SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12725 | snp | C/T | 0.0198 | 0.0975087 | downstream-variant-500B, utr-variant-3-prime | RAD54L, LRRC41 | GRCh38.p7 | 1:46278710 | CTGAGGTCCTGGAGG[C/T]CTTGA | 10489 |
rs1048771 | snp | C/T | 0.268175 | 0.249345 | synonymous-codon, downstream-variant-500B | RAD54L, LRRC41 | GRCh38.p7 | 1:46278228 | TGCTGCCTCCACTGC[C/T]ATCACCTTCGTCTTC | 10489 |
rs1150065 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | LRRC41 | GRCh38.p7 | 1:46285027 | GCAGGGCTAGAGTTT[A/G]ACCTCACCACCTCAC | 10489 |
rs1258476 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | LRRC41 | GRCh38.p7 | 1:46283713 | catctcaaaaaaaaa[A/G]aaaaGTTTTCTCCTC | 10489 |
rs1547180 | snp | C/T | 0.393619 | 0.204631 | upstream-variant-2KB, intron-variant | UQCRH, LRRC41 | GRCh38.p7 | 1:46302736 | CCTCGGCCCCTGCCC[C/T]AGGGCAGCCGGGCCA | 10489 |
rs3208553 | snp | G/T | 0 | 0 | downstream-variant-500B, missense | RAD54L, LRRC41 | GRCh38.p7 | 1:46278921 | GCTACCTGCCATGTG[G/T]TTAGCGACTCATGGG | 10489 |
rs3215667 | in-del | -/C | | | upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46303474 | CTAAAATAGTAGCTC[-/C]TAAGAGACTTGGAAA | 10489 |
rs3753361 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | UQCRH, LRRC41 | GRCh38.p7 | 1:46302522 | AACGAAAGGGTCGGG[A/G]CGCCGCGGCCTGTCT | 10489 |
rs3753362 | snp | G/T | 0.302184 | 0.244493 | intron-variant | LRRC41 | GRCh38.p7 | 1:46301079 | GAGGAACTTCTTCCC[G/T]TGTGGCCTCTTCCCC | 10489 |
rs4660919 | snp | A/G | 0.46875 | 0.121031 | intron-variant | LRRC41 | GRCh38.p7 | 1:46288814 | AGCAGGACATTAAGA[A/G]CAGGAAAAACAATAC | 10489 |
rs6673740 | snp | C/T | 0.451109 | 0.148509 | intron-variant | LRRC41 | GRCh38.p7 | 1:46291620 | gctggagtgcaatgg[C/T]acaatcttggctcac | 10489 |
rs6676038 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | LRRC41 | GRCh38.p7 | 1:46295717 | TGCTGGTCAACTCTA[A/G]TGCTTGTGAAATACT | 10489 |
rs6676957 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46283561 | TGGGTCTGGAAGTTC[A/C]AGAGAAAGATCTGGG | 10489 |
rs6686393 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | LRRC41 | GRCh38.p7 | 1:46291621 | ctggagtgcaatggc[A/G]caatcttggctcact | 10489 |
rs6692339 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | LRRC41 | GRCh38.p7 | 1:46292588 | AAATAGGGATTTTAC[C/T]TTCTCACTTTTATCA | 10489 |
rs6697623 | snp | A/G | 0.221737 | 0.248397 | intron-variant | LRRC41 | GRCh38.p7 | 1:46291870 | cagccTAAATTTTCT[A/G]GGGAGGAGAGGGTct | 10489 |
rs10158050 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | LRRC41 | GRCh38.p7 | 1:46294170 | cccaggctggagtgc[A/G]atggtgtgatctcgg | 10489 |
rs10581963 | in-del | -/T | | | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46304388 | ATATGCACTAATTAA[-/T]TTTTTTTTTTTTTTT | 10489 |
rs10890387 | snp | A/G | 0.449979 | 0.150028 | intron-variant | LRRC41 | GRCh38.p7 | 1:46287355 | CCTCATGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 10489 |
rs10890388 | snp | C/T | 0.397813 | 0.201621 | intron-variant | LRRC41 | GRCh38.p7 | 1:46295824 | CTCTTCCTCATAAGG[C/T]CTGTTGTCCTCATTC | 10489 |
rs11211266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LRRC41 | GRCh38.p7 | 1:46287148 | gagtctcactctgtc[A/G]cccaggctggagtcc | 10489 |
rs11444271 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46305321 | AAAAAAAAAAAAAAA[-/AAA]CTAAAGAAAGAAATG | 10489 |
rs11542623 | snp | C/T | 0.263674 | 0.249632 | missense | LRRC41 | GRCh38.p7 | 1:46280492 | CCGAGGCCTTCAGAA[C/T]GGAGCACAGCAGTGG | 10489 |
rs11542624 | snp | A/C/T | 1.65792e-05 | 0.00287912 | missense | LRRC41 | GRCh38.p7 | 1:46286133 | GTGCCTGAGTCAGCC[A/C/T]TTTTCATCCTTATTC | 10489 |
rs11576358 | snp | C/G/T | 1.68821e-05 | 0.0029053 | intron-variant | LRRC41 | GRCh38.p7 | 1:46280571 | GTTTTCTGGATATGG[C/G/T]GGGGAAAGAAGATTC | 10489 |
rs11586007 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46304418 | tgagatggaatctcg[C/T]tctgtcgcccaggct | 10489 |
rs12065340 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | LRRC41 | GRCh38.p7 | 1:46293873 | ggttcaagcaattct[A/G]cctcagcctcccaag | 10489 |
rs12142240 | snp | C/T | 0.221737 | 0.248397 | intron-variant | LRRC41 | GRCh38.p7 | 1:46281629 | GGCAGAGTCACAAAA[C/T]TGAGAAGATACAATA | 10489 |
rs12402705 | snp | A/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46294904 | ggccACAATTTATTG[A/T]TTATACAAAAGTCAT | 10489 |
rs12411245 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | LRRC41 | GRCh38.p7 | 1:46283237 | AAGAGTAAGGAGTCC[A/G]GAGGAACTACTGAAA | 10489 |
rs12726268 | snp | G/T | 0 | 0 | intron-variant | LRRC41 | GRCh38.p7 | 1:46283491 | CAAGTTGGATGTAAT[G/T]AGTTGGGTGGGGTAT | 10489 |
rs12751177 | snp | C/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46283414 | acttgaggccaagag[C/T]tcgagaccagcccgg | 10489 |
rs13374005 | snp | A/G | 0.0237945 | 0.106447 | intron-variant | LRRC41 | GRCh38.p7 | 1:46285312 | ATTAGGCACACAGCT[A/G]GTGCTGCTAGGCAAT | 10489 |
rs13374933 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | LRRC41 | GRCh38.p7 | 1:46287092 | acaggtgtgagtcac[C/T]gcacctagccCCTTA | 10489 |
rs17102110 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | LRRC41 | GRCh38.p7 | 1:46281696 | GCACAGACAGTAGCA[G/T]TTCTCTGGATTTCTG | 10489 |
rs17413652 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | LRRC41 | GRCh38.p7 | 1:46301504 | CCCCTCCGCACACCG[A/G]CCGACTTCTAAAAGC | 10489 |
rs28363249 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B, utr-variant-3-prime | RAD54L, LRRC41 | GRCh38.p7 | 1:46278619 | GATGACCACTGTAAC[C/T]TCCTGGCCCAGGGTT | 10489 |
rs28363250 | snp | A/C/T | 1.68863e-05 | 0.00290566 | intron-variant, utr-variant-3-prime | LRRC41 | GRCh38.p7 | 1:46279378 | CCCAGCACAGAAATA[A/C/T]CTGTATTCCAACTCC | 10489 |
rs28363251 | snp | C/T | 4.95479e-05 | 0.0049771 | missense | LRRC41 | GRCh38.p7 | 1:46279578 | AGAAATTGGGCTGGG[C/T]GCTTCTCAAACAGAC | 10489 |
rs28363252 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | LRRC41 | GRCh38.p7 | 1:46279912 | AGTCTATGAGGGGAG[C/T]CTGGCACAGTACATT | 10489 |
rs28377715 | snp | G/T | 0 | 0 | intron-variant, downstream-variant-500B | LRRC41 | GRCh38.p7 | 1:46279094 | TTGGAACTGGTAGGG[G/T]GAGATGGATTAGATA | 10489 |
rs28910278 | snp | A/G | 0.0112446 | 0.0741341 | missense, downstream-variant-500B | RAD54L, LRRC41 | GRCh38.p7 | 1:46278251 | TCGTCTTCCACCAGC[A/G]TTCTCATGAGGAGCA | 10489 |
rs34077858 | in-del | -/G | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46301131 | CCAACCTGCTCCCCT[-/G]CTAGTTAGCCATCTC | 10489 |
rs34133032 | in-del | -/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46287215 | CGGGTTCACACCATT[-/T]CACCTGCCTCAGCCT | 10489 |
rs34185697 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46304402 | ATTTTTTTTTTTTTT[-/TT]GAGATGGAATCTCGC | 10489 |
rs34412540 | in-del | -/T | 0 | 0 | intron-variant | LRRC41 | GRCh38.p7 | 1:46283723 | CTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 10489 |
rs34555094 | in-del | -/C | | | frameshift-variant | LRRC41 | GRCh38.p7 | 1:46285671 | AGCACCCTTCTTCCC[-/C]TGCAGCTCGCTTGAA | 10489 |
rs34782546 | in-del | -/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46295962 | GACATTAGCTTTTTT[-/T]CCACCTGTTATTTGG | 10489 |
rs35013913 | in-del | -/T | | | frameshift-variant | LRRC41 | GRCh38.p7 | 1:46298349 | GAGGTAGGATGCTTT[-/T]GAAGTATTGGGCCTG | 10489 |
rs35278560 | in-del | -/C | | | upstream-variant-2KB, intron-variant | UQCRH, LRRC41 | GRCh38.p7 | 1:46302252 | GCAGCCCGGCAGTCC[-/C]GGGATCCCCGGGCCG | 10489 |
rs35564317 | in-del | -/C | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46301393 | GGACTTTTCTGAGCT[-/C]CCCTGCTCAGCTCTA | 10489 |
rs35723042 | in-del | -/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46293420 | AACTTTTGTATTTTT[-/T]GTAGAGACAAGGTGT | 10489 |
rs35912501 | in-del | -/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46284464 | CAGTATATAAAAATT[-/T]AGTTTGAGAAACAAG | 10489 |
rs55906839 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | LRRC41 | GRCh38.p7 | 1:46295845 | GTCCTCATTCTGAAC[A/G]CCAAGGGTTGCAGTC | 10489 |
rs56306320 | snp | G/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46292100 | GGGTGGATCACTTGA[G/T]GTCAGGAGTTCGAGA | 10489 |
rs56351724 | snp | A/G | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46292080 | GCACTTTGGGAGGCC[A/G]AGGTGGGTGGATCAC | 10489 |
rs57551061 | snp | A/C | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46293100 | GAGGCAGGAGAATCA[A/C]TTGAACCCGGGAGGC | 10489 |
rs57641382 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46282212 | GAAAGGCAAAGGGAT[A/G]GTTTAACCTAGACGC | 10489 |
rs57732544 | in-del | -/AAAAT/AAAATAAAAT | 0.5 | 0 | intron-variant | LRRC41 | GRCh38.p7 | 1:46299907 | AAAATAAAATAAAAT[-/AAAAT/AAAATAAAAT]GGAGATAACAGTAAT | 10489 |
rs58227852 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46299552 | ACCACTGCACTCCAG[C/T]CTGGATGACAGAGCA | 10489 |
rs58864979 | snp | A/G | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46281733 | GAGTAGTTTTCTGAA[A/G]AAACTGGCCTTGAAG | 10489 |
rs58924829 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LRRC41 | GRCh38.p7 | 1:46294399 | AGGTGTGAGCTACCG[C/T]GCCCAGCCCTTTCTT | 10489 |
rs59245920 | snp | C/T | | | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46304290 | AAAGAATGTACGATG[C/T]GATTCTGTGATGGAA | 10489 |
rs59632701 | in-del | -/A | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46283040 | AAAAAAAAAAAAAAA[-/A]GATACAACTATAGAG | 10489 |
rs59951286 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | LRRC41 | GRCh38.p7 | 1:46281690 | TGACAGGCACAGACA[A/G]TAGCAGTTCTCTGGA | 10489 |
rs60249294 | in-del | -/T | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46294612 | TTTTTTTTTTTTTTT[-/T]GAGTCGGAGTCTTGC | 10489 |
rs60486184 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | LRRC41 | GRCh38.p7 | 1:46299624 | GTTCACACCTGTAAT[A/C]CCAGCACTTTGGGAG | 10489 |
rs60791711 | in-del | -/A | | | intron-variant | LRRC41 | GRCh38.p7 | 1:46282092 | AAAAAAAAAAAAAAA[-/A]TCACAGCTAGGAGAG | 10489 |
rs60968329 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46294559 | GTCAGTCACTGTACC[C/T]GACTCTTGTGCCTTT | 10489 |
rs61274010 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | LRRC41 | GRCh38.p7 | 1:46284123 | TATAAGAGGCTGGAA[A/G]GGGCTGTGAGTAAGA | 10489 |
rs61784600 | snp | C/T | 0.00578954 | 0.0534907 | intron-variant | LRRC41 | GRCh38.p7 | 1:46281417 | ATTAAGTCAGAACCA[C/T]GTGGGAGTGTCAGCA | 10489 |
rs71062750 | in-del | -/AA | 0 | 0 | intron-variant | LRRC41 | GRCh38.p7 | 1:46290944 | GAGCAGGAATGTCTT[-/AA]AAAAAAAAAAAAAAA | 10489 |
rs71497584 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | LRRC41 | GRCh38.p7 | 1:46291620 | GCTGGAGTGCAATGG[CA/TG]CAATCTTGGCTCACT | 10489 |
rs72677576 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | LRRC41 | GRCh38.p7 | 1:46289483 | TAAGAATCTATGGGC[C/T]GGGCGCGGTGGCTCA | 10489 |
rs72883403 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46293228 | TCCTGAGATTAGGAT[C/G]GTCACTTTTATTATT | 10489 |
rs72883410 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46294983 | TAACCAATTGCTAGA[A/G]AATAATTTATTGGGT | 10489 |
rs72883412 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46295548 | CAAAAGTGGGAAGCG[A/G]AAAGACACCCTCTGG | 10489 |
rs72883414 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46296011 | GCCCAGTTCAAATAC[C/T]ACTTCCTAGGAAAGA | 10489 |
rs72883415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LRRC41 | GRCh38.p7 | 1:46296605 | CTTAAATGAGAGCTC[C/T]AGTGATTTATATCTG | 10489 |
rs72883416 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46297372 | TGTGTCCCCTGCAAA[C/T]ACAGTGAGCAAGCAA | 10489 |
rs72883417 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46297463 | AAATCCATTCCATCA[C/T]TGCCTCTGCACTTTA | 10489 |
rs72883418 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46297871 | GTAAAATGTTAATAA[C/T]AGCTATTTCATAGGG | 10489 |
rs72883420 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46297918 | GGTAAATGAGTTTCT[C/G]TGGGTAAAGTGCCTA | 10489 |
rs72883422 | snp | A/C/G/T | 0.0268034 | 0.112722 | intron-variant | LRRC41 | GRCh38.p7 | 1:46298221 | GGGGTAATATTTACC[A/C/G/T]GAAGAACATTATGGT | 10489 |
rs72883423 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | LRRC41 | GRCh38.p7 | 1:46298588 | AGGGGCAAGGGTGAG[A/T]TCATCCCACAAAACA | 10489 |
rs72883424 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46300490 | CGGGCTGAATGAAAG[C/T]GTTAATTCCCTATGC | 10489 |
rs72883425 | snp | G/T | 0.0256215 | 0.110247 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | UQCRH, LRRC41 | GRCh38.p7 | 1:46302986 | AGTCACAAAATTCAT[G/T]CTCCGATCCTACGAG | 10489 |
rs72883426 | snp | G/T | 0.0256215 | 0.110247 | upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46303429 | AAGAATGTGAATTAT[G/T]CTAAAGAAATTTCGA | 10489 |
rs72883427 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46304192 | TCAGGTTAGGAATCC[C/T]TACCACATCTTCTAT | 10489 |
rs72883429 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | UQCRH, LRRC41 | GRCh38.p7 | 1:46304331 | TTTCCCAGAGAAAGA[A/G]TGCTGCTATAATTAT | 10489 |
rs72901066 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46279823 | AGAAGGTTCTCTGCA[C/T]GGACAATTCTCCATT | 10489 |
rs72901071 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46284517 | TTGTTTCTCAAACTG[A/G]TAATTTTTATATACT | 10489 |
rs72901074 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LRRC41 | GRCh38.p7 | 1:46288831 | AGGAAAAACAATACC[C/T]GGCAACCAAATCTCT | 10489 |
rs72901075 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46289006 | GTCAGATGGTTATTA[A/C]AATATCTGTGCCTAA | 10489 |
rs72901076 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | LRRC41 | GRCh38.p7 | 1:46289043 | GACAAAGATGGTGAG[C/T]CAAGATATTGTGGCT | 10489 |
rs72901077 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46289739 | GCACTCCAGCCTGGG[C/T]GATAGAGCAAGACTC | 10489 |
rs72901078 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LRRC41 | GRCh38.p7 | 1:46290531 | AACATACCATGTATT[C/T]AAATATTTTTAGAAT | 10489 |
rs74227093 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | LRRC41 | GRCh38.p7 | 1:46282147 | CTTGTTTGGCTACAT[A/G]AGGCTCAGGAAACAG | 10489 |
rs74227094 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LRRC41 | GRCh38.p7 | 1:46287904 | CCAAGGCAACAGTTA[C/T]TTATTTTGACGGATA | 10489 |
rs74558578 | snp | A/G | 0 | 0 | intron-variant | LRRC41 | GRCh38.p7 | 1:46289771 | GTCTCCAAAAAAAAA[A/G]GGAGTCTATGCTAAA | 10489 |