCA | 57630 |
| rs771615026 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263952 | GAGTAGGGAGGGGCT[C/G]AACAACTTCTCAAAG | 57630 |
| rs771625845 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100876 | CTTTACTTCCCCCAC[A/G]CCACACCTTGGCTCA | 57630 |
| rs771634079 | snp | C/T | 1.74656e-05 | 0.00295508 | missense | SH3RF1 | GRCh38.p7 | 4:169116564 | GATGCAGGGCTGAGG[C/T]CGGCGGCATTCTGTA | 57630 |
| rs771649990 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215120 | TTTTTTCTTATCAAG[C/T]TGAGGTAGTCCCCTC | 57630 |
| rs771654321 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264796 | CCTTCTACATTATCA[A/G]ATTTGAGGCCTCATC | 57630 |
| rs771680542 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120737 | ATTATAATGTGAAAG[C/G]AATCTGGATAGGCTG | 57630 |
| rs771693082 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154758 | CCTTCTTTGAAAATG[C/G]CTTCGATTTTATTTT | 57630 |
| rs771702267 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239104 | ACTAGACATATCTGG[C/G]TCATTTAAGTCATTC | 57630 |
| rs771710345 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114386 | TTACACTGGGCCCAC[C/G]TGGATAATTCAGGCT | 57630 |
| rs771719169 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193193 | GCTCAGTGCATACTG[C/T]CCAAGTGATGGGTGT | 57630 |
| rs771719595 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184670 | GGCTGGTAGAGAAAA[A/G]ATTCCTGACTTCCTA | 57630 |
| rs771752763 | snp | C/G/T | 0.000155005 | 0.00880242 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122273 | ATTCAAAGTCTAGTA[C/G/T]AGGAAAAACATAAAG | 57630 |
| rs771772514 | in-del | -/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222789 | TCTATTTTGTGACAC[-/TT]TAACTTTAATGGAAC | 57630 |
| rs771781742 | snp | G/T | 9.96198e-05 | 0.00705691 | missense | SH3RF1 | GRCh38.p7 | 4:169268897 | CTTTTGAGCTACAAT[G/T]AGCCACAGTGCTGCT | 57630 |
| rs771810098 | in-del | -/GAAGAAACA | 1.65089e-05 | 0.00287301 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155578 | TCAGAACATCATCCT[-/GAAGAAACA]GCAAATCATTAATCT | 57630 |
| rs771816922 | snp | A/C | 1.67337e-05 | 0.00289251 | missense | SH3RF1 | GRCh38.p7 | 4:169107105 | GGAAGCTCTGCACTG[A/C]CCAGCTCCACTTCTA | 57630 |
| rs771819975 | snp | C/T | 5.44311e-05 | 0.00521657 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136294 | GGTGAGCTCTTTTTA[C/T]ATAACACTTGTTTGA | 57630 |
| rs771837393 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220417 | AAAAATGAAAGAACC[A/G]AATGAACTTCTGTTT | 57630 |
| rs771839610 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233014 | AGAACTTTGGGAGGC[C/T]GAGGCAGGCAGATCA | 57630 |
| rs771887806 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245339 | ATCTATGGAGAAAAC[A/G]TGAAATTTTGAGTAA | 57630 |
| rs771902348 | snp | A/T | 5.66171e-05 | 0.00532028 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268775 | AAAGAAAAAATGTGG[A/T]CATTACCACCTTTAT | 57630 |
| rs771908597 | in-del | -/AG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263286 | AACCCCATCATAGAT[-/AG]AGACTTATTCTATAT | 57630 |
| rs771927474 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221349 | ACAAACTGTGATAGA[C/T]GATCAACCAGCTGAG | 57630 |
| rs771945414 | snp | G/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096069 | TGCATTCACTCTATG[G/T]CAAAACGAATCTCTT | 57630 |
| rs771948625 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186210 | GTATGGTAGCTTTAA[A/G]GAGAGTGGTAGCTGG | 57630 |
| rs771964221 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164367 | GAAAAGCAACTAAAA[A/G]GATGATTCTACTGAC | 57630 |
| rs771982336 | snp | A/C | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271885 | AAGCACGCTGAGAGG[A/C]GCCTCTTTTATCTGA | 57630 |
| rs771983705 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268090 | ATATTTCTAATAAAT[A/G]CAGAAATTTTGTGTG | 57630 |
| rs771989389 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146474 | AACTTGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 57630 |
| rs772007794 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175657 | CTTTCTACCCTGCTC[A/G]TTTTCTTCATGACAT | 57630 |
| rs772016567 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181157 | CTGTGTAATTTATCC[-/T]GTTTTTCTCCTCCCT | 57630 |
| rs772027196 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126190 | ATTGGTGGCACCTAG[C/T]TTTGCAGCTAGAAGA | 57630 |
| rs772046056 | snp | C/T | 1.6492e-05 | 0.00287154 | missense | SH3RF1 | GRCh38.p7 | 4:169117667 | CAGCCACGCCATTTC[C/T]CTGGAGCTTCTGGGC | 57630 |
| rs772065376 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207222 | CTCAGCCTCCCAACA[A/G]GCTGGGATAATAAGA | 57630 |
| rs772096794 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189725 | TTAGCTGCGTGCTCT[C/T]GGGCAAGTTGCTCGA | 57630 |
| rs772115042 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127840 | ATTAAGCCAGCCTTA[C/T]GTCTTTTCCCACTAC | 57630 |
| rs772170763 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130984 | CAATGTGGTTGGCTG[A/G]TACCTGCCTCCCTAA | 57630 |
| rs772227080 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184330 | CCAGAGCACATCACA[C/T]GTGCACACATCCAAA | 57630 |
| rs772228651 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147499 | GGGGGAATGGTGATC[A/G]CCAAGAAAGAATCTG | 57630 |
| rs772252757 | in-del | -/ACAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139328 | GCCCTTAAGGACCTT[-/ACAA]ACAGGCATAAAAATA | 57630 |
| rs772264514 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132001 | GGGCCTGAGAAGACT[C/T]GGTATCCAGGGCCCT | 57630 |
| rs772279261 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255440 | TATGAGCTATTAAAA[A/G]ATAACCAAAACATGG | 57630 |
| rs772280831 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260785 | TTGCCAAAGAGATCT[A/G]CATCAGGCTACTTTT | 57630 |
| rs772290926 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097752 | GTCTCCTCCTATGAT[A/G]CACAGGATGACCTGT | 57630 |
| rs772348470 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117250 | TTGAGATCATATGAT[C/T]TCAACTATAGAAGTC | 57630 |
| rs772350009 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224971 | AAGGGTTTTATACTT[C/T]AAGCAGAGTAATCCA | 57630 |
| rs772352095 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210381 | GCTCATACTCCAGAT[A/G]TGCTTTAACCTATGA | 57630 |
| rs772363851 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196080 | TTGGCCTCCCAAAGT[A/G]TTGAGATTACAGGAG | 57630 |
| rs772391891 | in-del | -/GTGGTCT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157338 | TAAGTGTATAGACAC[-/GTGGTCT]TTTACAGCCTAAGAT | 57630 |
| rs772395673 | snp | A/T | 9.11353e-05 | 0.00674977 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136655 | ACCAACACAAGAAGG[A/T]TAAACAATTCCTAAG | 57630 |
| rs772410386 | snp | C/G | 1.91503e-05 | 0.00309431 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107246 | AGTTGGAGAATGACA[C/G]TACTATTGCTGGTGT | 57630 |
| rs772442969 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211678 | TCATAATTAAAAGGG[A/G]GGAAGTGTTATGAAC | 57630 |
| rs772444332 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157531 | TATGATACTTTTCAA[C/T]GGCATTGGGGGTGCC | 57630 |
| rs772460543 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228114 | GCAGACCATCATTGA[A/G]TAGAATATATATTAA | 57630 |
| rs772485967 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246944 | TAAAAGAGGAAGGGG[A/G]AAGCAATAAAGTTCC | 57630 |
| rs772488469 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202273 | GTTTCTTTATCCTGA[C/T]GCTTCAGTTTAATGT | 57630 |
| rs772492833 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235247 | GCTTACATAACAACA[C/T]AGTGATATCCTTACA | 57630 |
| rs772495249 | snp | A/G | 1.85393e-05 | 0.00304455 | missense | SH3RF1 | GRCh38.p7 | 4:169116630 | TGGTTGTGCGCTGCA[A/G]CTAGTAGATGGGAAG | 57630 |
| rs772512348 | snp | C/T | 1.65181e-05 | 0.00287381 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155585 | ATCATCCTGAAGAAA[C/T]AGCAAATCATTAATC | 57630 |
| rs772514221 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167667 | CAAAAACAGGTGAAA[C/T]GAATCTCTTGTGGTA | 57630 |
| rs772520714 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259671 | AAAAGCTTTGGGAGG[C/G]TGAGGGAGTTGAAGT | 57630 |
| rs772555727 | snp | A/T | 0.000102354 | 0.00715308 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096489 | CTTTGTTGTGTGAAG[A/T]GATTTTAAGCTTCTT | 57630 |
| rs772556665 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100912 | TTCCTTCTAGTGGGA[A/G]TCTCCTTTGACGCTA | 57630 |
| rs772584656 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188752 | ATGAAAAGCTTTATG[C/T]AGAAGTGGCCAAAAT | 57630 |
| rs772604175 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169142 | GGAGCATTCTTCTAG[C/T]CAATTAAATGTGAAG | 57630 |
| rs772621109 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230075 | GCCAGGCGTGGTGGT[G/T]CATGCCTGTAATCCC | 57630 |
| rs772622396 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160455 | CAGTGATATACATTA[C/T]GGTTAGCCTAGGGTT | 57630 |
| rs772629019 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144537 | AGGGAAACAGAGACA[C/T]ATCTTTTCTGACTCA | 57630 |
| rs772636183 | snp | A/G | 3.29821e-05 | 0.00406078 | missense | SH3RF1 | GRCh38.p7 | 4:169156484 | TGCACTGAGGTGGGG[A/G]CTGAGGTAACGGTTT | 57630 |
| rs772649550 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105012 | GTTAAAAAGTGTGCC[-/A]AAAAATATGAATGCA | 57630 |
| rs772659363 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109126 | TCCAGTAGCTTCCAC[C/T]TCTAAGGTAGCAGTC | 57630 |
| rs772690674 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150561 | TATTAACTATAGTCA[C/T]CCTATAGAACTCTTG | 57630 |
| rs772701341 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264896 | TTCCTGTTTAGGTCA[A/G]CCCCTTTGAAATATT | 57630 |
| rs772711041 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098574 | GCACAGGGACCAAAT[C/T]ACTACCCAAGATCTG | 57630 |
| rs772721902 | in-del | -/CTTA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263338 | TTCACTATCTGCTGC[-/CTTA]CTTGTTGTTTCTTGT | 57630 |
| rs772745074 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097108 | CAGGGGGGGTTCAGT[C/T]CTCTCTGAACCGCCT | 57630 |
| rs772766033 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269340 | AGGGGGAAAAGAGAA[C/G]ATGAGTGTTGTTATC | 57630 |
| rs772767728 | snp | G/T | 1.64819e-05 | 0.00287066 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156593 | TCTTCGCAAAATGAT[G/T]ATGTCACCTTTGCTG | 57630 |
| rs772771964 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194155 | TAGTCGTCATCTAAA[A/C]ATTTTTCTAGACAGT | 57630 |
| rs772779731 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239187 | TTTTCACAATATGTG[C/G]ATAGCCATTTCTGCC | 57630 |
| rs772780653 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135299 | AAACTTTTTGAGGAC[A/C]AGGACTGGTATTTCT | 57630 |
| rs772805045 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239904 | TGGTGTGCACTTATA[C/T]TCCCAGCTACTTGGG | 57630 |
| rs772827031 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101750 | CACCCCTTGTTCCCT[A/T]TGAACAAAGCGCTGT | 57630 |
| rs772844264 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256295 | AGGGAGGAAGAAAGG[A/G]AGGAAGGGAAGGAGG | 57630 |
| rs772872703 | snp | G/T | 1.80465e-05 | 0.00300382 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156364 | ATCTGGGTACAGAGG[G/T]AGAGCTGGCAAACAG | 57630 |
| rs772884715 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215129 | ATCAAGTTGAGGTAG[A/T]CCCCTCTATTGCTAG | 57630 |
| rs772904626 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201277 | GCTTTAACAATTGAC[A/G]AATACTTATTCTGCA | 57630 |
| rs772939726 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166583 | AATGGTGGTAACCTA[A/G]GTGGTTAAACTTCAC | 57630 |
| rs772987094 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207381 | ACAGTGAGCCATGAT[C/T]GTGCCACTGTGCTCC | 57630 |
| rs772988324 | in-del | -/TTGTGACTGGTGCCACATAAT | 1.70983e-05 | 0.00292384 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169117783 | CATTTGTCACCGCCC[-/TTGTGACTGGTGCCACATAAT]TGCCAAGACACAAAC | 57630 |
| rs773006724 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221548 | AGTTTGAAAACATTA[A/T]CATTGGAAAAGAAAG | 57630 |
| rs773009655 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212890 | CTTCTGGCAACCACT[A/G]ATCTTTTTACTGTCT | 57630 |
| rs773029534 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167760 | TCTGAGACTATAAAT[A/G]TATTCTGTATCTTGA | 57630 |
| rs773046877 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172283 | TCAATACTGGCTAAA[A/C]CCATGTGTCCAGTTA | 57630 |
| rs773062440 | snp | A/G | 3.38398e-05 | 0.00411324 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096722 | TGGTTAAGGCGATTC[A/G]AAGCAGTGATTTTAA | 57630 |
| rs773069499 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206258 | ATATCTTAGCATGCC[A/G]CACATGATTCAATCT | 57630 |
| rs773081933 | in-del | -/AG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159377 | CACAGCAATCGACAG[-/AG]AGAGAGAGAGATAGA | 57630 |
| rs773130972 | in-del | AGTTG/GTGTGTGTGTAGTTGACAA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187558 | TGTGTGTGTGTGTGT[AGTTG/GTGTGTGTGTAGTTGACAA]GCAACTTTTTAAGCT | 57630 |
| rs773146681 | snp | G/T | 1.64887e-05 | 0.00287125 | missense | SH3RF1 | GRCh38.p7 | 4:169120871 | CTATCTTGCTGGTAT[G/T]CATGGATGTCCCTTT | 57630 |
| rs773148901 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176636 | ACCTCAGTTTCCCAC[A/G]TTCAAGCGATTCTCC | 57630 |
| rs773149462 | snp | A/G | 1.69743e-05 | 0.00291322 | missense | SH3RF1 | GRCh38.p7 | 4:169269161 | CAGAAGCATCAAGGC[A/G]CTCTAGACACACCGG | 57630 |
| rs773159698 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216741 | CTTCAGTATTTTTCC[-/T]TCTATTTATATTTTT | 57630 |
| rs773165395 | snp | A/G | 3.63055e-05 | 0.00426045 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136282 | GATCCTTTTGTGGGT[A/G]AGCTCTTTTTATATA | 57630 |
| rs773166248 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169149184 | CAAAAAGAAACTCTT[A/C]AATTAGAAAGAAGCC | 57630 |
| rs773176300 | snp | C/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272011 | ATAGGTTTTGAGGTT[C/T]TTCAGTCTCGATTTA | 57630 |
| rs773182872 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112467 | AAGAACTGATTTTTA[A/G]ATGTTCAAAGAAAAT | 57630 |
| rs773189311 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138257 | TGGCCTGAACCTCAC[C/T]GTAGAGCTCTAATAA | 57630 |
| rs773190633 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217554 | AAGTACTAGAGACAG[-/A]AAGAAAAGCCTAAAC | 57630 |
| rs773205387 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127869 | ACAGGTTGAATATCC[C/T]TTATCCAAATGCTTG | 57630 |
| rs773212105 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264626 | CCGATCTCTCCATTC[C/T]TTGACACAAGCTCCA | 57630 |
| rs773213212 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227029 | AACTAGCCAGGCGTC[-/G]GGGGCACAAATCTCT | 57630 |
| rs773265338 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237683 | AACTTATTAAGGAGA[A/G]TGCCTTAAGACCAGA | 57630 |
| rs773269696 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196092 | AGTGTTGAGATTACA[G/T]GAGTGAGCCACCACG | 57630 |
| rs773296095 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103666 | TAACATTTTCCTATA[C/T]GTTACCGCACATTTT | 57630 |
| rs773297422 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130997 | TGGTACCTGCCTCCC[G/T]AAGAAAACAATAACC | 57630 |
| rs773303228 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164038 | AGGCATTGCCTCCTT[-/G]GGGAAGCTTCTCCCA | 57630 |
| rs773347410 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148120 | TGTTTCATAATTTGT[-/TA]TGAAACATTAAAATG | 57630 |
| rs773359714 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182398 | TGTTTCAGCACATAT[A/G]TAATTAAGAATGCCA | 57630 |
| rs773371853 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109257 | ACAATCTCAGCAAGC[C/T]ACAGCTAAAGCTGTT | 57630 |
| rs773436655 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210412 | TTATTTGTAGAATGA[C/T]TGAAAAATCTGAGTA | 57630 |
| rs773439868 | snp | C/T | 5.21535e-05 | 0.00510627 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117812 | ACATAGATGGAAAGC[C/T]CAGTCCATCAGCAAA | 57630 |
| rs773441291 | snp | C/T | 1.6628e-05 | 0.00288335 | missense | SH3RF1 | GRCh38.p7 | 4:169136456 | GGAGGACTTGTTGGC[C/T]ATAGTGAGGGAAGTG | 57630 |
| rs773493318 | snp | A/C | 1.6817e-05 | 0.0028997 | missense | SH3RF1 | GRCh38.p7 | 4:169136548 | GGGCTGCTGCCGAGG[A/C]ACATTCTCCAGCATC | 57630 |
| rs773508798 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144655 | CAATGAATGAAGAAG[A/G]CCAGATAGAGACCAA | 57630 |
| rs773536025 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198273 | GCCTAATTCTTAGCA[C/T]ACTGGCACAATGAAT | 57630 |
| rs773566994 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202301 | TGTTTACCTCCCTCC[A/G]TAGGAGGCTAGTTCT | 57630 |
| rs773605160 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223199 | CTCATCAAGTGCAAG[A/G]TGCTGCACTCAACAT | 57630 |
| rs773643751 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268670 | ATTCCAAGATGGGGG[A/G]AAAAAATATTCAGAG | 57630 |
| rs773663419 | snp | A/T | 1.65877e-05 | 0.00287986 | missense | SH3RF1 | GRCh38.p7 | 4:169116462 | GCACTGGCTCGACTG[A/T]TACTGATGGCAGCAG | 57630 |
| rs773663421 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188784 | GGCAAAATAATTTCT[C/T]CCATACTCCCTCTAT | 57630 |
| rs773670639 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236800 | CTATATTATTATTCC[C/G]ATAATAAAATGCTAC | 57630 |
| rs773708420 | snp | A/G | 1.6537e-05 | 0.00287545 | missense | SH3RF1 | GRCh38.p7 | 4:169116390 | GGCTCAGCCTCCAGA[A/G]AAGCACTGGTGATGC | 57630 |
| rs773712288 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250029 | AATATGCTCAAGTCA[C/T]GACACAGCCAAGATT | 57630 |
| rs773716199 | snp | A/G | 1.73987e-05 | 0.00294942 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122186 | TCCAGCAGCAGCAGC[A/G]GCGGCGGTGGCGCCT | 57630 |
| rs773744936 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189738 | CTTGGGCAAGTTGCT[C/T]GAATCCCCAAAGTTT | 57630 |
| rs773746397 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235263 | AGTGATATCCTTACA[C/G]ACTAAACTCGTCATC | 57630 |
| rs773776957 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146557 | AAAAAAGAATAGTGG[A/T]AGATGTTATTGAGAG | 57630 |
| rs773804723 | in-del | -/CTCACTGGGGGGCTCCAGGATTGCACCCGAGGCTGCTG | 1.68493e-05 | 0.00290248 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169156680 | AACTGAGGTATACCC[lengthTooLong]TTTAAAAAAAAAAGA | 57630 |
| rs773811915 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175680 | CATGACATTTATCAT[A/G]ACTAGGCACCGACCC | 57630 |
| rs773822210 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169252560 | TCTGCCTGATTGCCA[C/G]ATAATAGTCAACTGA | 57630 |
| rs773830857 | snp | A/G | 1.65979e-05 | 0.00288074 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169116467 | GGCTCGACTGATACT[A/G]ATGGCAGCAGTGTGC | 57630 |
| rs773840878 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223668 | AATATCTAAAGGAGC[C/T]TACTTTCTAATGGGG | 57630 |
| rs773889840 | snp | A/G | 2.43265e-05 | 0.0034875 | missense | SH3RF1 | GRCh38.p7 | 4:169122236 | CAGTGGCAGCCAGGA[A/G]AGGGGGTGGTGGAAG | 57630 |
| rs773898033 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240426 | TGGTCTCAAACTCCT[A/G]GGCTCAAGCAATCGA | 57630 |
| rs773902261 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169099437 | CATCATGAATTTATC[C/T]GAAAGAAGGATCCAG | 57630 |
| rs773914012 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207002 | TTTCACTCGTCACCC[A/C]GGCTGGAGTGCAATA | 57630 |
| rs773938243 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227785 | CCCAGTTACTTTTAA[A/G]AGGAATGTCAAAGGG | 57630 |
| rs773938852 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237427 | GGGAGGATGGCTTGA[A/G]GCCAGGAGTTCAAGA | 57630 |
| rs773990296 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100829 | AAGTCCCAAACACTC[C/T]CCTAAGCCTGAACAT | 57630 |
| rs774006442 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263857 | CTGTGCATCTGGTAT[A/G]CTGTCACATAAACTT | 57630 |
| rs774043434 | snp | C/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169272623 | GTGGAACTGGGCAGA[C/T]AGATGAAGATGAGGC | 57630 |
| rs774063261 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243924 | AATTCAGATACTTTT[A/G]CTTAAATAACTGCAA | 57630 |
| rs774102778 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263034 | GTTTTAATTCAATCA[C/T]TCTGAAACACACAGA | 57630 |
| rs774105709 | snp | A/G | 1.91294e-05 | 0.00309263 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106798 | AATGTTCCAGCCTAA[A/G]GCCTATTGTTCATTT | 57630 |
| rs774114035 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157922 | ATTTTTGTATTTTTA[-/C]AAAATGGGGTCTCGC | 57630 |
| rs774124178 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220278 | TAACTGGAAAAAAAA[C/T]GTCAAGTGGTGTCCA | 57630 |
| rs774126001 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095983 | CAAATTAGAGAACTG[A/G]GATTTCTATCTTAAA | 57630 |
| rs774134118 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162082 | TTGCGAGGCTGAGGC[-/A]GTAGGCAGAGGTTGC | 57630 |
| rs774151012 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231743 | AAATCACCTGGACAA[C/T]TAACGCCTCTTTCTA | 57630 |
| rs774162884 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117554 | GCGGGCCTGGTTGAC[C/T]GTCATTTGCCCCGTC | 57630 |
| rs774164558 | snp | C/G | 1.70145e-05 | 0.00291667 | missense | SH3RF1 | GRCh38.p7 | 4:169106919 | TGGCGAGGAGGTGGA[C/G]CGATGGGAACTGCGG | 57630 |
| rs774169248 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126003 | ACTCTGTAAATTCCA[C/T]AAGGTCTCTATGTTT | 57630 |
| rs774176244 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254956 | CAGCCTGCAAGGTCA[-/G]GAAGAAGAGGTACAG | 57630 |
| rs774190736 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179872 | ATTTTTTTTCCTAAG[A/T]CATATTCCACCCACT | 57630 |
| rs774203570 | in-del | -/C | 1.82777e-05 | 0.003023 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136660 | CACAAGAAGGTTAAA[-/C]AATTCCTAAGAATTC | 57630 |
| rs774215344 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147855 | CACGATATAAGACAT[A/G]ACTTAACATTTGATT | 57630 |
| rs774254580 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153831 | GAAAATACTTTCTAC[C/T]TGGGCAGAAGTTTAT | 57630 |
| rs774270262 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124584 | AATACAATTGGGCAG[A/T]TCTTTTCCCAGTGCA | 57630 |
| rs774292615 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270589 | AGTCCCCAGAGAGAC[C/G]GCGCCATCCGGGAAG | 57630 |
| rs774293100 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121413 | TGGGAAGCACAACAC[A/G]CTGGCTTCTACACAC | 57630 |
| rs774304491 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158962 | CCATGTGATGTTGTA[A/G]TTGGTTAATTAGAAC | 57630 |
| rs774356695 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139988 | CTCTAAATAGCCTAG[C/T]ATATTTTTTCTGCAT | 57630 |
| rs774381948 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175357 | GCTCCCAAGGCTTTC[C/T]ATCATCTGGTCCCGG | 57630 |
| rs774392283 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144358 | TATTCTCAACCCAAA[C/T]AAAAATATCCCATTC | 57630 |
| rs774404284 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209152 | AAATCAGCCAGACAC[A/G]GTGGCACGCACCTGT | 57630 |
| rs774411038 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | SH3RF1 | GRCh38.p7 | 4:169268941 | GCATTTGTGCAGTTG[A/G]TCCCACTTCCCCCAC | 57630 |
| rs774419192 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169112597 | AGATGAAAACATAGA[A/G]GCATCTAAAGGTACT | 57630 |
| rs774419634 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169095136 | ACAATTGTAAGGTGT[A/G]GGCAAATTCACTCCC | 57630 |
| rs774453164 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115221 | TATTTCAAGTCTTAC[C/T]TCTCAAGGAACCATG | 57630 |
| rs774470263 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225342 | AGCTCCAGCACAAGT[-/G]GAGGGCTGGAGGCAA | 57630 |
| rs774482106 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129987 | AGGAGGTGGAGTGTG[A/C]CAGATTAACATGACT | 57630 |
| rs774544940 | in-del | -/AA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211756 | GATGAAAATATTCTC[-/AA]GTTTTATTTCAGTAT | 57630 |
| rs774566702 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166360 | TAAGGTGAAAACGGG[C/T]AACTTCAAGGCTAAA | 57630 |
| rs774571708 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130928 | GGGGATGGGTTCCTG[A/C]ACAAATGGAAGTGTT | 57630 |
| rs774598721 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259652 | TACATGTACTCTTTA[C/T]AATAAAAGCTTTGGG | 57630 |
| rs774599495 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156827 | AAAAACAATATATAT[A/G]TGTTACCAATAAATA | 57630 |
| rs774617107 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214685 | CCATATATATGTGTA[-/T]TATATATATAAGTAT | 57630 |
| rs774654667 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155139 | AATAAACTTTTCTCC[A/C]TCTTACTTAAGAACT | 57630 |
| rs774667287 | snp | C/T | 1.65343e-05 | 0.00287521 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120996 | GCAACATACCTAGAA[C/T]AGAAAATAATATTTG | 57630 |
| rs774681830 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223740 | TCAGGTTGTGATAAG[C/T]GCAAATAAAAATAAA | 57630 |
| rs774690472 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253316 | ATTTGTAAGTATCAG[A/T]TAGCTTAGTCTCCTG | 57630 |
| rs774692694 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210267 | TATTCATTTCCCTTA[C/T]ATATTTGCATCATCT | 57630 |
| rs774710911 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215084 | TAAGTATGTTGTTAT[C/G]TGTAGGATTTGGGGT | 57630 |
| rs774760711 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131109 | TCAGGACAAAGAAAA[G/T]CTCAGAGGTTAGTTC | 57630 |
| rs774798558 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251247 | CCCTTTAGGTTTTAC[A/G]GGGAGGGTGGAAGGT | 57630 |
| rs774798590 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201235 | ATCAGAAAAACACCA[C/T]GGCCTCTCCATCTAC | 57630 |
| rs774802272 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138429 | CTGGCAATGCTGGAG[-/A]AAAAAGGAGCCAGAG | 57630 |
| rs774810469 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118989 | AATGATAACAATTCT[G/T]TATATAGTAACTTTC | 57630 |
| rs774843317 | snp | A/G | 1.81972e-05 | 0.00301633 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136648 | CCAACAAACCAACAC[A/G]AGAAGGTTAAACAAT | 57630 |
| rs774847321 | snp | A/C | 1.70933e-05 | 0.00292341 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120772 | CCATGGAAAAGAACA[A/C]AGCTTCTCTGTTTAG | 57630 |
| rs774851034 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158060 | TTTACTTTTTACCAC[A/G]CAATGTGCAAGTGCT | 57630 |
| rs774855825 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227951 | ACAAATCACAGTCAT[A/G]AAGTGATTCAGAATC | 57630 |
| rs774856478 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167468 | ATAAACGAAAACATA[C/T]ATCCACACCCAGATT | 57630 |
| rs774870128 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142811 | CAGACATGAAAATAT[C/T]TTGCCTCACATTATA | 57630 |
| rs774885262 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169200659 | GTGATACACTGGCAC[A/G]TATATTTGTGAACAG | 57630 |
| rs774886792 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265052 | ACGCTAAATGCAGGT[A/C]TTTCTTCTATCCTCT | 57630 |
| rs774892022 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245447 | TCCATCTAAATTTAT[C/T]TATATAGTCCACTAA | 57630 |
| rs774905224 | snp | C/T | 1.70351e-05 | 0.00291843 | missense | SH3RF1 | GRCh38.p7 | 4:169116547 | GATGGGACAGGCCCA[C/T]AGATGCAGGGCTGAG | 57630 |
| rs774946170 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156233 | AAGTCTGTGCATAAA[A/G]TTACCTTCCTTGTGA | 57630 |
| rs774965103 | snp | C/T | 0.000105071 | 0.00724739 | missense | SH3RF1 | GRCh38.p7 | 4:169116565 | ATGCAGGGCTGAGGC[C/T]GGCGGCATTCTGTAC | 57630 |
| rs774969256 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191259 | ACAGCGACCCAGCTG[A/G]TAATCAAATCAAGAA | 57630 |
| rs774979930 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233105 | AATACAAAAATCAGC[C/T]AGGCGTGGTGGCAGG | 57630 |
| rs775055271 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191639 | ACATTACCTGACTTC[A/G]AACTATACTAAAGCC | 57630 |
| rs775067989 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234322 | AACACCCTCCCCACC[A/C]CCCAAAAAGAATTAT | 57630 |
| rs775075109 | in-del | -/GGGGCGAGTCTGCGGCCGTAAATGTGCA | 1.6517e-05 | 0.00287372 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169120991 | TATAGCAACATACCT[-/GGGGCGAGTCTGCGGCCGTAAATGTGCA]AGAATAGAAAATAAT | 57630 |
| rs775075408 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127976 | AAAAATCTGAAATCC[A/G]AAATGCTCCAATGAG | 57630 |
| rs775093482 | in-del | -/AA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230858 | GAGAAACCACCTCAA[-/AA]AAAAAAAAAAAAAAA | 57630 |
| rs775105230 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236509 | TAAGTAATATCGTTA[A/C]TTATTAGTTGGTGTG | 57630 |
| rs775107142 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098082 | ACTCTAAGCCAGAAC[C/T]AACCAGATGAGCTGT | 57630 |
| rs775113491 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111837 | CATAGAGTTTCAGAT[A/G]CCTGTTTATCAAACC | 57630 |
| rs775131477 | in-del | -/TT | 1.65181e-05 | 0.00287381 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155586 | CATCCTGAAGAAACA[-/TT]GCAAATCATTAATCT | 57630 |
| rs775142717 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158746 | TGTCTGCCCCCCGAC[C/G]TGTAAAAAGTGGATC | 57630 |
| rs775158844 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190454 | AACACCTTTACATGC[A/G]TAAACTAGAAAACCT | 57630 |
| rs775186583 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242642 | CAATGCAACAGTGAT[A/G]GGAGATGGGCCCAAT | 57630 |
| rs775195119 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237369 | TTTCAGGCTGGACAC[A/G]ATGGCTCATGCCTGT | 57630 |
| rs775238489 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147781 | TGTTCAAGTCATTTA[C/T]ATGCCACACATGCAC | 57630 |
| rs775238946 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236271 | AAACATGTCACTTCC[-/A]GATGGAAGCTTTAAG | 57630 |
| rs775243727 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169205958 | GGGCCTTTTACAACT[A/G]GTTCTCTCCTTCACT | 57630 |
| rs775246798 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176971 | CAGGGTTTCGCTATG[A/T]TGCCCGGGTTGGTCT | 57630 |
| rs775276469 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251067 | GACTCAGTTATGCGA[-/C]TGAAGTCTAATGGAC | 57630 |
| rs775281853 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121611 | CAACATTAACCTATA[A/G]TTCTTACCAGTGCTC | 57630 |
| rs775294638 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169138874 | TGCTGCTTTCTCAAC[A/G]GAACAATACTGGGTG | 57630 |
| rs775333684 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169604 | ACTGTTTCAAAAAAT[A/T]AAAAAAAATAAAAAA | 57630 |
| rs775339251 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265318 | AATAAACTAAGTATA[A/T]ATTAGTATAAATCAG | 57630 |
| rs775348934 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141273 | GATTTTTAATACAAA[C/T]AAAACCAAGCAATCC | 57630 |
| rs775351838 | snp | C/T | 1.89138e-05 | 0.00307515 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269225 | CATCTTTATCTACTT[C/T]ACTGAGAAAAAATCT | 57630 |
| rs775357449 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182394 | CATGTGTTTCAGCAC[A/G]TATATAATTAAGAAT | 57630 |
| rs775382087 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229311 | CCAATACTTTTGTAG[A/G]TCACCTTCTTTAATA | 57630 |
| rs775405513 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152185 | AAGGGCCTGTCTAAA[C/T]TGAATAGAACCCATA | 57630 |
| rs775410135 | snp | A/C | 5.15415e-05 | 0.00507623 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117787 | TTGTCACCGCCCTGC[A/C]AAGACACAAACATAG | 57630 |
| rs775412313 | snp | C/T | 1.69798e-05 | 0.00291369 | missense | SH3RF1 | GRCh38.p7 | 4:169106923 | GAGGAGGTGGAGCGA[C/T]GGGAACTGCGGAGTC | 57630 |
| rs775413767 | snp | C/G/T | 0.00011017 | 0.00742124 | missense | SH3RF1 | GRCh38.p7 | 4:169122194 | CAGCAGCAGCGGCGG[C/G/T]GGCGCCTGGTGGTGT | 57630 |
| rs775418169 | snp | C/T | 1.88493e-05 | 0.0030699 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268784 | ATGTGGACATTACCA[C/T]CTTTATTCACCAAAC | 57630 |
| rs775427837 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201086 | CACCATTTCTGATTA[A/C]TGGCAATTTGAAAAA | 57630 |
| rs775447238 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183136 | CATGGCGAAACTCCA[A/T]CTCTACTACAAAAAT | 57630 |
| rs775460725 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096364 | CTTCTTCATTCTGCT[C/T]GCTGGGGTAACTGTG | 57630 |
| rs775468908 | snp | C/T | 8.25076e-05 | 0.00642238 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156650 | TTCATAGTTGTATAA[C/T]GCTTTGGCACATGGT | 57630 |
| rs775487107 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169142520 | TCCGTCTGTGAACCA[C/T]ATGCCCATCTGGTTT | 57630 |
| rs775500951 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123068 | ACTGCCTGAACCGCT[A/G]CCTCGTCCTCTCCAG | 57630 |
| rs775528663 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154938 | TTTACTATGTCAAGC[A/T]TGGCCACAAGCTTTC | 57630 |
| rs775535137 | snp | A/G | 1.81408e-05 | 0.00301165 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136295 | GTGAGCTCTTTTTAT[A/G]TAACACTTGTTTGAG | 57630 |
| rs775548284 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221641 | AAACACTATGCTCCT[C/T]ATAACATACCTTGTA | 57630 |
| rs775575003 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128027 | TTTGCACTCAAAATG[C/T]TTCAGATTTGGGAGC | 57630 |
| rs775592022 | snp | C/T | 1.78468e-05 | 0.00298715 | missense | SH3RF1 | GRCh38.p7 | 4:169269200 | AAAGATCCAACAAGG[C/T]TGATTCATCCATCTT | 57630 |
| rs775594951 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169106192 | ATCTCCACTCACTGC[A/C]ACCTCTGCCTCCTGG | 57630 |
| rs775646945 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245211 | TAAATACAACTTTAA[C/T]GCTACCAACTACTAA | 57630 |
| rs775689544 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230076 | CCAGGCGTGGTGGTG[C/T]ATGCCTGTAATCCCA | 57630 |
| rs775693631 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148832 | AAGGTGAGCTTTCTA[C/T]ACAGACAAAGAAATA | 57630 |
| rs775697362 | snp | C/T | 1.65712e-05 | 0.00287843 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169121008 | GAATAGAAAATAATA[C/T]TTGATTTCAGGTTGA | 57630 |
| rs775706043 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184828 | TAGCATCACCTAAAC[C/T]TAAACTGGACTAAGC | 57630 |
| rs775714117 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178067 | CCAACATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 57630 |
| rs775722795 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257654 | TATGGTTAGGTAATT[C/G]TAAATATGGTTCTAA | 57630 |
| rs775781161 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117437 | TTAAAATTACATCTA[C/T]ATTTCTCAACATCTG | 57630 |
| rs775794015 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160478 | CTAGGGTTACATTTC[C/G]GTGATGCAACTGAAA | 57630 |
| rs775794113 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172371 | TACATGGATATACCT[A/G]TACTCAGAAAATATC | 57630 |
| rs775798493 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201243 | AACACCACGGCCTCT[C/T]CATCTACTGCCAGAG | 57630 |
| rs775814412 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256222 | TTTCCCCAATCACAG[A/G]GAAGGAGGCAGAGAA | 57630 |
| rs775822404 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155598 | AACAGCAAATCATTA[A/G]TCTACCTGATCATTA | 57630 |
| rs775833216 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254889 | TGAGGACATGTAAAC[A/G]AAACTCAGTTATTCA | 57630 |
| rs775840022 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222541 | AATCATTAACTGTTC[C/T]GTATATTTTGACAAC | 57630 |
| rs775847638 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226691 | TCAATTTTATAGGAA[A/T]CTATTGTAGATAATA | 57630 |
| rs775859538 | snp | A/G | 1.85115e-05 | 0.00304227 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116233 | AAAACAGGGAAGTAA[A/G]TAAAGCAGAGAAACA | 57630 |
| rs775929437 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264243 | GGCAACTCTCCTTGG[C/T]TGGTAAGTGGCATCT | 57630 |
| rs775987752 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167840 | CGTACACTTAAGAAC[G/T]GTAATTCACACATAC | 57630 |
| rs776011466 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154104 | AACTATTCAAATGCT[C/T]GGAAGTGCTTGTAGT | 57630 |
| rs776013141 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165994 | CTCAAATGTAAAAGC[C/T]AAAACTGTAAGTTTT | 57630 |
| rs776025923 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213076 | GCACTAGATCATATA[A/G]TAAGAGTATGTTTCG | 57630 |
| rs776033582 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172105 | GGTAGAAGTACTCTA[A/T]ATTTTCCACTCTGAA | 57630 |
| rs776081291 | snp | A/T | 1.84004e-05 | 0.00303313 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136661 | ACAAGAAGGTTAAAC[A/T]ATTCCTAAGAATTCC | 57630 |
| rs776094978 | snp | C/T | 1.66832e-05 | 0.00288814 | missense | SH3RF1 | GRCh38.p7 | 4:169136539 | TGCTGCTCTGGGCTG[C/T]TGCCGAGGAACATTC | 57630 |
| rs776102059 | snp | A/T | 3.35306e-05 | 0.00409441 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096514 | CTTCTTCAGTGTCAG[A/T]CTCCTCATATGTTTT | 57630 |
| rs776102707 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | SH3RF1 | GRCh38.p7 | 4:169120900 | TTGAACCAGCCATCC[C/T]GGCAGCGCTCAAACA | 57630 |
| rs776132457 | snp | C/G | 3.41105e-05 | 0.00412966 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169096490 | TTTGTTGTGTGAAGT[C/G]ATTTTAAGCTTCTTC | 57630 |
| rs776144108 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154439 | AAAACAAATGCCTCA[G/T]ATAAAAAGACTGCAA | 57630 |
| rs776151614 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118593 | CCCGAGTAGCTGGGA[A/G]TACAGGCACGCGCCA | 57630 |
| rs776179112 | snp | A/T | 1.68114e-05 | 0.00289921 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096711 | GAAAGAGATTTTGGT[A/T]AAGGCGATTCAAAGC | 57630 |
| rs776189832 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169182318 | AATACACTCACAAAG[A/G]AGGGTGACCCAAAAA | 57630 |
| rs776197009 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203857 | ATTACAGAAAATAAC[A/G]CAGACACTGGTACTA | 57630 |
| rs776209699 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169103304 | ATGCTTGTTCTCATT[A/G]TAATCTGTAGATGAA | 57630 |
| rs776251576 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248062 | AAATTAGTTCCACCA[C/T]TGTGGAAAACAGTGT | 57630 |
| rs776277683 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169372 | GAGGCTGAGGCAGGC[A/G]GATCATATGAGGTCA | 57630 |
| rs776310148 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202456 | CAGGCTGGGCAGCAC[C/T]GTTTCAATTTACCAT | 57630 |
| rs776358902 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169109384 | AATTCATCTAAAATG[A/G]TTAAACACATTAAAT | 57630 |
| rs776370179 | snp | C/G | 1.64912e-05 | 0.00287147 | missense | SH3RF1 | GRCh38.p7 | 4:169117523 | TGGGTTCCTCCTTAC[C/G]TGTCCTCACAGCATT | 57630 |
| rs776385531 | in-del | -/TGTGTGTGTGTGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187545 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGT]GTGTGTGTGTAGTTG | 57630 |
| rs776386452 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217818 | TAATGCCACAGAACC[A/G]TATACTTTAAAATGT | 57630 |
| rs776391701 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188811 | CTATCAATTTGGTGC[A/G]TGTGCTTCAAGCTTT | 57630 |
| rs776403199 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251128 | ACATGTCACACTAAC[C/T]GAGGTTCAAGGGAGC | 57630 |
| rs776412061 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193526 | TATATACAGATATTA[A/C]GTCTGCAAGTTAAAA | 57630 |
| rs776417908 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209027 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57630 |
| rs776425133 | snp | C/T | 1.87019e-05 | 0.00305788 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116662 | GGGAACACAGCAAAA[C/T]TCAACTATCTAATAG | 57630 |
| rs776438074 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129238 | CACTGGAGCAAATAG[A/G]AAATATAAGCCAAAG | 57630 |
| rs776451351 | snp | C/T | 1.84283e-05 | 0.00303542 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268820 | CTGTAGGCTACTTAC[C/T]CTCACTGGGGGGCTC | 57630 |
| rs776461126 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268545 | CAAAAGCTGGTTTAG[-/AT]TTCATTCACTAATTG | 57630 |
| rs776473567 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181094 | ATATAAAATTCGAAT[A/G]TTCTTAGACATACTA | 57630 |
| rs776476932 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161460 | CTTCCATTTCCATAC[C/T]ATCAGCGGTATTCCA | 57630 |
| rs776495154 | snp | C/G | 5.06231e-05 | 0.0050308 | missense | SH3RF1 | GRCh38.p7 | 4:169107145 | ATGCTGGAGGAGACA[C/G]GCGGGGCTTCCGTTT | 57630 |
| rs776517356 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113539 | AGACACTCGCTAACA[A/G]TAAGTCACAGCAGAA | 57630 |
| rs776529066 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169268925 | GCTCTGAGACCTTAA[C/T]GCATTTGTGCAGTTG | 57630 |
| rs776550062 | snp | C/T | 1.7129e-05 | 0.00292647 | missense | SH3RF1 | GRCh38.p7 | 4:169130095 | AAAGTAAACGAGGGG[C/T]CAGTTGTCACTGGGC | 57630 |
| rs776566739 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239740 | AAGTAATTAAGATCG[G/T]CCGAGTGCAGTGGCT | 57630 |
| rs776578870 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169135722 | GAATGCCCCAGTCAT[C/G]CCATGTATTTTTATA | 57630 |
| rs776581458 | snp | C/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213000 | AGCTGTTATAAATAT[C/G/T]CATGTGCAGGTTTTT | 57630 |
| rs776589302 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169195724 | TTATAAACCTATGTA[C/G]TGAGTTGTTTATTTT | 57630 |
| rs776592275 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261084 | GACCAAACTCAGCCC[C/T]CTCACCAGCCCCATT | 57630 |
| rs776601338 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260167 | CACAGGCAACAGCAA[A/G]ATAGTCAGGGGCTTG | 57630 |
| rs776604300 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244018 | CTAAAGAGTAGTAAA[C/T]GAGGTTTTGAACTGC | 57630 |
| rs776604909 | snp | A/G | 0.00021751 | 0.0104263 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122287 | ATAGGAAAAACATAA[A/G]GAGAAAGGGAAAAAA | 57630 |
| rs776633964 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151287 | AATACTCACAGAGAG[-/A]AAAAAAGGGTTAATA | 57630 |
| rs776667052 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164886 | GGCCTTAGTACCCAA[C/G]TGACAGATAAATCAT | 57630 |
| rs776677165 | snp | A/G | 1.65051e-05 | 0.00287267 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117680 | TCCCTGGAGCTTCTG[A/G]GCAGGCCCTCCTGCC | 57630 |
| rs776690197 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228300 | ACTTCATGGCTTAAG[A/T]TAACACAAATTTGTT | 57630 |
| rs776713531 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242691 | GGGGGCTCTGCCCTC[A/T]TAAATGGACTGTCCT | 57630 |
| rs776721822 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117390 | CAGATACAAGGTGCC[A/C]CTGAGTAGACTTTGC | 57630 |
| rs776778850 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254357 | ACTAAAGCACAATTA[A/G]TTAGAGAACAATACC | 57630 |
| rs776791882 | snp | A/G | 1.91002e-05 | 0.00309026 | utr-variant-5-prime | SH3RF1 | GRCh38.p7 | 4:169269230 | TTATCTACTTTACTG[A/G]GAAAAAATCTTCAGA | 57630 |
| rs776811384 | snp | G/T | 3.44453e-05 | 0.00414988 | missense | SH3RF1 | GRCh38.p7 | 4:169136427 | TCCATGGAGTGGCGG[G/T]TCTGGGATGCCTGGG | 57630 |
| rs776818427 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110674 | AGAAAATCTGTGGTT[A/G]ACTCCTTAAGGGAGA | 57630 |
| rs776853881 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190106 | GTTCATAGCCCTAAA[C/T]GCCTACATCAAAAAG | 57630 |
| rs776856646 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169270103 | GCAAGCCACTTACTG[C/T]GCCGCTCTCCCCCCA | 57630 |
| rs776880276 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224037 | ATTGACATTTGGGGC[A/T]GAATACTGTGGTCTT | 57630 |
| rs776902654 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220501 | TATTTTGGCAAGTGT[C/G]GACTAGGGAGTGGGG | 57630 |
| rs776907038 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097912 | ACACTCAACATCTCT[A/G]TGGAGAGGAAACACA | 57630 |
| rs776912849 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235454 | TCTGTAAGATAGGTA[C/T]TATTATTATTTCCAT | 57630 |
| rs776914774 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248703 | GGAAACATCCACGTG[A/G]GCAGTCCAGTTTCCC | 57630 |
| rs776942212 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169183611 | TAATTAGCTGGGTGT[A/G]GTGGTGTACAACTGT | 57630 |
| rs776944631 | snp | C/G | 1.64841e-05 | 0.00287085 | missense | SH3RF1 | GRCh38.p7 | 4:169268960 | CACTTCCCCCACCAG[C/G]ACCAGGTTTCCAAGG | 57630 |
| rs776957657 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174234 | ACCTGGCTAATTTTT[C/G]TATGTTTTGTAGGGG | 57630 |
| rs776960055 | snp | A/G | 1.64939e-05 | 0.0028717 | missense | SH3RF1 | GRCh38.p7 | 4:169122100 | GACACGCTCACTTAC[A/G]CACTGGGGCGAGTCT | 57630 |
| rs776979798 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233018 | CTTTGGGAGGCCGAG[A/G]CAGGCAGATCACCTA | 57630 |
| rs776981723 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162168 | TCTCAGAAAAAAAAG[G/T]AAAAAAAAATAGAAT | 57630 |
| rs776992824 | in-del | -/CAC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113352 | TGACCTCAGGTGATA[-/CAC]CAGCTTTGGCCTCCC | 57630 |
| rs777019485 | snp | C/G | 1.8396e-05 | 0.00303277 | missense | SH3RF1 | GRCh38.p7 | 4:169116613 | CTGCCGTGGGGCGTT[C/G]CTGGTTGTGCGCTGC | 57630 |
| rs777060010 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260257 | TTTTCTGAGACCAGA[A/G]ACTTAATTATGGGGC | 57630 |
| rs777062653 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256113 | ACAAAGCACATCTAG[C/T]TTCCCTTACGGAAAG | 57630 |
| rs777064085 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176872 | GATTAAAACCACTTG[A/T]GCTGGGCATGGTAGC | 57630 |
| rs777064817 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134103 | GTTTTCTGTAAACCT[C/T]GGCTGGAGAAACCAG | 57630 |
| rs777097420 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169127400 | GCTGTTAATAGTACT[-/C]ACAGTCTTCGGAACC | 57630 |
| rs777117656 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227141 | ACTGTACTCCAGCCC[A/G]GGTGACAGAGCAACA | 57630 |
| rs777135608 | snp | C/T | 1.65485e-05 | 0.00287645 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156464 | TTCAAAGTCATAAAG[C/T]GCTTTGCACTGAGGT | 57630 |
| rs777136454 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108724 | CAATGCCACATTTTC[C/T]GTGGGGCTACTGTGT | 57630 |
| rs777183927 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203185 | ATTCACATAGCTGCT[-/A]AAGTGTATCACAGAG | 57630 |
| rs777188380 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176635 | AACCTCAGTTTCCCA[C/G]GTTCAAGCGATTCTC | 57630 |
| rs777218014 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162918 | CTGCTGCCCTGCTCA[C/T]GCTCATCTGTGGGCT | 57630 |
| rs777242873 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210573 | ATGCAAAATATTTTC[C/T]TTTCATAATAACATG | 57630 |
| rs777264114 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209793 | TTTTTCTTCATGCCC[C/T]TTCTTTTATTTTTGG | 57630 |
| rs777285159 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102780 | TCCTTTTGTTCCTAA[C/G]AGAATTCTCTCTGCT | 57630 |
| rs777288048 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220471 | TTTTCCTTTTTCTAG[-/T]ACATTTAGAGTGCAT | 57630 |
| rs777319245 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151737 | TCTATAGCAGAGGAG[C/T]AAGTTGCTAAATAAC | 57630 |
| rs777357389 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169265991 | TTAGGCCATAGACAG[A/G]TATCAGCAGTGTCCC | 57630 |
| rs777358792 | snp | A/G | 1.64819e-05 | 0.00287066 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117641 | AGCTGCGGGGACAAC[A/G]CTGGGACTCCCAGCC | 57630 |
| rs777378063 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114400 | CCTGGATAATTCAGG[C/G]TAACCACCTTGTCAA | 57630 |
| rs777419395 | in-del | -/CC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202787 | GTTGTTGTCATCAGA[-/CC]TACTTAAACTTTGTA | 57630 |
| rs777427834 | snp | C/T | 5.01056e-05 | 0.00500503 | missense | SH3RF1 | GRCh38.p7 | 4:169117748 | GGCCAGCTGTAGACA[C/T]AGGGACTTTAGCTTG | 57630 |
| rs777447248 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240483 | GATTACAGAGCGTGA[C/G]CCCTTGCATCTGGCC | 57630 |
| rs777454282 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206388 | TATCCATTCAAGGGG[-/C]TGGGGGAAGGGGGGT | 57630 |
| rs777473894 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116000 | TAAGTCTCATTCACT[G/T]TGGTCCCTCTAACAT | 57630 |
| rs777511876 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169196744 | CTTCATCAGGAATGT[C/T]AATCCAAATTACTTG | 57630 |
| rs777516247 | in-del | -/CAGG | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271492 | CGGACCCTTCCTCCC[-/CAGG]CTGGGCGAGTCGCGG | 57630 |
| rs777537242 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169241651 | CCAGAAATGCCTCTA[C/T]ACCAAAAGGACAATG | 57630 |
| rs777538505 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229665 | AAGTGAGAAGTGAAT[A/G]CTAATGTAGAGCATA | 57630 |
| rs777549118 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136498 | CTTTTTGGTGTTCTT[C/T]TTGGTGTCGGAGTGC | 57630 |
| rs777562337 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108632 | CCCTGCAACTCTCCC[A/G]GGTAGAGGAAGATCC | 57630 |
| rs777570194 | snp | C/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094880 | TGCAAGACTTTTCAG[C/T]TCATGTTTCTATTTC | 57630 |
| rs777636451 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267744 | AACTGCCTGGTATCC[A/C]CATCTGCGAATTATG | 57630 |
| rs777648216 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220141 | TGTCTATAGGTAACT[C/T]AGAAAAGAGTAACTA | 57630 |
| rs777650200 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222395 | GCTTGAACCTGGGAG[A/G]TGGAGGTTGCAGTGA | 57630 |
| rs777669110 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147552 | CAAGGATATTGACCA[C/T]CAGGACTTTGCACGT | 57630 |
| rs777724612 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247154 | CAAAGGTTCAGACAC[C/T]GAAACTGGAGATGGG | 57630 |
| rs777726792 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234832 | GACATTTGGGCCTGA[C/T]AGTTGTTTGTTGGGG | 57630 |
| rs777737518 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169173341 | AACAAAATATTAATA[C/T]GACATTAGTAAAACT | 57630 |
| rs777738153 | in-del | -/A | 3.62588e-05 | 0.00425771 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136637 | GCAAAAGCAACCAAC[-/A]AAACCAACACAAGAA | 57630 |
| rs777739918 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208842 | AAGTAGGAGTGGGCC[G/T]ACGCAGAAACCCCTG | 57630 |
| rs777786447 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188526 | ATAACCATTAAGAAA[C/T]GATACACTGCTTTTC | 57630 |
| rs777815459 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191201 | CACTCCTCTTCAACA[C/T]ACAAAATTAATGTAC | 57630 |
| rs777824936 | snp | A/G | 6.65004e-05 | 0.00576592 | missense | SH3RF1 | GRCh38.p7 | 4:169116340 | TGTCAGGAGATGTGG[A/G]GAGTCCAGGGAGAAC | 57630 |
| rs777844943 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143336 | GTACTGAGATGGGTA[C/T]ATTCTTTTTTTGTAC | 57630 |
| rs777901029 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175034 | CTCTACCAGTTTTCC[C/T]CAATGTTGGTAAATA | 57630 |
| rs777903715 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267759 | ACATCTGCGAATTAT[-/G]GGAACTAATGCTATC | 57630 |
| rs777903919 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192574 | ACTATGGAAAACAGC[A/G]TGGAGATTCCTTAAA | 57630 |
| rs777921700 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237242 | TTCCCAGACACACGG[C/T]GAAGGTGATTTGAAA | 57630 |
| rs777925437 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251821 | CTGATTTAGGGCTGC[A/G]CAGCCTACTAGAAAC | 57630 |
| rs777930170 | snp | C/T | 1.64779e-05 | 0.00287031 | missense | SH3RF1 | GRCh38.p7 | 4:169096592 | GTGCCTTTGAACCAG[C/T]CATCCTCTCGTTTTT | 57630 |
| rs777956237 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159366 | ATAATAGTAAAACAC[A/T]GCAATCGACAGAGAG | 57630 |
| rs777978741 | snp | C/T | 1.64966e-05 | 0.00287194 | missense | SH3RF1 | GRCh38.p7 | 4:169155541 | CCTTCAGCCCAGTTT[C/T]CATCCACTCTTCGGA | 57630 |
| rs777993773 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179370 | TGGCCCAGGGAGACC[C/T]GTGTTAGACTTCTGA | 57630 |
| rs778012932 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247808 | TTTACAAGAAAAAAA[-/C]GACCCCATCAAAAAG | 57630 |
| rs778020480 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169098609 | AAAAGCACAGCACAG[A/C]AGTTGGCTTATCATA | 57630 |
| rs778029103 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260819 | ACACAGGAAACCAAC[A/G]TAACTGAGTTCATGT | 57630 |
| rs778029246 | snp | A/G | 3.67296e-05 | 0.00428526 | missense | SH3RF1 | GRCh38.p7 | 4:169116610 | CTGCTGCCGTGGGGC[A/G]TTCCTGGTTGTGCGC | 57630 |
| rs778082618 | snp | A/T | 1.67933e-05 | 0.00289765 | missense | SH3RF1 | GRCh38.p7 | 4:169116529 | GTGGGGAGGCCAGCG[A/T]GTGATGGGACAGGCC | 57630 |
| rs778087011 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186191 | CCTATTTTCTAAATA[C/G]AGAGTATGGTAGCTT | 57630 |
| rs778097208 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169219958 | AGCAATCAACTTCCA[A/G]GCGATCAGTACAAAC | 57630 |
| rs778098391 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226328 | GACATTTATAATTCA[C/G]TTGCAAATTCATAAA | 57630 |
| rs778098426 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238274 | GCACTATTAATACTC[C/T]GCACAGCAGGGAGAA | 57630 |
| rs778108244 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100365 | TTTTTTTTTAAGACT[A/G]AGTTTCGCTCTTGTC | 57630 |
| rs778119556 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248616 | CTATGTAACAAACCT[A/G]CACATTCTGTACATG | 57630 |
| rs778147988 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169139510 | CTATCCATTCTACTG[C/T]TGATTAACATGTGGG | 57630 |
| rs778186217 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212841 | TTCAAAAAAATCCTG[C/T]GTGCTCAACTTACTC | 57630 |
| rs778203212 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253007 | GGGTGGGAGGTGGGG[G/T]TGACTGAGAAATTTA | 57630 |
| rs778207171 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203596 | GTTCTAATTGCTCTG[C/T]AATCCCTACCAGAAA | 57630 |
| rs778230049 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107635 | TTATGGATTTAATTT[C/T]CTGAACTTCTGCCTA | 57630 |
| rs778257427 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169169144 | AGCATTCTTCTAGTC[A/C]ATTAAATGTGAAGTT | 57630 |
| rs778285633 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156749 | CTGAAAATACAACTG[C/T]GTTGTCATTGTTTTA | 57630 |
| rs778287409 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222254 | AGATCACTTGAGATC[A/G]GGAGTTGGAGATCAG | 57630 |
| rs778289420 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136803 | GACTTCATTGTATCT[-/A]TATCACAGGTAGATA | 57630 |
| rs778315825 | snp | C/T | 3.53307e-05 | 0.00420287 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107188 | AGAAAGCAACTTCAA[C/T]AAACCCTTTTTTTCT | 57630 |
| rs778345426 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169170312 | AATAGCAAAGAAAAT[A/C]AAGCAAGAGCCCATG | 57630 |
| rs778362849 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167839 | TCGTACACTTAAGAA[C/T]TGTAATTCACACATA | 57630 |
| rs778377032 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208178 | TCCTAAAAGGAAACC[A/T]CATTCCTTCACTAAC | 57630 |
| rs778429047 | snp | A/C | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094814 | ATTTAGGAATGATTT[A/C]ATCTTCAACCACATA | 57630 |
| rs778435443 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158482 | ATTGAGGGTCTTGTA[C/T]AACATATGAAAGAGT | 57630 |
| rs778436449 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150458 | AGCTAATTAACATAC[A/G]TATTACCTCAGATAG | 57630 |
| rs778460298 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161118 | ACTTTCACTTGGCTA[A/C]ACATGAAAGGGATGC | 57630 |
| rs778497898 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169257033 | AGATTCCTTATCTCA[G/T]GTAATCCTCACAAAC | 57630 |
| rs778531321 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143382 | CGGTGCGAACGGAGT[A/G]CTTCCATCCCACTCA | 57630 |
| rs778538708 | snp | A/G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247825 | ACCCCATCAAAAAGT[A/G/T]GATGAAGGACATGAA | 57630 |
| rs778563407 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199488 | CATGGATGAGGTCCA[A/C]GCACTCCCTAAAAGC | 57630 |
| rs778567789 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175818 | CACTATTTGTATCTT[C/T]CCTCTCCCCCCATCC | 57630 |
| rs778571835 | snp | A/G | 6.72699e-05 | 0.00579917 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107068 | TCCTGGTGGCAGTTC[A/G]GGCCCCACCGCTCCC | 57630 |
| rs778592210 | snp | C/T | 1.88809e-05 | 0.00307248 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169268770 | AGAATAAAGAAAAAA[C/T]GTGGACATTACCACC | 57630 |
| rs778601540 | snp | A/G | 4.96028e-05 | 0.00497985 | missense | SH3RF1 | GRCh38.p7 | 4:169120831 | TACCTTGTGACTGGT[A/G]CCACATAATTGCCAG | 57630 |
| rs778619212 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128961 | TCTAACTCTGTGAAG[G/T]AGATACTTATTTTAT | 57630 |
| rs778624802 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209728 | AGATAACACTGTAAT[-/G]TACCGGAAAGTGTTG | 57630 |
| rs778626976 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110488 | AAGAATAATAAGCCA[A/G]GTGCCGTGGTGTGAA | 57630 |
| rs778640297 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169133357 | GCACACACCTGTAAT[-/C]CCAGCTACTCAGGAG | 57630 |
| rs778655126 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184623 | TTAACTATGAGCCAC[G/T]AAAAAGGAGATGCCA | 57630 |
| rs778656524 | snp | C/T | 1.78144e-05 | 0.00298444 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136612 | CAGCTGCTTAGCAGC[C/T]GAGTTAAACTGCAAA | 57630 |
| rs778690526 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206525 | AAAAAATTTTTAAAA[A/C]TTATATAAAAACAAA | 57630 |
| rs778690635 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240456 | ACCTACCTCAGCCTC[C/G]CAAAGCTCTGGGATT | 57630 |
| rs778699773 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169244928 | CAGTTTTTAGAAAAG[G/T]TTTTGCAAAATAAAA | 57630 |
| rs778779591 | snp | A/G | 1.65198e-05 | 0.00287395 | missense | SH3RF1 | GRCh38.p7 | 4:169136512 | TCTTGGTGTCGGAGT[A/G]CTTTGGGGCAGTGCT | 57630 |
| rs778788104 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247769 | AAGGGCTAATATCCA[A/G]AATCTACAAGGAACT | 57630 |
| rs778789830 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246161 | ATATTACTATGCAAG[A/G]TGTTACTTCGTCAAG | 57630 |
| rs778827091 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157071 | AGGATAAATGATAAA[A/C]ACTGAGGAGAAATGA | 57630 |
| rs778847787 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223886 | AGGCAAAAACCCTGG[A/G]GCAGAACAGTTGGGC | 57630 |
| rs778850215 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214126 | GGGGCCTCGAGGGAA[A/G]TGTTTGGGTCATGGG | 57630 |
| rs778875147 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169251601 | AAAAGCTTTTAATGG[A/G]CAGGTACATTTAAGC | 57630 |
| rs778877568 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233633 | CTTAGATGGCTTTGG[C/T]TGTTTGGCTTCTGAA | 57630 |
| rs778881008 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152260 | GGGGAAGGGTGAATG[G/T]GATCAAAGCAAGAGA | 57630 |
| rs778911086 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169155742 | TTTCATGAATTAAAC[G/T]GTAGCTACCAGCCCA | 57630 |
| rs778964252 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221276 | CTCTGCTCCTGACAA[C/T]GTTTATAAACAGAAC | 57630 |
| rs778981387 | in-del | -/CT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269731 | ATCCAACTAAATTCC[-/CT]TTTTTAAGCCACTTT | 57630 |
| rs778987572 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125524 | AGGGCTACAGGCCAG[C/T]TTGCCAGTAAAGTGC | 57630 |
| rs779015519 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238882 | TTCCCCATCCTCTTT[C/T]TTTCTAGTTGACTTT | 57630 |
| rs779032722 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146335 | CCTGGGTTCAAGCAA[C/T]TCTCCTGCCTCAGCC | 57630 |
| rs779039330 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191139 | TGGGGAAAAGTTGAA[A/C]TAATTCCCTCTGAGA | 57630 |
| rs779042479 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123199 | TAACAAAATAAAGAT[A/C]CAATGATTTCTAAAC | 57630 |
| rs779048834 | snp | A/G | 1.67077e-05 | 0.00289026 | missense | SH3RF1 | GRCh38.p7 | 4:169116517 | GAGGCGCAGGTTGTG[A/G]GGAGGCCAGCGAGTG | 57630 |
| rs779065931 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169240739 | TACTGGCCTAGCAGT[C/T]TTCAAGTCCATAACA | 57630 |
| rs779071037 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108776 | CAAACTTGGACTGCC[C/T]GCATAAGTGCAGTGG | 57630 |
| rs779073048 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169123506 | AGCCACTTACAAAGT[A/G]CAAACCAGGAGAAGG | 57630 |
| rs779088725 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101561 | GACAACATGAATGTA[C/T]TCAATGCCACTGAAT | 57630 |
| rs779100374 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148536 | ATTTCCTTTCCAAAC[A/G]TTCTGGAACATGATT | 57630 |
| rs779105405 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169158394 | TGTGCAGCGGGACTG[A/G]GGAGCATAAAGAATG | 57630 |
| rs779151965 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169146634 | ACAGGAGGAAAATTT[C/T]AGAGACTGGAGTGAC | 57630 |
| rs779152893 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102866 | CTTAAGTCTTTATAC[C/T]ACGTGGTTGCTTCTT | 57630 |
| rs779158927 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110181 | GGAGTTGAGAGCAGC[C/G]TGGGCAACATAGCAA | 57630 |
| rs779165963 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | SH3RF1 | GRCh38.p7 | 4:169096622 | TTATGAACAAACACA[A/G]TATCTCCTTCTTTAA | 57630 |
| rs779230848 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176465 | GTGATCAATTTTAAC[C/T]GAACAAAACAAATAT | 57630 |
| rs779242687 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169236206 | TCCGACCTCCTTGAA[A/G]TGGAATCATGGCCTA | 57630 |
| rs779247034 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111296 | ATCTAGTTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 57630 |
| rs779247305 | in-del | -/ATATAT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177856 | ATGTGTATGTATATA[-/ATATAT]ATATATATGCTCACG | 57630 |
| rs779268111 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169115663 | AAGTGCACAGTTAAT[A/G]TAATGAGCTTGAATC | 57630 |
| rs779304845 | snp | C/T | 1.65477e-05 | 0.00287638 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117498 | CCCTTTATCCTGATA[C/T]GTTCTGGCCTGGGTT | 57630 |
| rs779335010 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224794 | GAGATCTTGAAGACT[C/G]AGCCATCAGGATTTG | 57630 |
| rs779348300 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230068 | AAAATTAGCCAGGCG[A/T]GGTGGTGCATGCCTG | 57630 |
| rs779349447 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228801 | ACTCACAGACATATA[A/C]CACACCCATACCCAA | 57630 |
| rs779354595 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113751 | AATTTATATCAACCA[G/T]AAGTCTCTTTAGTGG | 57630 |
| rs779357012 | snp | C/T | 1.71088e-05 | 0.00292474 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169130076 | GTAGGGAACATCTGA[C/T]GGGAAAGTAAACGAG | 57630 |
| rs779359164 | in-del | -/TTTGCTATCCTTGTCTGGTTTGGTTG/TTTGCTATCCTTGTCTGGTTTGGTTGCTGAACTGTTCCCACAAG | 5.52027e-05 | 0.00525346 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169107205 | ACCCTTTTTTTCTTT[lengthTooLong]CTGGAAAAAAAAAAT | 57630 |
| rs779410507 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180774 | ACTTATTCTTCAACT[G/T]CATAAACTTCAATAT | 57630 |
| rs779439927 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186363 | AGTTAAAAAAAAAAC[A/G]AATTTATTTGGGCAG | 57630 |
| rs779441096 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232610 | CTATCCCAGAGCAGC[A/T]GTTTGGCTGCAGCAA | 57630 |
| rs779441579 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217443 | GGTCAGAGAAACAGG[A/C]AATCAAGGCAGGTAA | 57630 |
| rs779457520 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169110854 | TAATGTCAATGTCAG[A/G]CGAGACTTACAAAGC | 57630 |
| rs779493115 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169181787 | ACTCTTCTAAGATTA[C/T]GATGCCAGAGAAGAG | 57630 |
| rs779532957 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169221013 | TTTGAACTCTCGTGT[C/T]GAAAGAGTTGAACAC | 57630 |
| rs779542966 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169262090 | GTATATTATACATCA[A/G]TAAAGAGTTTTTTCA | 57630 |
| rs779550238 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161686 | AAGAAAATCTAGAAG[A/C]CACTCTTGTAGTGGG | 57630 |
| rs779554419 | snp | A/T | 3.29603e-05 | 0.00405944 | missense | SH3RF1 | GRCh38.p7 | 4:169122125 | GAGTCTGCGGCCGTA[A/T]ATGTGCAATCTGGTC | 57630 |
| rs779560184 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169210434 | ATCTGAGTAAATGCT[A/G]ATTCTATAAATTACA | 57630 |
| rs779561092 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105632 | GACATCGTGGCTCAC[A/G]CCTGTAATCGCAGCA | 57630 |
| rs779598281 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169159686 | CATCATTGTCATCAT[C/T]GTCATCATTACCCAG | 57630 |
| rs779601659 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160194 | AAGATACAGATTTAG[C/G]ACTCTTAGAAACCAT | 57630 |
| rs779617519 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185542 | ATAACTAACTGCTAC[A/C]CCCACAAAGCTGGCA | 57630 |
| rs779637249 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269769 | TAAGAAACCATGCCT[C/T]ATGTAATCGCTCGTG | 57630 |
| rs779657546 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125750 | TCTGATTTCCATTCA[A/G]CCCACTTTCAACCCT | 57630 |
| rs779660462 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169129653 | GTATCGGATCTGTCA[C/T]GTGACTCAAAGTAAA | 57630 |
| rs779675015 | in-del | -/AC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193965 | CTCAGCTGTACTAAG[-/AC]AATCTCAAGGATAGA | 57630 |
| rs779694859 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177531 | TGTAAATGCAATAAA[A/G]ATATATTAAATACAC | 57630 |
| rs779715563 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156298 | AGTGAGTAGTTCACA[A/C]AAAACTTGTATTTTT | 57630 |
| rs779722707 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220167 | AACTAATGCAAGGAA[C/T]AGTTTTGTTATAAAA | 57630 |
| rs779766670 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117208 | GTAGAGTATCACGCA[A/G]TGTCACATGGATGGT | 57630 |
| rs779791478 | snp | A/T | 1.64795e-05 | 0.00287045 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169120965 | ATCCTCTTTCCGAGG[A/T]GTGTATGGATATATA | 57630 |
| rs779795965 | snp | A/C/T | 5.0268e-05 | 0.00501317 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169107128 | CACTTCTAGGGTGGG[A/C/T]GATGCTGGAGGAGAC | 57630 |
| rs779805015 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222120 | CTGCTCAAAGCAAAG[A/C]TACTGCAATAGAAAA | 57630 |
| rs779805533 | snp | C/T | 1.65263e-05 | 0.00287452 | missense | SH3RF1 | GRCh38.p7 | 4:169155494 | CCTCAACATATGAAA[C/T]TGGAAATATTCCTAT | 57630 |
| rs779808466 | in-del | -/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102915 | GCCCCAGTCACATTC[-/TT]TTTTTTTTTTTTTTT | 57630 |
| rs779819979 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263437 | TATAGATTATTGAAC[A/G]TAACTGGACCTGAAA | 57630 |
| rs779829224 | snp | A/G | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094335 | GAAAAGGAGTGATAA[A/G]TCGCAATTTTATCAT | 57630 |
| rs779854494 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104509 | AAATGATTTCATTTG[A/T]AGGGAGAGAACACTT | 57630 |
| rs779861773 | snp | C/T | 3.31549e-05 | 0.0040714 | missense | SH3RF1 | GRCh38.p7 | 4:169268900 | TTGAGCTACAATTAG[C/T]CACAGTGCTGCTCTG | 57630 |
| rs779890770 | in-del | -/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169207040 | TGTAGCTCACTGCAG[-/C]CTTGATCTCCCAGGC | 57630 |
| rs779905337 | in-del | -/CT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124983 | GAGGCCAAGTATACA[-/CT]CTCTACTACAGGCAA | 57630 |
| rs779914550 | snp | C/G | 1.65086e-05 | 0.00287298 | missense | SH3RF1 | GRCh38.p7 | 4:169120847 | CCACATAATTGCCAG[C/G]GAAAACCCCTATCTT | 57630 |
| rs779919233 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169264650 | AGCTCCAATCCCGTA[C/T]CTGTTCTGAAGCCCT | 57630 |
| rs779940862 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169243521 | CCTTCTCAATAAATA[A/G]ATAGATAAATAAATA | 57630 |
| rs779974286 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163530 | CTAGAGAGGTAGGAC[A/G]AAAACCAGCAAACTA | 57630 |
| rs779975372 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167246 | ACACCATCAGGCAAC[C/T]GCAAAATAAAACCAA | 57630 |
| rs780037727 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169118037 | TACAGTTATTGCATT[C/T]AGCTTTCCATAACAA | 57630 |
| rs780041943 | snp | C/G | 1.79919e-05 | 0.00299927 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136624 | AGCCGAGTTAAACTG[C/G]AAAAGCAACCAACAA | 57630 |
| rs780059978 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164525 | GTGGTGGGCACTTGA[C/T]TCTGAGACATGGGAG | 57630 |
| rs780078021 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169261829 | GAGATATTGGAAGCC[-/T]TTGATTTTCTCCTTT | 57630 |
| rs780080193 | in-del | -/AAAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190335 | ATTAGCAAGATTAAC[-/AAAG]AAAAGAAGAGAGAAA | 57630 |
| rs780082138 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199342 | CATTCTCATAACAGT[C/G]TAATGTTTGGTTGGC | 57630 |
| rs780088803 | snp | A/T | 3.31252e-05 | 0.00406958 | missense | SH3RF1 | GRCh38.p7 | 4:169122161 | ATCCTGCCATGGGCC[A/T]CGGTCCCATTCCAGC | 57630 |
| rs780092690 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259823 | TATCCATACTATGTC[A/G]CTATGTGTAGTATTT | 57630 |
| rs780104190 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231483 | AGGCTGGAGAATCGC[C/T]TGAATCCAGGAGGCA | 57630 |
| rs780137743 | snp | C/T | | | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122165 | TGCCATGGGCCTCGG[C/T]CCCATTCCAGCAGCA | 57630 |
| rs780139933 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100581 | TCCTGACCTGGTGAT[C/T]CACCCACCTTGGCCT | 57630 |
| rs780152642 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153601 | TTCAGTAGGTTGCAA[C/T]TGAAGTCTGCCTCCA | 57630 |
| rs780176585 | in-del | -/A | 0.068335 | 0.171749 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107209 | TTTTTTTCTTTCTGG[-/A]AAAAAAAAAATAATG | 57630 |
| rs780178443 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202998 | CTATTTGGGATAGAC[A/G]GCTCTTGGAGAAAAA | 57630 |
| rs780201833 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234851 | TGTTTGTTGGGGAGC[A/G]TGGCTGTCCTGTGCA | 57630 |
| rs780205038 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226238 | GACAATGCAAATCAC[A/G]CTATAGATAAAAGAG | 57630 |
| rs780238468 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120284 | GAATTCAGAGGTAAT[G/T]ACCAAGTTAATGAAA | 57630 |
| rs780242296 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136015 | AAGCAGTACTGTGAG[A/C]AAGTTCTGTAAGGCT | 57630 |
| rs780248496 | snp | A/G | 1.65564e-05 | 0.00287714 | missense | SH3RF1 | GRCh38.p7 | 4:169116444 | GCTGCACAGGCCAGA[A/G]GGGCACTGGCTCGAC | 57630 |
| rs780268540 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156841 | TGTGTTACCAATAAA[C/T]AGAAAACACAAAACA | 57630 |
| rs780323103 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108703 | TGCGCTTTCGCTTCA[C/T]TCATTCAATGCCACA | 57630 |
| rs780326982 | snp | C/G/T | 4.95432e-05 | 0.0049769 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169122089 | CAGTAACAGACGACA[C/G/T]GCTCACTTACACACT | 57630 |
| rs780359632 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169234511 | GTTTGGGTGAAGAAC[A/G]TTTACATCTAAACAA | 57630 |
| rs780369731 | snp | A/G | 1.65425e-05 | 0.00287593 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096692 | CCACCCTGTGCCTAG[A/G]AAAGAAAGAGATTTT | 57630 |
| rs780398935 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169128903 | GCAACAGCCCTCAAC[C/T]GAGCCCAAAAAGGAG | 57630 |
| rs780421974 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169114117 | CAGTAAGGACCTGTA[C/T]TAGATGGTGCCGTAA | 57630 |
| rs780435636 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160954 | CTGCCCTCTCATTCA[C/T]CTCCTTCGAAAGGTC | 57630 |
| rs780450011 | snp | A/T | 3.5033e-05 | 0.00418513 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169156413 | CTTTACCTTTGCAAA[A/T]GGAAGGCAATCTTTG | 57630 |
| rs780463302 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169188686 | AATCTTTAAAGCTTT[C/T]TGGCTTATGTAACAA | 57630 |
| rs780475958 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214601 | TTTTATTTCTTTCAT[C/T]GGATTTTTGTAGTTT | 57630 |
| rs780484262 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266326 | TCAGCTTTGCACAAC[A/T]TATGGAAACAGGCTC | 57630 |
| rs780490126 | snp | G/T | 1.65293e-05 | 0.00287479 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169117504 | ATCCTGATATGTTCT[G/T]GCCTGGGTTCCTCCT | 57630 |
| rs780500194 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254912 | GTTATTCAGTCCAGA[C/T]AAAAAGAGAGGAGGT | 57630 |
| rs780502732 | snp | A/G | 9.08488e-05 | 0.00673915 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106858 | TTACCTTTCACAAAC[A/G]ACAGGTCTAGACTCA | 57630 |
| rs780549949 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169117602 | AGCCTGAGGACTTGT[C/T]TGGATGTGAGCTGCT | 57630 |
| rs780553930 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179689 | AGCCCCACGCAAAGA[C/T]AACACTGCGCAAACT | 57630 |
| rs780626927 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153470 | ATATGAATAGGTTTA[C/T]AGAGCTAGAGAAAGA | 57630 |
| rs780653073 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193957 | AGTCTTTTCTCAGCT[A/G]TACTAAGACAATCTC | 57630 |
| rs780676978 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197770 | TCACAAATTCAAAGA[C/T]CTGATACTACTACAA | 57630 |
| rs780681942 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260418 | GAAAGAACAGACCAC[A/C]GTTGCAGGCCAGGGC | 57630 |
| rs780698292 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222512 | ATTTTTATACATATT[-/TA]TATATATATATAAAT | 57630 |
| rs780718611 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134555 | GCTAGGTCCCAAGAT[A/T]AAAAGCACAGAATCA | 57630 |
| rs780723926 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169152750 | CTCAAAAAATAAAAA[A/C]GGAGATTTGTTTGCA | 57630 |
| rs780751325 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169137652 | ATAATATCATGTACT[A/C]TTTTTCCCACTTAAA | 57630 |
| rs780753241 | in-del | -/CTCA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169136937 | GAAAATTTATTTCAG[-/CTCA]CTGTGAAATTTCGAG | 57630 |
| rs780769686 | snp | A/G | 1.80374e-05 | 0.00300306 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169136350 | AGGAGAGCCCAGACA[A/G]CTCGCTGATCCGTGC | 57630 |
| rs780772535 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169203553 | AGACCCTGTCTCAAG[-/A]AAAAAAAAAAAAAAA | 57630 |
| rs780774741 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253440 | TAGAGAGCCCATGGG[C/T]TTTTGTCATGTTTCA | 57630 |
| rs780806564 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147177 | TATGTTTCCATTACA[-/T]TATTTGTTCACTGAA | 57630 |
| rs780818850 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169164261 | GTGAAAAACTTCTTG[C/T]TGAATAAATTAATGA | 57630 |
| rs780821043 | snp | C/T | 3.29609e-05 | 0.00405948 | missense | SH3RF1 | GRCh38.p7 | 4:169117631 | CTGATACCACAGCTG[C/T]GGGGACAACACTGGG | 57630 |
| rs780827405 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169229160 | AGGATCTTGTTCTGC[A/G]GCCCAGGCTGGAGTG | 57630 |
| rs780833748 | snp | A/G | 3.31246e-05 | 0.00406955 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169269123 | TCGCTTGCAAAACGT[A/G]TGCTGGCAAGGCAAG | 57630 |
| rs780863634 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169230141 | ACCCAGGGGCGGAGG[C/G]TGCAGTGAGCCAAGA | 57630 |
| rs780875863 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104350 | AAACAAGTAACTGGA[C/T]CAACTCCAGGGACAG | 57630 |
| rs780879392 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169266215 | TGATAACATTCAATA[C/T]ACTTTGGCTAAACGC | 57630 |
| rs780886949 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130768 | GTCTTATCCATGATA[C/T]AACCCAAGATTAATT | 57630 |
| rs780929961 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169184346 | GTGCACACATCCAAA[C/T]AGATCTCAGCTTCCA | 57630 |
| rs780973419 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169132742 | CTTTCCCTGAGGCCA[A/C]TGAATACAAAGATGC | 57630 |
| rs780974770 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116142 | GCATAGTGACTCACA[C/T]GTAGGGAGCACCTGA | 57630 |
| rs780979211 | snp | A/G | | | stop-lost | SH3RF1 | GRCh38.p7 | 4:169096521 | AGTGTCAGTCTCCTC[A/G]TATGTTTTCCACAAA | 57630 |
| rs780994437 | snp | A/G | 1.66103e-05 | 0.00288182 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130182 | AAGAAAAGTTATTAA[A/G]AAGAAGACTATGTTT | 57630 |
| rs781004444 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147193 | TATTTGTTCACTGAA[G/T]GCACACCATAAATCA | 57630 |
| rs781041442 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220070 | AAAGAAATACCAAAA[C/T]TGTTTCCAATCAGTC | 57630 |
| rs781047704 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224570 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 57630 |
| rs781069194 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100967 | TCTCTCAAAGCCTGG[C/G]TCCAGTTCTCCCCTG | 57630 |
| rs781070766 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169100404 | TAGAGTGCAATGGCA[C/T]GATCTCAGCTCACCA | 57630 |
| rs781084779 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125109 | AATGGGAAATGGTCA[C/T]ATTTTGCCATGTCCA | 57630 |
| rs781119676 | in-del | -/TCAACATATGAAAT | 1.7921e-05 | 0.00299335 | splice-acceptor-variant | SH3RF1 | GRCh38.p7 | 4:169136621 | GCAGCCGAGTTAAAC[-/TCAACATATGAAAT]TGCAAAAGCAACCAA | 57630 |
| rs781123178 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175199 | TCAGTCCACTTCTGA[A/C]AATTTCTACTGCTAC | 57630 |
| rs781130323 | snp | A/G | 1.89979e-05 | 0.00308198 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169107224 | GAAAAAAAAAATAAT[A/G]AGCCTTAGTTGGAGA | 57630 |
| rs781170065 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169204552 | TATATTACCTTCTCT[-/T]TTTTTTTTTTTTTTT | 57630 |
| rs781209656 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169176278 | ATGGATCTGTCATGT[A/G]CCCCCCAAGCTCTGG | 57630 |
| rs781227695 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169222224 | ATCCTAGCACTTTGG[C/G]AGGCCGAGGCAGGTA | 57630 |
| rs781229444 | in-del | -/CAAGT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169190923 | ATGGTTTAACACACA[-/CAAGT]CAATAAATGTGATAC | 57630 |
| rs781240373 | in-del | -/TGTGTGTGTGTGTG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169187521 | CAACGAATTTCTGTG[-/TGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 57630 |
| rs781263267 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169259988 | TATTGTCTTGGGTTT[-/G]GCTTAAACTACATTA | 57630 |
| rs781311050 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169215690 | TTTCATTATATTTCT[C/T]TCAGAAACATCAAAT | 57630 |
| rs781326875 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180506 | GGTCTTCAAAGCAAA[A/G]GTGCGGAAAGAAAAG | 57630 |
| rs781333281 | snp | C/G | 1.9969e-05 | 0.00315977 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169122213 | GCCTGGTGGTGTGGA[C/G]GCAAGGACAGTGGCA | 57630 |
| rs781337381 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169246415 | ACTGAGCTAGGAGTA[C/T]GTGCAACCCCGCTCA | 57630 |
| rs781340638 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227620 | CTGGGGTGTTCCATA[A/G]CATCTATGCATTATT | 57630 |
| rs781362940 | in-del | -/CAGCATTGCGGGCCTG | 3.71368e-05 | 0.00430894 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169116633 | TGTGCGCTGCAACTA[-/CAGCATTGCGGGCCTG]GTAGATGGGAAGAGG | 57630 |
| rs781370464 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169150103 | ACACACTCTATCCAT[A/G]GCCAGAGAAATGTCT | 57630 |
| rs781371402 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169134276 | AGCCTTGTTTCCTAA[C/G]CTACTTGAACCAAAA | 57630 |
| rs781418551 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167208 | GAAAAGAAGATGTTT[G/T]TATAGCCATGGAAGG | 57630 |
| rs781428200 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169214213 | CGAGATCTGGCTGTT[C/T]AAAAGTGTGTGGCAC | 57630 |
| rs781459008 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169120085 | CTGTCCTATGCATAG[C/G]ATGTTTCACTCTTAG | 57630 |
| rs781459786 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192770 | TAAAGAAGCTGTTTC[-/AT]ATATATATATACATA | 57630 |
| rs781485802 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154852 | CTATGAATTGTAACT[C/T]CTTTATGTTCAGCTT | 57630 |
| rs781494656 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206588 | TGAAGTCAAGAAACA[C/T]TTGGGACAAGTGCTT | 57630 |
| rs781496114 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169125475 | TCTGGCTAAAGAGAG[A/G]GGAAGTAGTCCAGTA | 57630 |
| rs781512629 | snp | A/G | 1.72178e-05 | 0.00293404 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156694 | CCTTTAAAAAAAAAA[A/G]AGGGATGAATTTTAA | 57630 |
| rs781544674 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169263275 | CTACAAAAAAGAACC[C/T]CATCATAGATAGAGA | 57630 |
| rs781559968 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249667 | AAGGATCCAATCCCC[A/C]CGTTGGAGACACACA | 57630 |
| rs781580538 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192655 | CTACCCAAAGGAAAA[G/T]AAGTCATTATATGAA | 57630 |
| rs781584115 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169126943 | TTGGCCATGAGTGGT[A/G]TTTACCTTTATTGAC | 57630 |
| rs781611271 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226427 | ACTACCATTCCACAG[C/T]AGTGAAAAGCAAAAT | 57630 |
| rs781634341 | snp | G/T | 1.64784e-05 | 0.00287035 | stop-gained | SH3RF1 | GRCh38.p7 | 4:169156557 | ATTGACTTCCCCATG[G/T]TACCAATTTTCATCC | 57630 |
| rs781642004 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169237269 | GAAAGTCATACTTAG[A/G]CTCATGGATTATTTT | 57630 |
| rs781643243 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166265 | AAGTTCTTTCCCATC[C/T]TGCCAGATGGTGGTG | 57630 |
| rs781653723 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169111716 | AGTATGTCCAGATAA[A/G]GTTGTTATACTGATG | 57630 |
| rs781659604 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169113181 | AGTGGTGTGATCTCG[G/T]CTCACTGCAACCTCC | 57630 |
| rs781681149 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169191414 | ACAAACAAATGGAAA[C/T]ACATCCCATGCTCAT | 57630 |
| rs781706966 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258997 | ACTTACATTGCTACG[A/G]TATTATTTTGGGGTA | 57630 |
| rs781709539 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238285 | ACTCCGCACAGCAGG[C/G]AGAAAGGAACTACCT | 57630 |
| rs781735533 | snp | C/T | 1.68832e-05 | 0.00290539 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106951 | GTCCAGGGAACTTGC[C/T]TTCCTATGAAAAGCA | 57630 |
| rs781752630 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211032 | ATGCTCTCAAAAAAC[C/G]TCACTTCCTCAAAAC | 57630 |
| rs781778088 | snp | C/T | 1.78353e-05 | 0.00298619 | synonymous-codon | SH3RF1 | GRCh38.p7 | 4:169106870 | AACGACAGGTCTAGA[C/T]TCATTCAAGACAGGA | 57630 |
| rs781778879 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169238111 | TTGCTGTATTCAGAA[C/T]AGAGCCCTATCTCTG | 57630 |
| rs781779639 | snp | C/T | | | upstream-variant-2KB | SH3RF1 | GRCh38.p7 | 4:169271246 | GGGGCGGGATTGGGG[C/T]GGCGGCCTGAGGGGG | 57630 |
| rs796065501 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192922 | ATCATATATATGTGA[-/TA]TATATATATATGATG | 57630 |
| rs796067419 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169156317 | ACTTGTATTTTTTTT[-/T]GCAAAAGGCAACACG | 57630 |
| rs796116182 | snp | A/T | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094429 | ATAGAAAACCCATAC[A/T]TTATATTACCTAATG | 57630 |
| rs796126195 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130245 | AAGGCAAGTCACATT[-/A]AAAAAAAAAATCTGT | 57630 |
| rs796198128 | in-del | -/AG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198357 | ACAGTCTACAAATAG[-/AG]TGTTAAATCAGCAGA | 57630 |
| rs796239055 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218643 | AGGGACCAAAAGTGA[A/G]CACCACCATCTCAAT | 57630 |
| rs796244003 | snp | C/T | | | missense | SH3RF1 | GRCh38.p7 | 4:169117589 | GCAACAAGACCTTAG[C/T]CTGAGGACTTGTCTG | 57630 |
| rs796245864 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239073 | TCTGGGTCAATTCTT[A/C]AATATACTAGAATAT | 57630 |
| rs796339069 | in-del | -/AGAG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169256330 | AAGGGAGGGAGAAAT[-/AGAG]GGAGGGAGGGAGTAT | 57630 |
| rs796345779 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169148250 | AGAAGTCTAGGGAAG[C/T]GATGAACTGCAGAGT | 57630 |
| rs796381842 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242305 | ATACCACTTATGCAG[C/T]GACCCATGTTCTAAC | 57630 |
| rs796384055 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169157759 | TTTCTTTTTTTTTTT[-/T]AAGACGGAGTCTTGC | 57630 |
| rs796397557 | multinucleotide-polymorphism | GG/TT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166422 | AAATCCTATCCTTAT[GG/TT]GAGGAATTGGCAGAT | 57630 |
| rs796409020 | multinucleotide-polymorphism | CA/GG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124915 | TTCATTCACCCGGAG[CA/GG]GACCTGGAGTCCTGC | 57630 |
| rs796440958 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248261 | CATTAATGATAGACC[A/G]CATAAAGAAAATGTG | 57630 |
| rs796443229 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192317 | TCACTAATGATCAGG[C/G]AAATGCAAACATGAA | 57630 |
| rs796447929 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255613 | TACATACACACATAC[-/AT]ACACACATACACACA | 57630 |
| rs796469839 | in-del | -/TA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192932 | TGTGATATATATATA[-/TA]TGATGGAATACTACT | 57630 |
| rs796470515 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169130709 | AATTACTTATAAAAT[A/C]TTTAAAGGAACAATG | 57630 |
| rs796533900 | in-del | -/AAGCCC | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197634 | GTCTCAAAAAAAAAA[-/AAGCCC]AAAAAGCCCACCTTA | 57630 |
| rs796544462 | multinucleotide-polymorphism | ATC/GTA | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172355 | TTAAGAATATGCCCG[ATC/GTA]ATGGATATACCTGTA | 57630 |
| rs796580756 | in-del | -/GG | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169165645 | AAAAAGGCGGGGGGG[-/GG]AGTCAGGTAAGGCCT | 57630 |
| rs796592195 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169179972 | CAACAAGCTTTCTTG[A/G]AGGAAGGTGTGAATA | 57630 |
| rs796614956 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169178948 | AACTCCTGCCAAATG[C/T]TGGAAGTCCAGGGAA | 57630 |
| rs796635248 | multinucleotide-polymorphism | AA/TT | | | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094786 | CATTGTTTTTTTTTA[AA/TT]AAAAAGGTTAATTTA | 57630 |
| rs796660289 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226373 | CTTTTCATCACAGTT[C/G]TCGTGTCTACATATC | 57630 |
| rs796662406 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233525 | TTTCAAAGTGTTTTA[C/T]ATCTATTAACTCATT | 57630 |
| rs796666454 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169258452 | TTCAGACTTGTTTTA[C/T]AAAAATGAGTAGAAA | 57630 |
| rs796671083 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169194794 | AAAGTGATTGTATCA[A/G]TGCATGTTCCCTACC | 57630 |
| rs796722308 | in-del | -/AT | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169192933 | GTGATATATATATAT[-/AT]GATGGAATACTACTC | 57630 |
| rs796735719 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216675 | GTGAGACCCCCATCT[C/T]ACTCAAAAATCACTA | 57630 |
| rs796747521 | in-del | -/A | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169163113 | GAGAGAAAAAAAAAA[-/A]CAAACTAGAGATAAA | 57630 |
| rs796749332 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144987 | TTGCAAAGTTTCCCA[A/G]GCCAACCATCCAACC | 57630 |
| rs796757118 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169108020 | ATCTCTTGAATTTTT[A/G]TCTCTTGATACTTTC | 57630 |
| rs796759914 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208837 | CCAAGAAGTAGGAGT[A/G]GGCCTACGCAGAAAC | 57630 |
| rs796762720 | in-del | -/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169144761 | GGCAGGGTCAACTGA[-/T]TTTTTTTTTTTAAGG | 57630 |
| rs796778186 | snp | A/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169260890 | TTTATAATCTTTTCG[A/G]TATCTTTTCAGTAAC | 57630 |
| rs796797018 | snp | A/C | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169255624 | ATACATACACACATA[A/C]ACACACACACACACA | 57630 |
| rs796797159 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213093 | AAGAGTATGTTTCGT[C/T]TTGTAAGAGACTGCC | 57630 |
| rs796827531 | in-del | -/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169102393 | CAAAGATCATACATA[-/G]GATTTTTTTTTTTCC | 57630 |
| rs796839488 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185294 | CAAGAGAGAAACAGC[C/G]GTGGGAGGCAGTGAT | 57630 |
| rs796975354 | snp | A/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169141823 | TTTGCTTTTTTTTTT[A/T]TTTTTTTGAGATGGA | 57630 |
| rs796990606 | snp | C/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169147335 | ATGAACATGGAATTG[C/T]CATTAATTCTAAGTG | 57630 |