| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs190981365 | snp | A/G | 0.00117534 | 0.0242134 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362413 | GGGGTGCATGAGCCC[A/G]TGGGTCTGGCCTCTG | 267 |
| rs191010657 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56363209 | ACATCCAGCCCCCAA[A/C]AGATGGGCGCAAATT | 267 |
| rs191065406 | snp | A/G | 0.139564 | 0.224285 | intron-variant | AMFR | GRCh38.p7 | 16:56398232 | ATATATAACTCTATC[A/G]TTTATATATGTAACT | 267 |
| rs191171905 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56384576 | AACAATGGTGAAACA[C/T]GTTTCTCCATCATTG | 267 |
| rs191216281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423867 | AGCCCACAGAGTCCA[C/T]AAATCCCACCGCTTC | 267 |
| rs191243573 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56372752 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 267 |
| rs191245436 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56410290 | AAAAGATTAGACTTT[A/G]TAAAAAAAATTCTTC | 267 |
| rs191248857 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56385689 | ACAGAGTGAACCTAG[C/T]AGTGTTCAGAAAAGG | 267 |
| rs191304514 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56418440 | ACCCGGGAGGCGTAG[A/G]TTGCAGTGAGCCGAG | 267 |
| rs191456806 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56402394 | TCGGAGACCATATCC[A/G]GACAAATCAGAGGAG | 267 |
| rs191534614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410535 | AATATACCGTTTCAA[G/T]GGCTAAAGATGGACA | 267 |
| rs191557987 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56373324 | TGATCAAAGCTGCAC[C/T]GACCGGAGGGAACTC | 267 |
| rs191563805 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56375833 | GGAGGTCGAGAAGGG[A/C]AGATCACTTGAGGTC | 267 |
| rs191578008 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56413607 | TGGCGTAATTCTTCA[C/T]TGAAAGCATCCCCTG | 267 |
| rs191680945 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56390196 | TGAGATCAGTCCCAA[C/T]TCTCCCTCTAACTAG | 267 |
| rs191692553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56369435 | TGTGGCATCATGCCC[C/T]GAAAACACAGGTAAG | 267 |
| rs191697065 | snp | A/G | 0.0003704 | 0.0136038 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364103 | CAGTGGCACACGCTC[A/G]GTCTGGACACGGGGC | 267 |
| rs191732571 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56397568 | AGCATTAGGAGATAT[A/G]CCTAATGTAAATGAC | 267 |
| rs191986315 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | AMFR | GRCh38.p7 | 16:56393851 | ACTCAGCTCTGCACC[A/C]AGCAGACCTAATAGA | 267 |
| rs192005302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380000 | TAGCTCCATTAGGCG[A/G]TGCCCTAGCAGGCAT | 267 |
| rs192031483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407066 | TTTATATTAGGACTA[C/T]TGTATTTTAATTACA | 267 |
| rs192037864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390659 | CAAATAAATGATTTT[C/T]TTAAGTCCAATTCTC | 267 |
| rs192250829 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56381798 | CCAATCCTATAGAGG[A/G]AACACAAATGTAAAT | 267 |
| rs192255815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421228 | CCGCCTCTCAAACTG[C/T]TGAGACTGCCGGTGT | 267 |
| rs192341911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410020 | CAAAAAAAAAAATAC[A/G]AAAATTAGCTGGGAA | 267 |
| rs192359664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56372072 | TATATCAGAGACTTG[A/G]GCATTCATGGATTTT | 267 |
| rs192399902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56416500 | GCCCAAACTAAAGCA[C/T]AATGGTGCAATCTCC | 267 |
| rs192405308 | snp | A/G | 0.139225 | 0.224118 | intron-variant | AMFR | GRCh38.p7 | 16:56398081 | ATATATAAATGTATC[A/G]TTTATAATATATAAA | 267 |
| rs192432688 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56377863 | TATGCTTTATATTAG[C/T]GCCCACAAAACAAAA | 267 |
| rs192437188 | snp | C/G/T | 0.00214339 | 0.0326669 | intron-variant | AMFR | GRCh38.p7 | 16:56369146 | TACAGTATTCAATCT[C/G/T]TGTGAAGATAGAACC | 267 |
| rs192527263 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398695 | CTTATGAGATGCAGC[A/G]GAAGCAATGCTCAGA | 267 |
| rs192534720 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56419670 | ATGGTGGTGCACACC[C/T]GTAATCTCAGCTACT | 267 |
| rs192553584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380735 | TTGCTAAAACATGAC[A/C]AGAGTCACCCTTGCT | 267 |
| rs192657450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399539 | CTAAGTGAAAGAGGC[C/T]AGTCACAAAAAGTCA | 267 |
| rs192698641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56365005 | GTGCCTGACCATCTG[C/T]GCTGCTCATGCTCCC | 267 |
| rs192794177 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426014 | ATGAACCTGATTTAG[C/T]GGGAAATAAAAATGT | 267 |
| rs192866690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415701 | ACAACCAGGAACAAA[C/T]GCCCAAACTAGTTGC | 267 |
| rs192890195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377700 | TGACATGCTCACCTA[C/T]GTAGAAAATCTGGAA | 267 |
| rs192925182 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56405108 | GGTTTAACCATGTTG[A/T]AATTTAGTCCGATTT | 267 |
| rs192925364 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56376983 | AAGTTGTATAGATAA[C/T]TAATAATCTTCCACA | 267 |
| rs193049091 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56404774 | AGGGAGGGTTTGCAG[C/T]CACATTCATTTTTAG | 267 |
| rs193093538 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56397758 | AATGTATCATTTATA[A/G]TATATAAATGTATCA | 267 |
| rs193100964 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395530 | TCATGGGAAGTATCT[A/C]AAAATAATAAGAGCT | 267 |
| rs193225421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56388675 | CTATAAGAGTTTTTC[C/T]ATTTCTAAAAGTTTT | 267 |
| rs193228156 | snp | A/T | 0.0107246 | 0.0724382 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425699 | CAGCATCATCCGCCG[A/T]CCGCACCACGGCTTG | 267 |
| rs193254177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373715 | CATGCAGGAACAGAC[A/G]GGCAGCATGAGCAGG | 267 |
| rs193299496 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56410867 | AGCCTGGGCAACAGA[C/G]CAAGACTCTGTCTCA | 267 |
| rs199507277 | snp | C/T | 1.65277e-05 | 0.00287464 | synonymous-codon, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56414336 | ACAGCAAGCGGTATT[C/T]ACTAGAACCTGTAAA | 267 |
| rs199784409 | snp | A/G | 0.000376822 | 0.0137211 | missense | AMFR | GRCh38.p7 | 16:56362913 | GCAAGGGAGCGCTAG[A/G]AGGTCTGCTGCTTCT | 267 |
| rs199792465 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417192 | AGGTGGGGGGATTGC[C/T]TGAACTCAGGAGTTC | 267 |
| rs199826872 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421113 | TATAATGGTGACTAA[-/T]TTTTTTTTTTTTTTT | 267 |
| rs199850428 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56389900 | CTCACTTATCTGGCA[-/C]CAAACTTACTAAGAC | 267 |
| rs199862014 | snp | C/T | 3.33201e-05 | 0.00408156 | intron-variant | AMFR | GRCh38.p7 | 16:56369360 | CAGAGTCCACAGAAA[C/T]GTTCACTGTTAACAG | 267 |
| rs199947038 | snp | C/T | 0.00199098 | 0.0314885 | intron-variant | AMFR | GRCh38.p7 | 16:56369155 | CAATCTTTGTGAAGA[C/T]AGAACCCATTTATCA | 267 |
| rs200050790 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374426 | AAAAAAAAAAAAACA[A/C]TACATCAAATTCATC | 267 |
| rs200052611 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56365810 | CAGAGGGAGAGTGGA[G/T]CTGACAAGCTTACTG | 267 |
| rs200100657 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56410774 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAT | 267 |
| rs200174342 | in-del | -/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361535 | AATTAAAAAAAAAAA[-/T]CACAGAAATTTACTA | 267 |
| rs200259295 | snp | A/G | 1.64991e-05 | 0.00287215 | stop-gained | AMFR | GRCh38.p7 | 16:56401773 | GTTTCCGCGCAGCCT[A/G]CATGGAGTCCCAACA | 267 |
| rs200261942 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397832 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
| rs200262479 | in-del | -/CA | 0.0217236 | 0.101931 | intron-variant | AMFR | GRCh38.p7 | 16:56392979 | AAAGGTCGGGTTACC[-/CA]CACAAAGGGAAGCCC | 267 |
| rs200303524 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397810 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
| rs200320761 | snp | C/T | 0.000252417 | 0.0112314 | missense | AMFR | GRCh38.p7 | 16:56362964 | GCAGCCAGCATCCTT[C/T]GACGCAGGGTCACGG | 267 |
| rs200321273 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394896 | TCAGAGAATATTATA[A/T]ACACCTCTATGCAAA | 267 |
| rs200350064 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56406552 | AGTGACACCTTGTCT[A/C]AAAAAAAAAAAAAAA | 267 |
| rs200380370 | snp | C/T | 0.000135391 | 0.00822662 | missense | AMFR | GRCh38.p7 | 16:56385965 | GTAATGCCAAGAATG[C/T]TGGTGGTGTGCATCA | 267 |
| rs200534071 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390880 | AGTACAACTAGTTAG[A/T]TATAGTTTTCTGTTT | 267 |
| rs200560220 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56401440 | TTAAATCTTACAGGC[A/G]TATTTGCTATACTTC | 267 |
| rs200593665 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | AMFR | GRCh38.p7 | 16:56395079 | GACCAGACGGATTCA[C/G]AGCCGAATTCTACCA | 267 |
| rs200602035 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56421398 | GTTTTACAACCCTTT[-/A]AAAATATAAAAACCA | 267 |
| rs200721120 | snp | C/G | 3.30256e-05 | 0.00406346 | missense | AMFR | GRCh38.p7 | 16:56409443 | TCAAATCGATCCTTG[C/G]AGAGCTGAACCATCA | 267 |
| rs200814099 | in-del | -/GCAGGTAACAG | | | intron-variant | AMFR | GRCh38.p7 | 16:56418959 | TTCTGGAAGAGAGAA[-/GCAGGTAACAG]GGAGAGAGAGAGATC | 267 |
| rs200831992 | snp | A/G | 0.000197941 | 0.00994643 | intron-variant | AMFR | GRCh38.p7 | 16:56367548 | AGAGAAACAGTACCA[A/G]AAACAGTCCAGAGTC | 267 |
| rs200843944 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56398258 | AACTGTATCATTTAT[-/A]ATATGTAACTGTATC | 267 |
| rs200850337 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385633 | ATTTTTTTTTTTTTT[-/T]GGCTAAAATCGAAGG | 267 |
| rs200900867 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56404372 | ATTTTAATTCTCACC[A/G]TTATTAGATCACTGA | 267 |
| rs201017867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386058 | GTGTAAGTTTCAGAG[C/T]CCTGACTCTTTCCCC | 267 |
| rs201049182 | snp | C/T | 6.65591e-05 | 0.00576846 | intron-variant | AMFR | GRCh38.p7 | 16:56414370 | ATCAGAGAAAGGAAG[C/T]TTATTTCTTCCTGCT | 267 |
| rs201077400 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56384707 | ACATGCATACATACA[C/T]ACACACACACACACA | 267 |
| rs201099834 | snp | A/G | 0.000106986 | 0.00731312 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362249 | CACGGAAATCAAGCC[A/G]GCTTTGGACTGGAGG | 267 |
| rs201142255 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56410882 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 267 |
| rs201180102 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56379117 | TTTCTCATTGCTGAT[-/AA]AGATATATCCGAGAC | 267 |
| rs201184108 | snp | A/G | 7.01262e-05 | 0.005921 | missense | AMFR | GRCh38.p7 | 16:56364099 | GGTCCAGTGGCACAC[A/G]CTCGGTCTGGACACG | 267 |
| rs201202848 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403962 | TGAGGAAAAAAAATT[A/T]AAAAAAAGAAGATAA | 267 |
| rs201264142 | snp | A/G | 0.11228 | 0.208646 | intron-variant | AMFR | GRCh38.p7 | 16:56397773 | ATATATAAATGTATC[A/G]TTTATAATATATAAA | 267 |
| rs201274019 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394941 | TAGAAGAAATGGATA[A/T]ATTCCTCGACACATA | 267 |
| rs201282575 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390896 | TATAGTTTTCTGTTT[A/T]AAAAAAAAAAAAAAT | 267 |
| rs201373259 | snp | C/T | 0.000329446 | 0.0128302 | missense | AMFR | GRCh38.p7 | 16:56403030 | TAGTTCTTGTGCCGA[C/T]GAATTCGACGTTGCA | 267 |
| rs201525089 | snp | C/T | 3.31472e-05 | 0.00407093 | intron-variant | AMFR | GRCh38.p7 | 16:56405178 | ATGAGTAGGCCTCCA[C/T]CACCTCCCTCCCCAA | 267 |
| rs201580995 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374414 | TAAAAAAAAAAAAAA[A/C]AAAAAAAAACACTAC | 267 |
| rs201593756 | snp | C/T | 4.9423e-05 | 0.00497082 | intron-variant | AMFR | GRCh38.p7 | 16:56367434 | ACTCTCACTAGAGTG[C/T]GGGTTTTACCTGAGC | 267 |
| rs201766283 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56394334 | CACATTCAAAAGCTA[A/G]CAGAAGGCAAGAAAT | 267 |
| rs201828464 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56396618 | CATTCAGGACATAGG[C/G]ATGGGCAAGGACTTC | 267 |
| rs201913673 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56407805 | CAAAAGCATTCAGTA[C/T]CAGTACCCAACACAC | 267 |
| rs201925729 | in-del | -/TTATT | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56405368 | GTTCAAGTTTACCCA[-/TTATT]TTATTTTCTCTGCTT | 267 |
| rs201930008 | snp | C/T | 0.000106786 | 0.00730628 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362259 | AAGCCGGCTTTGGAC[C/T]GGAGGCTCGGAAAGT | 267 |
| rs201931820 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | AMFR | GRCh38.p7 | 16:56414243 | TCCATCCTTTCAGTG[C/T]AGACTTACCTGTCTC | 267 |
| rs202005496 | snp | A/G | 0.000281231 | 0.0118548 | missense | AMFR | GRCh38.p7 | 16:56404928 | ATGTGAATATGGTGC[A/G]TGAGGTCCAGGGACA | 267 |
| rs202026496 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394885 | ACAAACTACCATCAG[A/T]GAATATTATAAACAC | 267 |
| rs202034412 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409749 | AAAAAAAAAAAAAAA[C/T]CAGCCATCTGAAGAA | 267 |
| rs202035395 | in-del | -/A | 0.213333 | 0.247296 | intron-variant | AMFR | GRCh38.p7 | 16:56398611 | AAATATACAGATATT[-/A]AAAAAAAAAATCACT | 267 |
| rs202041168 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56410762 | TGGCACAAGCCTGTA[A/G]TCCCAGCTACTTGGG | 267 |
| rs202056433 | in-del | -/A | 0.0372196 | 0.131242 | intron-variant | AMFR | GRCh38.p7 | 16:56410579 | AAATTTTCACCACGC[-/A]AAAAAAAACATTATA | 267 |
| rs202067230 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56397751 | ATATATAAATGTATC[A/G]TTTATAATATATAAA | 267 |
| rs202074356 | snp | A/G/T | 0.000115389 | 0.0075948 | synonymous-codon, missense | AMFR | GRCh38.p7 | 16:56367527 | TGATGCTATCTGACC[A/G/T]CTGGAAGAGAAACAG | 267 |
| rs202121611 | snp | A/C | 1.65012e-05 | 0.00287234 | missense | AMFR | GRCh38.p7 | 16:56401774 | TTTCCGCGCAGCCTG[A/C]ATGGAGTCCCAACAG | 267 |
| rs202191766 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406118 | GAGGGGGGAGGGGAG[A/G]GGGGAGAGGGGAGAG | 267 |
| rs202204058 | snp | A/C | 0.000112429 | 0.00749679 | intron-variant | AMFR | GRCh38.p7 | 16:56385909 | TCTTAAAGCAGCTAG[A/C]AGACCTTACCATTGC | 267 |
| rs202221136 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56394956 | AATTCCTCGACACAT[A/G]CACCCTCCCAAGACT | 267 |
| rs367549659 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56381231 | AGACTTATTCACTAT[C/T]ACAAGAACAGCATGG | 267 |
| rs367557874 | snp | C/T | 4.94238e-05 | 0.00497086 | intron-variant | AMFR | GRCh38.p7 | 16:56367418 | ACAGCTCCATGAACT[C/T]ACTCTCACTAGAGTG | 267 |
| rs367621434 | snp | A/T | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56404983 | CTGTGTAATAGACAT[A/T]CGTCCCCTTTCCTTC | 267 |
| rs367643256 | snp | C/T | 0.000303628 | 0.0123175 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362449 | GTCTACATGCTTCCA[C/T]AACAACGACAGCAGT | 267 |
| rs367644947 | in-del | -/CATCTCATCTGAGATAAGGCAAGTCCCT | | | intron-variant | AMFR | GRCh38.p7 | 16:56379584 | ATAAGGCAAGTCCCT[-/CATCTCATCTGAGATAAGGCAAGTCCCT]AACGTCTATGAGCCT | 267 |
| rs367777283 | snp | A/G | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56408108 | CGGCGTGGTGGGCGA[A/G]AAGGAAAGCTGAAAT | 267 |
| rs367840761 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422917 | CTAAACTGTGCTCTA[A/G]AAAGATAAGTTTTGG | 267 |
| rs367849848 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56400325 | GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCTTG | 267 |
| rs367879014 | snp | A/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361935 | CTTCTCTGCTGAATT[A/T]AACCAGGAATAACAC | 267 |
| rs367945800 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56380696 | CAAATCTCTTAAGGC[A/G]GGGGCAACATGCTGC | 267 |
| rs367987913 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56406358 | GGCCGACTGCTTGAT[A/C]TCAGGAGTTCAAGAC | 267 |
| rs368011733 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | AMFR | GRCh38.p7 | 16:56396609 | AGGCAATACCATTCA[A/G]GACATAGGCATGGGC | 267 |
| rs368052748 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423834 | TCTCCATCAGAAGGA[C/G]CAGGAGACTTAATCT | 267 |
| rs368093883 | snp | A/G | 0.000712469 | 0.0188607 | intron-variant | AMFR | GRCh38.p7 | 16:56401685 | ACAAAGCACACACAC[A/G]CCCTGGACAGAACAC | 267 |
| rs368129270 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56423475 | CTGAAGAGATATTAA[-/CT]TTAGAATCTGAACAT | 267 |
| rs368147918 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | AMFR | GRCh38.p7 | 16:56409510 | ACATGACCACCTCTT[C/T]CACTGTCTGGACATT | 267 |
| rs368150926 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390768 | GCCTTCCAATAATGC[C/T]ACACTGTGACATACT | 267 |
| rs368219300 | snp | A/G | 4.94279e-05 | 0.00497107 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389306 | GACACGATTATTGTC[A/G]GCAATATTAAGAGAC | 267 |
| rs368502018 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383333 | CTCTTCCCTCTCCAC[C/T]GGCTGTCATGGCTCC | 267 |
| rs368538453 | snp | A/G | 1.78185e-05 | 0.00298478 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362495 | ACCCCACGACGTGGG[A/G]GCGGGCTCACACTGT | 267 |
| rs368604843 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56367286 | CCACGGGCACAGCCT[A/G]ATTTGCTACCCTTCA | 267 |
| rs368682412 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56396440 | AATGGGGAAAGGATT[C/T]CCTATTTAATAAATG | 267 |
| rs368713232 | snp | C/T | 1.70801e-05 | 0.00292229 | synonymous-codon | AMFR | GRCh38.p7 | 16:56362921 | GCGCTAGGAGGTCTG[C/T]TGCTTCTGAAGCCTC | 267 |
| rs368735628 | in-del | -/TTTTT | | | intron-variant | AMFR | GRCh38.p7 | 16:56419899 | TCACCAAATGCCTTT[-/TTTTT]CCAGTCTACACAAAA | 267 |
| rs368747246 | snp | C/G/T | 3.51854e-05 | 0.00419425 | intron-variant | AMFR | GRCh38.p7 | 16:56405255 | AGAGACTATAAAAAA[C/G/T]GATATTTTCTTTTTA | 267 |
| rs368757788 | snp | A/G | 1.66233e-05 | 0.00288295 | missense | AMFR | GRCh38.p7 | 16:56408052 | CAGCAGGAAAGCAGC[A/G]TGGCAACCAACAGGG | 267 |
| rs368791387 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383938 | TCTGAATGGCCTTCT[A/G]ATACTTTTACAAGAT | 267 |
| rs368876872 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56390947 | AGAAATCAAACTTTA[A/G]AGAGAAAACAGATCT | 267 |
| rs368887556 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387551 | GCTAACAAAATTCCA[A/G]GGATGCTTGTGTTAC | 267 |
| rs368928665 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56384299 | AGCAGTCACCTTATT[C/T]ATATTTATGACCTGT | 267 |
| rs368978217 | snp | C/G | 1.65392e-05 | 0.00287564 | intron-variant | AMFR | GRCh38.p7 | 16:56401709 | AGAACACCTGTCCCA[C/G]ATGGCCCTTCACAAA | 267 |
| rs368998160 | snp | A/G | 0.000329001 | 0.0128216 | synonymous-codon, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425321 | GCTCGAGGAAGAGCA[A/G]CGGCATGGCGGCAGC | 267 |
| rs369017257 | in-del | -/GT | | | intron-variant | AMFR | GRCh38.p7 | 16:56370694 | AGGGCTCTAGGGTGG[-/GT]GTGTGTGTAGGGAGA | 267 |
| rs369152492 | snp | G/T | 0.00186122 | 0.0304491 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362608 | AGCTGCCTGCTGCAG[G/T]CAGGCGACTGCTCAC | 267 |
| rs369160515 | snp | A/G | 1.65633e-05 | 0.00287774 | stop-gained | AMFR | GRCh38.p7 | 16:56363934 | ACTTGCGAGCTTGCT[A/G]GAGGAGTTCGTCCTT | 267 |
| rs369184945 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374112 | AGGTGGAGGTTGCAG[C/T]GAGCCGAGATCGTGC | 267 |
| rs369195034 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387748 | GAGGCAGAACATTTA[A/T]ATTTTATGGACAAAG | 267 |
| rs369390626 | snp | A/G/T | 0.000415614 | 0.0144097 | intron-variant | AMFR | GRCh38.p7 | 16:56414225 | AAAATCTAGTCACAA[A/G/T]AATCCATCCTTTCAG | 267 |
| rs369433667 | snp | A/G | 0.000116006 | 0.0076151 | synonymous-codon | AMFR | GRCh38.p7 | 16:56401840 | TGGAGTTGCAACTGC[A/G]AACCTGTGGAAACAA | 267 |
| rs369443221 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56410345 | CACTTGCCAGCCCAT[-/A]AATAAAGGCGGCATA | 267 |
| rs369445692 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379008 | CGCAAGATGATACAG[C/T]CACTCTGGAGGATGA | 267 |
| rs369454263 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56384550 | GACTAAGGTGGTTTG[C/T]ACTGGATTTCAACAA | 267 |
| rs369549246 | snp | C/T | 0.000159285 | 0.00892284 | synonymous-codon | AMFR | GRCh38.p7 | 16:56385997 | TTCAACCGAAAAACT[C/T]GGCAGCCAGCTCGCA | 267 |
| rs369604038 | snp | A/G | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56408005 | GCATTCCGTGGGTGT[A/G]GCCGGTGATGGAGCA | 267 |
| rs369623709 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367841 | CACCTAACTTCGGCA[C/T]GGCACCAAGGAAAAC | 267 |
| rs369886553 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395071 | AAGTCCAAGACCAGA[C/T]GGATTCACAGCCGAA | 267 |
| rs369902321 | snp | C/T | 0.000347939 | 0.0131852 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362767 | AAATTTATCAGCTGT[C/T]CAAACACTATAAGAC | 267 |
| rs369924336 | snp | A/G | 3.3557e-05 | 0.00409602 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389201 | ATCGAAATGGAAGAA[A/G]TGATTGTGTTGGTTT | 267 |
| rs369963180 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382097 | AGTAGCATTATTCAC[A/G]ATAGCTAAAATGTGG | 267 |
| rs369996822 | snp | A/C | 3.71906e-05 | 0.00431207 | intron-variant | AMFR | GRCh38.p7 | 16:56409599 | AGATGCTAAAAAAGA[A/C]AAATGTTTATGAAGG | 267 |
| rs370023605 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56365169 | CCTTCAGCTAAGCTC[A/G]AGAGGGAACTTCAAG | 267 |
| rs370077637 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56385451 | TGAAACCTCGTCTCT[A/G]CAAAAATTAGCCAGG | 267 |
| rs370112699 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56406997 | GTCAAGACGAAATAC[A/G]GTTGTATATTTTTCA | 267 |
| rs370139782 | in-del | -/GATA | | | intron-variant | AMFR | GRCh38.p7 | 16:56390879 | GAGTACAACTAGTTA[-/GATA]TAGTTTTCTGTTTAA | 267 |
| rs370148770 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56396307 | GCTACAGTAACCAAA[A/G]CAGCATGGTACTGGT | 267 |
| rs370219059 | snp | C/T | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56385921 | TAGCAGACCTTACCA[C/T]TGCATTGAGCTGGGA | 267 |
| rs370322822 | snp | A/G | 5.35662e-05 | 0.00517496 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362477 | AGTTTGATAACAGAT[A/G]TTACCCCACGACGTG | 267 |
| rs370482924 | snp | A/G | 0.000148259 | 0.00860858 | intron-variant | AMFR | GRCh38.p7 | 16:56367435 | CTCTCACTAGAGTGC[A/G]GGTTTTACCTGAGCA | 267 |
| rs370505650 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56405769 | GAGGCAGGAGGATTG[C/T]TCAAGCTTAGGAGTT | 267 |
| rs370508245 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56371741 | AGTGAGCCCTCAGTA[C/T]CACTATATAGGTGAG | 267 |
| rs370578661 | snp | A/G | 0.000199849 | 0.00999423 | intron-variant | AMFR | GRCh38.p7 | 16:56364114 | GCTCGGTCTGGACAC[A/G]GGGCAGGAAGCAAGG | 267 |
| rs370658978 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56396489 | AGCCATATGTAGAAA[A/G]CTGAAACTGGATCCC | 267 |
| rs370746686 | snp | C/T | 1.69522e-05 | 0.00291132 | missense | AMFR | GRCh38.p7 | 16:56364074 | AGCGTCTCCTCCAGG[C/T]GAGGACTGAGGTCCA | 267 |
| rs370810183 | snp | A/G | 0.00238307 | 0.0344362 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362407 | GGCTCAGGGGTGCAT[A/G]AGCCCGTGGGTCTGG | 267 |
| rs370847290 | snp | A/T | 1.64751e-05 | 0.00287007 | intron-variant | AMFR | GRCh38.p7 | 16:56402951 | AAAAACTAAAATGAG[A/T]AAACTTAGGCAACAT | 267 |
| rs370900989 | snp | A/C | 0.000279208 | 0.0118121 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362873 | CAGTCAGTCGGGCAC[A/C]GGGCGCAGGAGGCAG | 267 |
| rs370904126 | snp | A/G | 8.70693e-05 | 0.00659751 | intron-variant | AMFR | GRCh38.p7 | 16:56403159 | ACGGTAAAAGCGAAC[A/G]TGAACTTGCTAGTGA | 267 |
| rs370914847 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406196 | GACAAAATAAGTCTC[C/T]CATGGCTTTTTTTTT | 267 |
| rs370925520 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416438 | TTCTCAAACTCTTTA[A/G]ATAAAAGTCTATTTA | 267 |
| rs370971155 | snp | A/C | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425691 | CGGGCACCCAGCATC[A/C]TCCGCCGTCCGCACC | 267 |
| rs371039765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365034 | CCAGATGCAGACCTG[C/T]GCTGGCCAGGGTCAG | 267 |
| rs371060273 | in-del | -/GGC | | | intron-variant | AMFR | GRCh38.p7 | 16:56382535 | AAAAAAAAAAAAAAA[-/GGC]AAAAAAATCTCATAG | 267 |
| rs371130156 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56393344 | GTCATAATGACAGGA[A/T]CAAATTCACACATAA | 267 |
| rs371166041 | in-del | -/GAGTCGGGGAGGG | | | intron-variant | AMFR | GRCh38.p7 | 16:56370023 | GTAGGGAGGGGAGGG[-/GAGTCGGGGAGGG]CTGGAAAACTACCTA | 267 |
| rs371167798 | snp | A/G | | | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361443 | TTCCAGCCACACACA[A/G]CACACCAATAGAGTT | 267 |
| rs371190581 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383280 | CTTCCCTCCTGGAAA[C/T]CCAACTCCTCTGTGC | 267 |
| rs371195118 | snp | A/G | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56363036 | GCCGCATCATCTTCA[A/G]AACTTTTGTTCAAGA | 267 |
| rs371217450 | snp | A/G | 8.5465e-05 | 0.00653645 | missense | AMFR | GRCh38.p7 | 16:56363024 | AAGCTCTCTGAGGCC[A/G]CATCATCTTCAGAAC | 267 |
| rs371308420 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399117 | ACCATAATAAGAAAA[C/T]ACTTCACACCCACGA | 267 |
| rs371335169 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394604 | AAAAATTAGCCGGGC[G/T]CGGTGGCGGGCGCCT | 267 |
| rs371375873 | snp | C/T | 6.60077e-05 | 0.00574452 | synonymous-codon | AMFR | GRCh38.p7 | 16:56405005 | CTTTCCTTCCCACGT[C/T]CCTTCGTGGTTGAGG | 267 |
| rs371381439 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426966 | TCCCCAGGGCCTGTA[A/G]GAGTTCTCAGCCCAG | 267 |
| rs371383151 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | AMFR | GRCh38.p7 | 16:56401686 | CAAAGCACACACACG[A/C]CCTGGACAGAACACC | 267 |
| rs371411108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372915 | TGCTTGAACCTGGGA[G/T]GTGGAGGTTGCAGTG | 267 |
| rs371477726 | snp | A/C | | | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424003 | TGGGAACATGCAAGG[A/C]GACAAGATCCAAGAA | 267 |
| rs371511727 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56388607 | CTTGTAGTAACACTT[A/C]GCTTAAAATTCAAAC | 267 |
| rs371604189 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56404053 | TTTTTTTTTTTTTTT[G/T]GGACGGAGTGTCACC | 267 |
| rs371615978 | snp | C/G/T | 0.000204167 | 0.0101019 | intron-variant | AMFR | GRCh38.p7 | 16:56409375 | TTACACAATTCAAAG[C/G/T]TGGCAAACGTGGTGA | 267 |
| rs371675197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423638 | TTATAATCTTAACAT[A/G]GCAAAAACACTCTCC | 267 |
| rs371682856 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56396816 | ATCCAGAATCTACAA[A/T]GAACTCAAACTAATT | 267 |
| rs371752217 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374621 | AAAGACTCACCAACA[A/G]AGAATTCTATACCCC | 267 |
| rs371756918 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374233 | AATTCAAGGACTGTG[A/G]GACAACTACAAAAGG | 267 |
| rs371766807 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56372022 | CCCATCTTTTTTTTT[C/T]ACCTTAAACTATTAA | 267 |
| rs371818532 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380804 | CCTCAGCCTTGATTT[A/C]ATTGTCCATATCATT | 267 |
| rs371854854 | snp | A/G | 6.64308e-05 | 0.0057629 | intron-variant | AMFR | GRCh38.p7 | 16:56369179 | TTTATCATGCTTTAA[A/G]AGCCCAGTTTTACCT | 267 |
| rs371857108 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56406603 | GAAAAAAAGTCCTCT[G/T]AATCTAGTAGAATAA | 267 |
| rs371873000 | in-del | -/AAAC | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56376167 | AAGAACCACAAAGAG[-/AAAC]AAAATAGATTTGGAG | 267 |
| rs371891208 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427496 | TCCCATCACCCTTAG[A/G]AACAGGCTGCTGTTA | 267 |
| rs371895602 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406336 | AGCACTTTGGGAGGT[C/T]GAGGCAGGCCGACTG | 267 |
| rs371946593 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56394232 | GAGGGAAATTTATAG[A/C]ACTAAATGCTCACAA | 267 |
| rs371955674 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56384992 | TTTTTAGTAGAGACA[C/G]GGTTTCACTATATGG | 267 |
| rs371986194 | snp | C/T | 3.31868e-05 | 0.00407336 | intron-variant | AMFR | GRCh38.p7 | 16:56407923 | TTCCTTGAAAACAGA[C/T]AGAAATACAATCTGA | 267 |
| rs372051531 | snp | A/G | 0.00017751 | 0.0094193 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362567 | ACACCTGCATTTGTG[A/G]GACGTACGCATGAGG | 267 |
| rs372058533 | snp | A/G | | | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423755 | CTTCTTTAGGACTGT[A/G]AAGTTCAGCTTTACA | 267 |
| rs372077396 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56416892 | AATTAACATGGCTAA[C/T]CAGGAAAAAAAAAAA | 267 |
| rs372095095 | snp | A/G | 0.000131983 | 0.00812243 | missense | AMFR | GRCh38.p7 | 16:56401755 | AAAGATGTCCACAGG[A/G]CAGTTTCCGCGCAGC | 267 |
| rs372096570 | snp | C/T | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56409575 | ATAAAATTCCAAAAT[C/T]TGTCTTTGAGATGCT | 267 |
| rs372145806 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56409978 | TTTGAGATGAGCCTC[A/G]GTAACATGGGGAAAC | 267 |
| rs372160267 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56418979 | TAACAGGGAGAGAGA[C/G]AGATCTACTTTTCAC | 267 |
| rs372252237 | snp | A/G | 0.000124698 | 0.00789516 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362498 | CCACGACGTGGGGGC[A/G]GGCTCACACTGTGCG | 267 |
| rs372263452 | in-del | -/AC | 0.00119737 | 0.0244387 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425946 | GAAGAAAGAATATTA[-/AC]AGTCTTTCAAGTTTC | 267 |
| rs372393687 | snp | C/T | 0.00018543 | 0.00962708 | intron-variant | AMFR | GRCh38.p7 | 16:56404872 | CCTGATTCTGAAAGG[C/T]TTGCCCTCTGTTAGA | 267 |
| rs372427781 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56383984 | GCCTATAAGACCCTG[A/C]ATGTTCTGGCTCTGA | 267 |
| rs372454029 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413407 | GTATTCCCAGCTACT[C/T]GGGAGGTTGAAGCAG | 267 |
| rs372457380 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56415963 | TTAAGGTGATGAAAT[A/C]GATGCTAAAAAGACT | 267 |
| rs372464181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368765 | CTATTTATTTTTGTA[A/C]ATAAAGTTTTATTGG | 267 |
| rs372517419 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367836 | CTGAACACCTAACTT[C/T]GGCATGGCACCAAGG | 267 |
| rs372539842 | snp | A/G | 0.000585714 | 0.017103 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362698 | ACAGTTAAAATTTGC[A/G]GTGTTTCTAAGGGGA | 267 |
| rs372760626 | snp | A/T | 0.000161927 | 0.00899651 | intron-variant | AMFR | GRCh38.p7 | 16:56386026 | CAATCCGAGACCCTG[A/T]AACAAACAAGAATCC | 267 |
| rs372893537 | snp | A/C | 0.000131789 | 0.00811648 | intron-variant | AMFR | GRCh38.p7 | 16:56402958 | AAAATGAGTAAACTT[A/C]GGCAACATCAACTTG | 267 |
| rs373039697 | snp | A/G | 0.000263933 | 0.0114846 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362833 | GCTTTTCCATGGAGC[A/G]GGCAGAATTGGGACA | 267 |
| rs373087129 | snp | A/T | 0.00858353 | 0.0649468 | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425363 | GCCCCCAGGCTTCCC[A/T]GCGCTGCGGCCGGGC | 267 |
| rs373167477 | snp | C/T | 0.000142275 | 0.00843311 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362267 | TTTGGACTGGAGGCT[C/T]GGAAAGTCAGTCCCA | 267 |
| rs373191257 | snp | A/T | 3.42771e-05 | 0.00413973 | missense | AMFR | GRCh38.p7 | 16:56363027 | CTCTCTGAGGCCGCA[A/T]CATCTTCAGAACTTT | 267 |
| rs373202881 | snp | C/T | 1.752e-05 | 0.00295968 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364100 | GTCCAGTGGCACACG[C/T]TCGGTCTGGACACGG | 267 |
| rs373247309 | in-del | -/GAG | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56415447 | GAAAGAAAGGGGATA[-/GAG]GAGAGTAATTTAAGA | 267 |
| rs373311427 | in-del | -/ATCC | | | intron-variant | AMFR | GRCh38.p7 | 16:56388033 | TCCATCCATCCATCC[-/ATCC]CACCTAAACACTTTC | 267 |
| rs373344016 | snp | A/G | 1.68097e-05 | 0.00289906 | missense | AMFR | GRCh38.p7 | 16:56364062 | TCGCCGAAGTCCAGC[A/G]TCTCCTCCAGGCGAG | 267 |
| rs373363557 | snp | C/T | 5.43277e-05 | 0.00521161 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408105 | CATCGGCGTGGTGGG[C/T]GAGAAGGAAAGCTGA | 267 |
| rs373608363 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56417503 | AATACAATTGAGCAA[-/C]CCTGATGCAAAAATC | 267 |
| rs373729775 | snp | A/C/G/T | 0.000216159 | 0.0103943 | intron-variant | AMFR | GRCh38.p7 | 16:56401858 | CCTGTGGAAACAAAA[A/C/G/T]AAGCCCAGCAGGAAC | 267 |
| rs373736245 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | AMFR | GRCh38.p7 | 16:56403133 | ACTTAGAGAGAAAGA[A/G]AATAAAACACACGGT | 267 |
| rs373878634 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56363722 | CTGACAGTACCAGCA[C/T]CAGAGGTAGACCAGT | 267 |
| rs373922610 | snp | C/T | 0.000139938 | 0.00836359 | intron-variant | AMFR | GRCh38.p7 | 16:56389401 | GTCCAAAAGAAGATA[C/T]GTCAGCATCCTTGAT | 267 |
| rs373986823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418902 | ATTTCTTAGTCTCCT[A/G]CTTAACAACAGTACT | 267 |
| rs373997548 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386933 | GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT | 267 |
| rs374105085 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391648 | AGTGTGTGATTGAAC[C/T]GCAAGGTGGCAGCGA | 267 |
| rs374154899 | snp | A/C/T | 0.000190858 | 0.00976691 | intron-variant, missense | AMFR | GRCh38.p7 | 16:56388785 | CATCAGTATCACTGT[A/C/T]GACCACCTCCACCTC | 267 |
| rs374209895 | snp | A/C | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426439 | TATACAGACACAGAA[A/C]GTTGATTAATGATTG | 267 |
| rs374297782 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406264 | GCTGGTCTTGAAGGG[G/T]ATTTTTTTTATTACA | 267 |
| rs374417846 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56417794 | AAATCCAGGAAAAAA[-/A]TCCCAAATCCAAAAC | 267 |
| rs374424982 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56393064 | GGGCCAATATTCAAC[A/G]TTCTTAAAGAAAAGA | 267 |
| rs374450228 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56396342 | AAACAGAGATATAGA[C/T]CAATGGAACAGAACA | 267 |
| rs374546862 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56376683 | GTTTCCATCTTAGGA[A/G]ATTAGAAATAGAAGA | 267 |
| rs374598719 | in-del | -/CACG | | | intron-variant | AMFR | GRCh38.p7 | 16:56365599 | AGGTACATACACACA[-/CACG]CACACACACGCTGGA | 267 |
| rs374620631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56410624 | TGGTGGCTCATGCAC[A/G]AAATCCCAGCATTTT | 267 |
| rs374660334 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395288 | ATCCTCAATAAAATA[C/T]TGGCAAACCAAATGC | 267 |
| rs374742792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56381768 | TCATGTGGATACGTG[C/T]CACTATATATTTGTC | 267 |
| rs374813706 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | AMFR | GRCh38.p7 | 16:56406884 | ATATTAGTTGAAAGT[C/T]AGAGAATCAAAAAAA | 267 |
| rs374935530 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424552 | CCTCTTCGTCGGAAG[A/G]AAATCCGCTAACAAT | 267 |
| rs374941038 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56402782 | GTTCTGTTTTCATCC[A/C]TAATTTAGAGGTGAA | 267 |
| rs375013030 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMFR | GRCh38.p7 | 16:56413343 | CCCGGCCAACGTGGC[A/G]AAATCCTGTCTCTAC | 267 |
| rs375019999 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406346 | GAGGTCGAGGCAGGC[C/T]GACTGCTTGATCTCA | 267 |
| rs375064881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391938 | GGGTCCCTGACCCCC[A/G]AGTAGCCTAACTGCG | 267 |
| rs375095676 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56402208 | GGGCGTGGTGACAGG[C/T]GCCTGCAATCCCAGC | 267 |
| rs375125496 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383315 | CTGCCACCTTCTCCT[A/G]GTCTCTTCCCTCTCC | 267 |
| rs375195093 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56417311 | GCTACTGAGGAGGCT[A/G]AGGTGGGAGGATCTC | 267 |
| rs375230622 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56373977 | GTTCAAGACCAGCCT[A/G]GGCAACATGGTGAAA | 267 |
| rs375235439 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387626 | ACTGTTGAAAATCAA[C/T]AGCAGCTTAATGTGA | 267 |
| rs375285843 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56396599 | AAGAAAACCTAGGCA[A/T]TACCATTCAGGACAT | 267 |
| rs375363751 | snp | C/G | 6.74445e-05 | 0.0058067 | intron-variant | AMFR | GRCh38.p7 | 16:56404866 | ACTGTTCCTGATTCT[C/G]AAAGGCTTGCCCTCT | 267 |
| rs375378689 | snp | A/C | 8.28947e-05 | 0.00643743 | intron-variant | AMFR | GRCh38.p7 | 16:56405182 | GTAGGCCTCCATCAC[A/C]TCCCTCCCCAATTTC | 267 |
| rs375492835 | snp | A/G | 0.000153988 | 0.00877328 | missense | AMFR | GRCh38.p7 | 16:56401835 | TCCTCTGGAGTTGCA[A/G]CTGCAAACCTGTGGA | 267 |
| rs375555745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56373242 | TGAAATCAGCCAGGG[C/T]ACACTGTTCTTAACA | 267 |
| rs375642914 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56401127 | CCTCAAGGTCCATCA[A/C]CATCAAAACACCAAA | 267 |
| rs375830973 | snp | C/T | 0.000200733 | 0.0100163 | intron-variant | AMFR | GRCh38.p7 | 16:56369162 | TGTGAAGATAGAACC[C/T]ATTTATCATGCTTTA | 267 |
| rs375878637 | snp | C/G | 1.77587e-05 | 0.00297977 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362371 | ATCGAACCAAGAGTT[C/G]CTTTTCCAAGATGCC | 267 |
| rs375917273 | snp | A/G | 1.66418e-05 | 0.00288455 | synonymous-codon | AMFR | GRCh38.p7 | 16:56409553 | GATGAAAATGAACTT[A/G]TAGAAAATAAAATTC | 267 |
| rs375940825 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56394606 | AAATTAGCCGGGCGC[A/G]GTGGCGGGCGCCTGT | 267 |
| rs375951425 | snp | A/C/T | 4.97181e-05 | 0.00498568 | intron-variant | AMFR | GRCh38.p7 | 16:56401687 | AAAGCACACACACGC[A/C/T]CTGGACAGAACACCT | 267 |
| rs375956428 | snp | C/T | 7.22022e-05 | 0.00600798 | intron-variant | AMFR | GRCh38.p7 | 16:56364113 | CGCTCGGTCTGGACA[C/T]GGGGCAGGAAGCAAG | 267 |
| rs375982293 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56382241 | GTGGATGAACCATGA[C/T]GACATTATGCTAAGT | 267 |
| rs376093691 | in-del | -/GAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56382456 | GCCACACTGGAAGAA[-/GAA]TTGTCTTGAGCCACA | 267 |
| rs376126542 | snp | C/T | 3.29506e-05 | 0.00405884 | missense | AMFR | GRCh38.p7 | 16:56389305 | TGACACGATTATTGT[C/T]GGCAATATTAAGAGA | 267 |
| rs376135211 | snp | A/T | 1.72362e-05 | 0.00293561 | synonymous-codon | AMFR | GRCh38.p7 | 16:56385985 | GGTGTGCATCACTTC[A/T]ACCGAAAAACTCGGC | 267 |
| rs376136617 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390398 | ATCTACGAACATGTG[A/T]AGATATAAAGTTATA | 267 |
| rs376201737 | snp | A/C | 8.32134e-05 | 0.00644979 | intron-variant | AMFR | GRCh38.p7 | 16:56369358 | TACAGAGTCCACAGA[A/C]ACGTTCACTGTTAAC | 267 |
| rs376283954 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant | AMFR | GRCh38.p7 | 16:56363095 | CTCTCTCATAGGAGA[A/G]ATGGGGAGCTGTGGA | 267 |
| rs376364605 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56382005 | AATTAGTCTTAAAAA[C/T]AAACAAAAAAGACTC | 267 |
| rs376401272 | snp | G/T | 1.67175e-05 | 0.0028911 | intron-variant | AMFR | GRCh38.p7 | 16:56363914 | GTGGTCTGGAGAAGC[G/T]ACTCACTTGCGAGCT | 267 |
| rs376417670 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395613 | CATTCCCTTTGAAAA[C/T]GGGCACAAGACAGGG | 267 |
| rs376535705 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56376756 | AATGAGAGCAGACAT[C/T]AATGAAACTGAAAAT | 267 |
| rs376560925 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56381115 | CTCATAATCATGGTG[C/G]AAGGCAAGGAGGAGC | 267 |
| rs376778065 | snp | C/T | 7.71873e-05 | 0.0062119 | intron-variant | AMFR | GRCh38.p7 | 16:56409609 | AAAGAAAAATGTTTA[C/T]GAAGGTGAGTACCAT | 267 |
| rs376876964 | snp | C/T | 1.65277e-05 | 0.00287464 | missense | AMFR | GRCh38.p7 | 16:56408008 | TTCCGTGGGTGTAGC[C/T]GGTGATGGAGCAGAC | 267 |
| rs376898917 | snp | C/T | 0.000137663 | 0.00829533 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362907 | AGGAAGGCAAGGGAG[C/T]GCTAGGAGGTCTGCT | 267 |
| rs376934765 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56399113 | ATTCACCATAATAAG[A/G]AAACACTTCACACCC | 267 |
| rs376972771 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370664 | TGTACTCTGGAGACA[C/T]CTCAGAGTTTATGTA | 267 |
| rs377013496 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56417638 | GCAGACTTACAACAG[-/T]TTACTCAGTGTCCCT | 267 |
| rs377092104 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426238 | ACAACGCTAATGTCC[A/G]TCAAGCGATGAGTGG | 267 |
| rs377180570 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363345 | TGCCAGGGCCCAAAC[C/G]CACTTGAGGAACACA | 267 |
| rs377188397 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56396827 | ACAAAGAACTCAAAC[A/T]AATTTACAAGAAAAA | 267 |
| rs377193130 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56392720 | GGGACTATATGGAAA[A/G]ACCAAATCTATGTCT | 267 |
| rs377202918 | snp | A/G | 0.000135117 | 0.00821828 | intron-variant | AMFR | GRCh38.p7 | 16:56386043 | ACAAACAAGAATCCA[A/G]TGTAAGTTTCAGAGC | 267 |
| rs377241420 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378976 | TAACAGGAACTCTCA[C/T]TCACTGCTGGTGAGA | 267 |
| rs377266208 | snp | C/T | 0.00040833 | 0.0142828 | intron-variant | AMFR | GRCh38.p7 | 16:56409383 | TTCAAAGTTGGCAAA[C/T]GTGGTGACTAAGCAA | 267 |
| rs377286954 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412914 | GGAGACCTCTAGAGT[C/T]GATACTGGAGAAAGT | 267 |
| rs377298050 | snp | C/T | 3.50201e-05 | 0.00418436 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362866 | CCTCCTCCAGTCAGT[C/T]GGGCACAGGGCGCAG | 267 |
| rs377373737 | snp | G/T | 5.02273e-05 | 0.0050111 | intron-variant | AMFR | GRCh38.p7 | 16:56369157 | ATCTTTGTGAAGATA[G/T]AACCCATTTATCATG | 267 |
| rs377449109 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375165 | CTTTCTTAAAACGTT[A/G]TATTTTTAATTTTCT | 267 |
| rs377518120 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371479 | GGTGGGGTGGTCCAG[C/G/T]TGCAGAGCTTCAACA | 267 |
| rs377540043 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56403592 | TATAACTATCTTTAT[C/G]AAACTAATACATGAT | 267 |
| rs377583003 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399300 | GATCCAGAAATTCCA[C/T]TCCTAGGCATATACC | 267 |
| rs377590825 | snp | A/C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387484 | CAACACGACACCATC[A/C/T]CCACTGTACTCCATT | 267 |
| rs377678972 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56376006 | GAGGTTGCAGTGAGC[C/T]GAGATCGGGCCACTG | 267 |
| rs377680116 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56391883 | CGTTCTCCCAGCATG[A/G]AGTTTGAGATCTGAG | 267 |
| rs377723444 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | AMFR | GRCh38.p7 | 16:56408126 | GGAAAGCTGAAATGC[A/G]CACAGTAGGAAACTG | 267 |
| rs377724509 | snp | C/G | 0.000100791 | 0.00709827 | synonymous-codon | AMFR | GRCh38.p7 | 16:56363002 | GGACGCACCTTCCGA[C/G]GGGAGGAAGCTCTCT | 267 |
| rs386384779 | in-del | -/CA | | | intron-variant | AMFR | GRCh38.p7 | 16:56365553 | CATGTACACACACAC[-/CA]ACACAGACACACGTA | 267 |
| rs386384780 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56387110 | AAAAAAAAAAAAAAA[-/AA]ATCAAGTGGAATGGC | 267 |
| rs397811798 | in-del | -/CA | | | intron-variant | AMFR | GRCh38.p7 | 16:56365558 | ACACACACACACACA[-/CA]GACACACGTAGTTGG | 267 |
| rs397960827 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56404052 | TTTTTTTTTTTTTTT[-/T]GGGACGGAGTGTCAC | 267 |
| rs398078660 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56399092 | ATTACTAAAAAAAAA[-/A]ACAAAATTCACCATA | 267 |
| rs527296807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414136 | GAATCTGGATAAAGG[G/T]TATATAGGAGTTTTC | 267 |
| rs527298921 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56422859 | TTTTAAATTGTGTTT[G/T]TTCATGAAAAACCTC | 267 |
| rs527336585 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372671 | CCTATGCACATACCA[C/G]ATGTGCTTTCGAATC | 267 |
| rs527420889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56417762 | AAATATTTCATTATG[C/T]ATATGCAAATATTCC | 267 |
| rs527439063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56407260 | AGCCAATTAGCTTCA[A/G]TTTATCTAATATCTC | 267 |
| rs527444415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393652 | TCAATTCAACAAGAA[A/G]AGCTAACTATCCTAA | 267 |
| rs527451211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401277 | TCTGTGCTGTTTAGC[A/G]GTCCTGGTCTAGTCC | 267 |
| rs527471743 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379279 | AGCTTGTGCAGGTGA[A/T]CTCCTCTTTTTAAAA | 267 |
| rs527579213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56394395 | AGAGACACAAAAAAC[C/T]CTTCAAAAAAATCAG | 267 |
| rs527637220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56398345 | AAATGTATCATATAT[A/G]TAATATATCATTATA | 267 |
| rs527773258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392314 | CAGAGTGCCTCTCCT[C/G]CTCCAAAGGAATGCA | 267 |
| rs527803828 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56376250 | AAGAACATAGCTGAA[A/C]TCAATAACACCATCA | 267 |
| rs527924015 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56413938 | ATTTTTTCAATGTTA[A/G]ATTTCCTAATTTTAA | 267 |
| rs528045187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383922 | GGGGTCTGTAAGAAG[C/T]TCTGAATGGCCTTCT | 267 |
| rs528069911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377692 | TCTGCAGATGACATG[C/G]TCACCTATGTAGAAA | 267 |
| rs528106731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56391402 | AGCAGGGCAAGGCAT[C/T]GCCTCACCCGGGAAG | 267 |
| rs528163637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418955 | CCATTTCTGGAAGAG[A/T]GAAGCAGGTAACAGG | 267 |
| rs528281749 | in-del | -/C | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425845 | GCCGTCGGCCACTTG[-/C]CCCCCCCCCACCCCA | 267 |
| rs528305173 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56419600 | CAGTTCAAGACCAGC[A/C]TGGCCAACATGGTGA | 267 |
| rs528316315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364675 | CCACAGCCTCAACCT[A/C]CCCAGGCTCAGGGGA | 267 |
| rs528326204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370284 | TAAAATTCAAATACA[C/T]CATGTTAGGTGAAAG | 267 |
| rs528356732 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56405104 | ATTTGGTTTAACCAT[C/G]TTGTAATTTAGTCCG | 267 |
| rs528470685 | snp | C/T | 3.57341e-05 | 0.00422679 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362455 | ATGCTTCCACAACAA[C/T]GACAGCAGTTTGATA | 267 |
| rs528519826 | snp | C/T | 3.52373e-05 | 0.00419731 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362832 | CGCTTTTCCATGGAG[C/T]GGGCAGAATTGGGAC | 267 |
| rs528535350 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402726 | ACCATTCTAAGTACA[C/T]GAATTATCTCACCAA | 267 |
| rs528625255 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56418291 | AGGGAGAATCACGAC[A/G]TCAGGAGTTCAAGAC | 267 |
| rs528656368 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56396997 | TATCATCTCACACCA[C/G]TTAGAATGGCGATCA | 267 |
| rs528779236 | in-del | -/AA/AAA | 0.499997 | 0.00119808 | intron-variant | AMFR | GRCh38.p7 | 16:56387095 | GCAAGACTCCATCTC[-/AA/AAA]AAAAAAAAAAAAAAA | 267 |
| rs528868073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385356 | ACGCAGTGGCTCACG[C/T]CTGTAATCCAAGCAC | 267 |
| rs528873002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370953 | AAGGAGCAGGGAGTA[C/T]GTCAACGTCAGGACC | 267 |
| rs528924565 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422787 | TTACTGAGGGTAGGG[A/G]AAAGTGTTGTTCACA | 267 |
| rs528963683 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56420894 | TTGCATAATTAAGTC[A/C]GAACCTTGACAGTAG | 267 |
| rs528976729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412583 | GAAGCATTTAAGCCA[A/G]TAGAAGTGGCTCACA | 267 |
| rs529006837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56378024 | TCCATTCTTCCCAAC[C/T]TGATGTACAGATTCA | 267 |
| rs529258062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418763 | CAGTGAACCGAGATC[A/G]CGCCACTGCACTCCA | 267 |
| rs529258181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411020 | AGCAGTCCTGTAAGT[A/G]TACATTCCCATGGGC | 267 |
| rs529320270 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56382715 | AATGTGAATACACCA[C/T]TGAAATGCACATCTG | 267 |
| rs529377634 | snp | C/T | | | missense | AMFR | GRCh38.p7 | 16:56403112 | ATAACCAGATGTTGC[C/T]AAATAACTTAGAGAG | 267 |
| rs529394282 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56411532 | ATGTAATTTGGAACC[A/G]TGTAAATGTTTCACA | 267 |
| rs529471928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391412 | GGCATCGCCTCACCC[A/G]GGAAGCGCAAGGGGT | 267 |
| rs529576780 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426485 | AAGAGGGGAGTAGGG[A/G]GTGATAAAGGGTGCA | 267 |
| rs529605386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396064 | AAGAACATTCCATGG[C/T]CATGGATAGGAAGAA | 267 |
| rs529610313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56384032 | CAGTGTTGTTCCCCT[A/G]CTTGCCAGGCCCCAA | 267 |
| rs529612161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391619 | CACGGAGCCTCGCTC[A/G]TTGCTAGCACAGCAG | 267 |
| rs529628413 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56364262 | GGAACCACAAGCTAC[A/G]GATAATGGAGCAGCA | 267 |
| rs529665341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395431 | CAAAGACAAAAACCA[C/G]ATGATTATCTCAATA | 267 |
| rs529699276 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394719 | CTGCAGTCCGCAGTC[C/T]GGCCTGGGCGACAGA | 267 |
| rs529729242 | snp | C/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361889 | ATTTGGGACCTGGGC[C/T]CTCTCCAAGGCAGGT | 267 |
| rs529737710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390026 | CTCAATGTCCTCCAC[C/T]CTCTTCTCTTTGCAC | 267 |
| rs529777951 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56392372 | GGACAGAGAATGACT[C/T]TGACAAGTTGAGAGA | 267 |
| rs529822352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382701 | GGTGATAGTTGCACA[A/G]TGTGAATACACCACT | 267 |
| rs529934756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382153 | ATTAATAGATAAATA[A/G]AATGTGGTATATGCA | 267 |
| rs529958700 | snp | A/G | 0.000119164 | 0.00771802 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408081 | GGACAGGACTCGACC[A/G]TGGCTGCTCATCGGC | 267 |
| rs530002895 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402657 | TCTATTTGATAATAA[C/T]GACAATAAAATCATG | 267 |
| rs530030236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375974 | GAGGGAGGAGAATCG[C/T]TTGAACCCAGGAGGT | 267 |
| rs530076288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380648 | TTCTTCTACCAGATA[C/T]TCTAAATCATATGTC | 267 |
| rs530097046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374091 | GAAGAACTGCTTGAA[C/G]TCAGGAGGTGGAGGT | 267 |
| rs530149374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56387730 | TCCTTTTAACACTGC[C/T]GGGAGGCAGAACATT | 267 |
| rs530187455 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424460 | GAGACGGCCTCTCTC[C/T]AACCGGAATGTCCAA | 267 |
| rs530189289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56416184 | CATTTAGCACTTGTT[C/T]GAGGCATGTGGGAAA | 267 |
| rs530212938 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361633 | TATCACCTTTTTCAA[C/T]TACTTTTCAACATTC | 267 |
| rs530271274 | snp | A/G | 1.77357e-05 | 0.00297784 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362322 | ACTTCATCACACCCT[A/G]TAGCCCTGGACTTTC | 267 |
| rs530283767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367049 | GCATCTCAATGGCCT[C/T]GGCTCCCTGGAGAGC | 267 |
| rs530284961 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56374854 | TTTAACATAACATTC[A/G]ATTCAAAATAACAGC | 267 |
| rs530327528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417181 | TTCGGAGGCCAAGGT[G/T]GGGGGATTGCTTGAA | 267 |
| rs530343295 | snp | A/G | 1.64925e-05 | 0.00287158 | intron-variant | AMFR | GRCh38.p7 | 16:56367536 | CTGACCGCTGGAAGA[A/G]AAACAGTACCAAAAA | 267 |
| rs530390903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390680 | TCCAATTCTCCTACT[A/G]ACACCTTTAAATCAC | 267 |
| rs530470209 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56409363 | GGCTCATTCACATTA[C/T]ACAATTCAAAGTTGG | 267 |
| rs530522179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56382990 | TTGTAAATAAATGAC[C/G]TATTCAAAAACCTTA | 267 |
| rs530527145 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385754 | TCAAAATTTAAAACA[C/T]AGGAATGTAAATGGT | 267 |
| rs530556420 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56410006 | AACCCCATCTCTACC[-/A]AAAAAAAAAATACAA | 267 |
| rs530589898 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426627 | GCTGGGATTACAGGC[A/G]TATGCCACCACACCT | 267 |
| rs530591890 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56366859 | GCACCTCGGCCCTGC[A/T]GCTTGGAGTTAGGGT | 267 |
| rs530632706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391369 | GACAGTGGGTGCAGC[A/G]CACCGAGCATGAGCC | 267 |
| rs530640820 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56395254 | TAGACCAATATCCCT[C/G]ATGAACATCGATGCA | 267 |
| rs530676711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56376902 | TACTAATACAAGAAA[C/T]ATTATACAGATAACT | 267 |
| rs530692283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411721 | TCCATCAAAAGGGCA[A/G]AGACACCCTAGTGGT | 267 |
| rs530781473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370679 | TCTCAGAGTTTATGT[A/G]GGGCTCTAGGGTGGG | 267 |
| rs530902406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381960 | GTACCTTCTTCTTAA[C/T]TTTGCTGTAAGCCTA | 267 |
| rs530920430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367626 | GAGCTATGGTACCCA[A/G]TCCAACCTGTAACTC | 267 |
| rs530936434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424572 | CCGCTAACAATCCCA[C/T]GCCTGACCAAGTGGG | 267 |
| rs530946954 | snp | C/T | 0.0142736 | 0.0832652 | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425399 | CGGCGGCCTCGCGAA[C/T]GGCGCCCACGGGCTC | 267 |
| rs530966186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381415 | TAAATGTTTATAGCA[C/G]CTTTATTCATAACTG | 267 |
| rs530986602 | snp | C/T | 1.77631e-05 | 0.00298014 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362728 | AAGAGAAATGTCACA[C/T]AGAAAGTATTACAAA | 267 |
| rs531063240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368397 | CCACATCTAATATCT[A/C]AGCCCATGTGACTGA | 267 |
| rs531085620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377698 | GATGACATGCTCACC[A/T]ATGTAGAAAATCTGG | 267 |
| rs531223522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396106 | AAAATGGCCATACTG[C/T]CCAAGGTAATTTATA | 267 |
| rs531223954 | snp | A/G | 0.00109021 | 0.023322 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408009 | TCCGTGGGTGTAGCC[A/G]GTGATGGAGCAGACG | 267 |
| rs531248128 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373293 | CTACTCAACCAGAAC[C/T]TCATCTGCTGGGGTC | 267 |
| rs531370832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395231 | GACACAACAAAAAAA[C/G]AGAATTTTAGACCAA | 267 |
| rs531386988 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56366244 | TTAGCCAGGCGTGGT[A/G]GTGGGCGCCTGTAGT | 267 |
| rs531416449 | snp | C/T | 7.01262e-05 | 0.005921 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362842 | TGGAGCGGGCAGAAT[C/T]GGGACAGGCCTCCTC | 267 |
| rs531517957 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386775 | GGCTGCTTTTCATTC[C/T]TTCACAAAGAAACAC | 267 |
| rs531593316 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | AMFR | GRCh38.p7 | 16:56421908 | TTGTTAGTGTAAAAA[C/T]CCTGAAGTCTCCTCC | 267 |
| rs531605163 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56389520 | TGAGATTTAAGTGTT[A/G]AGAAGCATTTATGGA | 267 |
| rs531695466 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56392904 | AGCAACTCCAAGACA[C/T]ATAATTGTCAGATTC | 267 |
| rs531823564 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386834 | GCCAGGAGCAGTGGC[A/T]CACGCCTGTAATCCA | 267 |
| rs531832543 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56421181 | TGGGCAGCTCCTGGC[C/G]TCAAGCAATCCTCCA | 267 |
| rs531859312 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56392733 | AAGACCAAATCTATG[C/T]CTGATTGGTGTACCT | 267 |
| rs531864757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414964 | GCTTGGTGTTGGCTT[C/T]GAAGTAAAGGTTTTG | 267 |
| rs531868661 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56418681 | GGGCACATGGTGGGC[A/G]CCTGTAGTCCCAGCT | 267 |
| rs531889278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423708 | GATTTGAAATTAAGC[A/T]AGAGATGTGAGTTGA | 267 |
| rs531999736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418666 | TACAAAAAATTATCC[A/G]GGCACATGGTGGGCG | 267 |
| rs532001086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401479 | AATGGAGAAGAAATA[C/T]GAAGACAGCTACCAT | 267 |
| rs532070838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395327 | ATCAAAAACCTTATC[C/T]GCCATGATCAAGCTG | 267 |
| rs532072611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423100 | AAAGGCACCACCACA[C/T]AGGGTATTCACTCAA | 267 |
| rs532091468 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402096 | TAATCCCAGCACTTT[C/T]GGAGGCCGAGGTAGG | 267 |
| rs532176288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56389949 | TCAAGCATGACAGCC[A/G]TACAGGTCCTTACCT | 267 |
| rs532183813 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56389797 | TCACTCTGCTTTAGC[C/T]ACCACCAGCACAGTC | 267 |
| rs532221553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56413592 | TATACAGTATGCTTG[C/T]GGCGTAATTCTTCAT | 267 |
| rs532247232 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425635 | CCCCAGCGGTCGCGC[A/C]GCCGCCTAGCGGGCG | 267 |
| rs532301699 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381512 | AGACAATGGAATATT[A/T]TTTGGTGCTAACAAG | 267 |
| rs532310534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382096 | CAGTAGCATTATTCA[C/T]GATAGCTAAAATGTG | 267 |
| rs532367183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | AMFR | GRCh38.p7 | 16:56388816 | CTGTCCCACTGGAAC[A/G]TCTTCAGGGGCAGTA | 267 |
| rs532410369 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363672 | ACACAAGTGCTCTCT[C/T]GGCAAGCGTGGCCAA | 267 |
| rs532473911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380027 | GCATTCTGCGTAGGG[C/G]CTCTGATCCCACATT | 267 |
| rs532504157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386946 | TACTAAAAATACAAA[A/G]ATTAGCCAGGCATGG | 267 |
| rs532569850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393562 | GAGATTGCAATCCTA[A/G]TCTCTGACAAAACAG | 267 |
| rs532609467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380479 | TATGCAAATTTCTGC[A/G]GCCAGCTTGAATTTC | 267 |
| rs532723464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367005 | TGTATCTGGAAATCC[C/T]GAGTTTGACAAGTGA | 267 |
| rs532777674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364871 | GACTACAGGCATGAG[C/G]CACTGTGCCCAGCCC | 267 |
| rs532786546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56415035 | AGAAAACCGGCGAGA[A/G]GGGCCAAGAGATGAA | 267 |
| rs532817984 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368577 | ATATTAATACTTCTT[A/G]TGCTCATCAAAGTAG | 267 |
| rs532888639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415915 | AATTTTTTAAAAAGA[A/G]AAAACAATTCAGGTA | 267 |
| rs532943655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372530 | AACCAAATTTCAATA[C/T]GCCCGTAGCTATATC | 267 |
| rs533041723 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418490 | GCCTAGGTGACAGAG[-/T]GAGACTCCATCTCAA | 267 |
| rs533068396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393073 | TTCAACATTCTTAAA[A/G]AAAAGAATTTTCAAG | 267 |
| rs533083200 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56371917 | ACCATTTACTCAGCA[A/T]TTACATTGTATTAGG | 267 |
| rs533111682 | snp | A/G | 0.000280549 | 0.0118404 | synonymous-codon | AMFR | GRCh38.p7 | 16:56405011 | TTCCCACGTCCCTTC[A/G]TGGTTGAGGTCCCAG | 267 |
| rs533112231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407783 | AAGAGTTACATAAAA[C/T]ACCACACAAAAGCAT | 267 |
| rs533114561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56399420 | CAACCCAAATGTCCA[C/T]CAATGGATGAATGGA | 267 |
| rs533227435 | snp | A/C | | | synonymous-codon, missense | AMFR | GRCh38.p7 | 16:56386021 | GCTCGCAATCCGAGA[A/C]CCTGAAACAAACAAG | 267 |
| rs533257470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400126 | CTCTACTTCTACCAC[C/T]AGAGTCCAAGCTACT | 267 |
| rs533278198 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383334 | TCTTCCCTCTCCACC[A/G]GCTGTCATGGCTCCT | 267 |
| rs533374758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412351 | GCTGGATAAGAAATA[C/T]GCTCATTATAATTAC | 267 |
| rs533478096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363850 | TTAAAAAGAGAAGAC[A/G]GCCTGACAACGGCCT | 267 |
| rs533643092 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56401077 | AACTTTCCCAATATG[C/T]AAAATTGAAAACACA | 267 |
| rs533680620 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56385387 | TTTGGGAGGCCAAGG[C/T]GGATGGATCACTAAG | 267 |
| rs533737780 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403910 | TAAATACAAAAAATA[C/T]ATAAAAAGAAGCAGT | 267 |
| rs533853059 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56381464 | CAAGATGTCCTTAAG[C/T]AGGTGAACGAATTAA | 267 |
| rs533860458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392562 | ACGAGAACTACGTGA[C/T]GAATGCACAAGCTTC | 267 |
| rs533891625 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56391746 | ACTGAGTGGAGCCCA[C/G]CGCACCTCAAGGAGG | 267 |
| rs533900330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384128 | CGGCCTCCTTCCCCC[C/T]GATCCAGCTCCATCT | 267 |
| rs533924315 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56398609 | GTAAATATACAGATA[C/T]TAAAAAAAAAAATCA | 267 |
| rs533948709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386417 | TGCAGCCCAGCCCAG[A/C]GCCCTCACACGCTCA | 267 |
| rs534001220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56393187 | TTTGTCACCACCAGG[C/T]CTGCCCTAAGAGCTC | 267 |
| rs534091497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379769 | CTCCAAAATGATCTC[C/T]GCTGAATCCATGTCT | 267 |
| rs534233143 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56364737 | ACCACAGGCTCGTGC[C/G]ACCACATCTGGCTAA | 267 |
| rs534258293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56412817 | TGAGTGGAGATCGCA[C/T]CACTGCACTCCAGCC | 267 |
| rs534381784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56376035 | TGCACTCCAGCTTGC[C/G]CAACCAAGTGAGGCT | 267 |
| rs534384195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372019 | TCCCCCATCTTTTTT[C/T]TTTACCTTAAACTAT | 267 |
| rs534386196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364399 | ATGAAAAACGTAAGC[A/C]CCTTCAAGCTGCACT | 267 |
| rs534554999 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386376 | CCCTTCACTGCTGAG[C/T]AATCCTGCTTTCCAG | 267 |
| rs534568289 | snp | C/T | 2.39146e-05 | 0.00345785 | intron-variant | AMFR | GRCh38.p7 | 16:56363084 | GAAGACTTTTTCTCT[C/T]TCATAGGAGAGATGG | 267 |
| rs534595188 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418006 | CATCTCTACTAAAAA[C/T]ACAACAAATGTAGCC | 267 |
| rs534597871 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426738 | CTCCCACCTTGCCTT[C/T]ACAAAGTGCAGGGAT | 267 |
| rs534605842 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425765 | CCGCGGCGCAGGGGT[C/T]ACTCGGGCTCGCAGG | 267 |
| rs534645685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383060 | AGCTACCACCTCTAC[C/T]GCTCTGTGTCCTTCT | 267 |
| rs534649029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56397193 | TATATACCCAAAGGA[A/G]TATAAATCATGCTGC | 267 |
| rs534720188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409896 | AAATAGGCCAGGCGC[A/T]GTGGCTCATATCTGT | 267 |
| rs534740733 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56418468 | GAGATCATGCCACTG[C/T]ACTCCAGCCTAGGTG | 267 |
| rs534828215 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361905 | CTCTCCAAGGCAGGT[A/G]GGTTCACACCTTACC | 267 |
| rs534948049 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56422747 | CATTTTATTTATCTA[C/T]TATCCCCTATAAAAT | 267 |
| rs534968187 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56404548 | GTAGCTAACACTGCA[C/G]GAATTCCCATTACCA | 267 |
| rs535076493 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361164 | CAACGTGTGAAGTAT[A/G]ATGTAATTCGAGGAC | 267 |
| rs535077235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56367837 | TGAACACCTAACTTC[A/G]GCATGGCACCAAGGA | 267 |
| rs535103984 | snp | A/G | 0.00011533 | 0.00759287 | synonymous-codon | AMFR | GRCh38.p7 | 16:56403050 | TCGACGTTGCACCTC[A/G]TGAAACAGGTAACGC | 267 |
| rs535241900 | snp | A/G | 6.99606e-05 | 0.005914 | intron-variant | AMFR | GRCh38.p7 | 16:56389402 | TCCAAAAGAAGATAC[A/G]TCAGCATCCTTGATT | 267 |
| rs535251502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396128 | TAATTTATAGACTCA[A/G]TGCCATCCCCATCAA | 267 |
| rs535294936 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425854 | CACTTGCCCCCCCCC[A/C]ACCCCATTAACCCTC | 267 |
| rs535336512 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374904 | TGTGCTTGTGCACGT[C/G]TGTGCTTATGTACTC | 267 |
| rs535351112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56391869 | TTGAAGAGAGTAGTC[A/G]TTCTCCCAGCATGGA | 267 |
| rs535389112 | snp | A/C | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425855 | ACTTGCCCCCCCCCC[A/C]CCCCATTAACCCTCT | 267 |
| rs535587224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411990 | ACAATAGGTCTTATA[A/G]TAACAGCATATACCT | 267 |
| rs535590110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398172 | TATAACTCTATCATT[A/T]ATATATATAACTCTA | 267 |
| rs535805513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56389030 | TTATGGGACCACTGC[C/T]ATATATATGGTTTGC | 267 |
| rs535850398 | snp | C/T | 0.000648885 | 0.0180006 | intron-variant | AMFR | GRCh38.p7 | 16:56403145 | AGAGAATAAAACACA[C/T]GGTAAAAGCGAACGT | 267 |
| rs535869312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388067 | TAAAATTGAAATACA[A/G]TCAATGCGTAGCTTA | 267 |
| rs535934452 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424969 | CAGGCGCTCGCCCTC[C/G]GGGGTCCCTGGCGGA | 267 |
| rs535963757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381613 | TAAAAAGGCTACATA[C/T]TGCAGGATTCCACCT | 267 |
| rs536040718 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56417398 | AGCCTGAGCAACATA[C/G]TGAGGCCTTGTCTCA | 267 |
| rs536122508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375316 | ACAAGTATACTGATA[C/T]GCTAAGAAAGGAGAA | 267 |
| rs536123459 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56418512 | CCATCTCAAAAAAAA[A/C]CAAAAAACAAAAAAA | 267 |
| rs536187687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417954 | AGTTGCTTGAGTCCA[A/G]GGGTTCGAGACCAGA | 267 |
| rs536206588 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56381090 | TACAGTTCCACATGG[C/G]TGGGGAGGCCTCATA | 267 |
| rs536237428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366477 | CCAATTACATAGGTG[A/G]ATATGAAAATCTTAA | 267 |
| rs536284251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380063 | TCCGCACTGCCGTAG[C/T]AGAGGTTCTCCATGA | 267 |
| rs536287528 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56365355 | ACTGTGTGTGTCCTG[A/G]AGCTTGGATAGGGCT | 267 |
| rs536296257 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56395563 | TTATGACAAACCCAC[A/G]GCCAACATCATACTG | 267 |
| rs536321542 | in-del | -/AG | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361453 | ACACAACACACCAAT[-/AG]AGTTTGCTTTTTATT | 267 |
| rs536333240 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56422098 | ACTCCTCCATGCCCC[A/C]CCCCCACTTAAGCCC | 267 |
| rs536360239 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390250 | CAACCTCTATTGACT[A/G]GTCCTCTCCACTAAA | 267 |
| rs536373381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365900 | ATGACCAAAAATGTT[C/G]CACAGCAAGGTTCCC | 267 |
| rs536376057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424156 | GATCAGTCTGAAATT[A/C]TCTGTTCTAATGAAC | 267 |
| rs536439351 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362074 | GTTCAAGGACCAAAC[C/T]CACAGGCTTTAGCAC | 267 |
| rs536454928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408598 | GTGATGTCAGCATTA[C/T]GCAAGGAGAGGCAAC | 267 |
| rs536533557 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56394675 | GTGAACCCGGGAAGC[A/G]GAGCTTGCAGTGAGC | 267 |
| rs536577686 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367973 | CTGGGGACCAGCCAG[A/T]AAGGTCTCGCCACCT | 267 |
| rs536591051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401534 | ATGGGTGGGAAACAG[A/T]CCTATGATGTAGGGA | 267 |
| rs536651748 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414509 | GGCACACTGTTCTGG[G/T]GAGTGGGTGTTAGGG | 267 |
| rs536722364 | snp | A/C | 0.000252312 | 0.0112291 | intron-variant | AMFR | GRCh38.p7 | 16:56408130 | AGCTGAAATGCACAC[A/C]GTAGGAAACTGCTCA | 267 |
| rs536733449 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56393850 | AACTCAGCTCTGCAC[C/G]CAGCAGACCTAATAG | 267 |
| rs536748451 | in-del | -/CTA | | | intron-variant | AMFR | GRCh38.p7 | 16:56364477 | ATTTTCTGTTCACTT[-/CTA]CTAATTGCTCAAACA | 267 |
| rs536772884 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419476 | AGTAACAAACCAAAA[C/G]AAGTTCTCCTGTTAC | 267 |
| rs536784382 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375399 | TGGAAGACAAAAATA[G/T]GAACAAAAAACAAGG | 267 |
| rs536863707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400962 | AAAATCTGTCAACAT[A/G]TGTGTTGAGTTACCG | 267 |
| rs536969604 | snp | A/C | 3.55158e-05 | 0.00421386 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362546 | CCACTGGGTGTGGTG[A/C]TCAGGACACCTGCAT | 267 |
| rs536988418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411070 | TTCACTGTACTCTTT[C/T]ACACAGAGGGCTTCC | 267 |
| rs536990343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403182 | GCTAGTGATGAAGGC[A/G]CAGTATGCAGCGGAA | 267 |
| rs537032370 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56360969 | TGTAAAATGGAAGGG[C/T]GGACTGAGAACTTCA | 267 |
| rs537050292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56416321 | AGAGTAATGATGGAG[A/G]AAAAAAACAAATTTA | 267 |
| rs537088870 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370438 | GCCAGGGGCTGAAGG[C/T]TGGGGAAGGACATGA | 267 |
| rs537304043 | in-del | -/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426963 | CATCCCCAGGGCCTG[-/T]TAAGAGTTCTCAGCC | 267 |
| rs537330397 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419773 | CACTCCAGCCTGGGC[A/G]ACAGAGAAAGACTCT | 267 |
| rs537512515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366669 | GCAGGAAAGCCCCAC[A/G]TGGCACAAACACAGA | 267 |
| rs537517798 | snp | C/T | 3.36717e-05 | 0.00410302 | missense | AMFR | GRCh38.p7 | 16:56409566 | TTGTAGAAAATAAAA[C/T]TCCAAAATTTGTCTT | 267 |
| rs537529942 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397942 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
| rs537532511 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393792 | ACTGTCAACATTAGA[C/G]AGATCAACGAGACAG | 267 |
| rs537539474 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56367886 | CTCGTCTATCTTCAC[A/G]TCCTATGAAACAGGT | 267 |
| rs537659839 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402231 | ATCCCAGCTACTCAG[G/T]AGGCTGAGGCAGGAG | 267 |
| rs537799074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393237 | TGGAAAAGAACAACC[A/G]GTACCAGCCACTGCA | 267 |
| rs537808744 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412790 | CTTGAGCCCAGGAGG[C/T]TGAGACTGCAGTGAG | 267 |
| rs537812511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385445 | ACATGGTGAAACCTC[A/G]TCTCTACAAAAATTA | 267 |
| rs537851066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371459 | TTGACTTTTTAAAGG[A/G]GGTCGGTGGGGTGGT | 267 |
| rs537860231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399644 | GCCAGGTGATGGAGA[A/G]GGAAGGAATGGAGAG | 267 |
| rs537875015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385087 | GATTACAGGCATGAG[C/T]CACCATGCCCAGTCT | 267 |
| rs537879613 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56392424 | CTTCTCCAAGCTAAA[G/T]GAGGAAGTTTGAACC | 267 |
| rs537929153 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56386577 | TTTTTCTTTAATCTT[A/G]AAAGCCGTGGTTTTC | 267 |
| rs537931761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407526 | AGGTGGGACTACAGA[C/T]GTGCGCCACCACGCC | 267 |
| rs537981871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420206 | CCAACAGGTGCTTAT[C/T]TATGACCTTGCAAAG | 267 |
| rs538002434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380200 | CTCGCAGGCTCAACA[C/G]CACCTGAAGGCTGCC | 267 |
| rs538044615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365649 | CTATCCCTCTCCTCT[A/C]AGCCTGACCCTAGAG | 267 |
| rs538109809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415336 | CTCCAATTCAATGTA[A/C]AGCTGCTTCTGCCTC | 267 |
| rs538139220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380749 | CAAGAGTCACCCTTG[C/T]TCCAGTTCCCAACAA | 267 |
| rs538181303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372709 | AAAAAACAACAGCCT[A/G]ACACAGTGGCTCACG | 267 |
| rs538184351 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56383443 | GATGTCACCTCCAGG[A/C/T]GTCAATCTCCCAAAT | 267 |
| rs538185557 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56406710 | ATGAATGTAAGAAAT[G/T]ATTTAGTTTAAAATA | 267 |
| rs538189789 | snp | A/G | 1.65132e-05 | 0.00287339 | synonymous-codon | AMFR | GRCh38.p7 | 16:56414273 | CTCACTCACTCGAAG[A/G]GGGCCAAACACAATA | 267 |
| rs538269229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393863 | ACCCAGCAGACCTAA[C/T]AGACATCTACAGAAC | 267 |
| rs538301364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421281 | AGTTTTATAATAATA[C/T]GAAAATCGGCTCTTT | 267 |
| rs538337849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56379019 | ACAGCCACTCTGGAG[A/G]ATGATTCGGCAGCTT | 267 |
| rs538344307 | in-del | -/AAATAAATAA | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56417421 | TTGTCTCAAATAAAT[-/AAATAAATAA]TATTGTGTCATACAT | 267 |
| rs538349820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387997 | ATGCCTGGAACCCCT[C/G]TGTTTGTTCTATCTC | 267 |
| rs538443016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424054 | GGCTTTAAATCCTGG[A/G]GAAACTTTTCTGATC | 267 |
| rs538470366 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361669 | ACTTTCCGTTATGTA[A/G]AATACATTTAAACTT | 267 |
| rs538488617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380841 | ATTTTGGTTAAAGCC[A/G]TTCAACAAGTCTCTA | 267 |
| rs538561405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56365249 | CATACACTTGAGAAA[C/T]CTACAGAAAGAAACT | 267 |
| rs538566661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390549 | GAGTGTGTGACAGTC[A/G]TGTTCCAAAATAATG | 267 |
| rs538586361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387144 | CTCAAAGGTCTTGAG[A/G]TGGGTACAAACAAAA | 267 |
| rs538601821 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56391132 | AAAGCAAACCAAGAG[C/G]ATATCCTAACAACTA | 267 |
| rs538642089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56372734 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 267 |
| rs538715329 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387141 | TATCTCAAAGGTCTT[A/G]AGATGGGTACAAACA | 267 |
| rs538720941 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56422059 | TGCTCCCAATCTTCT[-/AA]AAGAAATCATGCCAG | 267 |
| rs538731862 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380258 | CCCAATGGCCCCTTT[A/C]AGCCATGGCTGGAGC | 267 |
| rs538737723 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56415896 | CCTACTGAAAAATAT[A/G]TAAAATTTTTTAAAA | 267 |
| rs538753374 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383905 | CCCTGGTGGTGGTGG[G/T]GGGGGTCTGTAAGAA | 267 |
| rs538753520 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56411790 | ATATCATTGCCCAAT[A/G]ACGTGAACTAGGAAT | 267 |
| rs538780891 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56372193 | CGCAACAGATCTGAA[A/C]TTTTTCATCTTGCAA | 267 |
| rs538858624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407445 | GGAGTGCAGTGGCGC[A/G]ATGTCTGCTCACTGC | 267 |
| rs538899980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408837 | CGGGTTTAACTGAGG[C/G]GCAGCACTGTAGATG | 267 |
| rs538929318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400763 | AGCTCTCAAGAACCA[C/T]GTTCCTTTGCTTTAA | 267 |
| rs538962595 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56393426 | GACTGGCAAATTGGA[C/T]AGTCAAGACCCATCA | 267 |
| rs538965850 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56374296 | AAAGAGAAACGAACA[C/G]AAGAAATATTTGAAA | 267 |
| rs538984097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366369 | GGTGACAGAGCGAGA[A/C]TCCGTCTCAAAAAAA | 267 |
| rs539005512 | in-del | -/GAA | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56382450 | CCCTGGGCCACACTG[-/GAA]GAAGAATTGTCTTGA | 267 |
| rs539012285 | snp | A/G | 0.000199544 | 0.00998661 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408054 | GCAGGAAAGCAGCAT[A/G]GCAACCAACAGGGAC | 267 |
| rs539118719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363680 | GCTCTCTCGGCAAGC[A/G]TGGCCAAAGGGGTCC | 267 |
| rs539274060 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56391902 | TTGAGATCTGAGAAT[A/G]GACAGACTGCCTCCT | 267 |
| rs539287558 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419540 | GCTCATGCCTGTAAT[C/G]TCAGCACTTTGGGAG | 267 |
| rs539304028 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56365203 | ACCATTCGTATCCCC[A/G]AGAGTCAAAGGACGG | 267 |
| rs539406956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391039 | GTGCCTGCAGGAATA[C/T]AGACATTACCTTTAT | 267 |
| rs539478012 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56371059 | CCAGGGCCCCCAGGG[A/C]CTCCTCATTCCTGCA | 267 |
| rs539539726 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364261 | AGGAACCACAAGCTA[A/C]GGATAATGGAGCAGC | 267 |
| rs539574491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392480 | AAAAAAGATTAGACG[A/G]ATGGCTAACTAGAAT | 267 |
| rs539659990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398537 | AGATCTCTACATGTT[G/T]CTTTGATAATTTAAC | 267 |
| rs539777223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397621 | AACATGGCACATGTA[C/T]ACATATGTAACAAAC | 267 |
| rs539824200 | snp | A/G | | | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424076 | TTTCTGATCACTGCG[A/G]GATTTACATAAGTAT | 267 |
| rs539903888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56391247 | GGTTCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 267 |
| rs539914200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391485 | GCACCTGGAAAATCA[A/G]GTCACTCCCACCCTA | 267 |
| rs539922464 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56376531 | TCAAAGACGATATCT[C/T]AGGATAAATTTTAAA | 267 |
| rs540040887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372251 | CTCCTATTTCGCCTC[A/G]CCTCGCCCCAGCCCT | 267 |
| rs540041149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364689 | TCCCCAGGCTCAGGG[G/T]ATCCTCCCAACTTAG | 267 |
| rs540099095 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56419714 | CAGGAGAATTGCTTG[A/T]ACCCAGGAGGCGGAG | 267 |
| rs540245796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391607 | GGGTCCCATGCCCAC[A/G]GAGCCTCGCTCGTTG | 267 |
| rs540287958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419109 | GCTCACTGCAACTTC[C/T]ACCTCCCAGGTTCAA | 267 |
| rs540309865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385307 | TCATTCACTCCAGCC[A/G]ATAATTCCCCAACAT | 267 |
| rs540366656 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402869 | ACTCCAGAGCCTTTC[C/T]TCTCCACCACTCTAT | 267 |
| rs540379735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391962 | AACTGCGAGGCACCC[C/T]CCAGTAAGGGCAGAC | 267 |
| rs540457417 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56406347 | AGGTCGAGGCAGGCC[A/G]ACTGCTTGATCTCAG | 267 |
| rs540473853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404272 | TTTCTTTCAAAAAGT[A/G]GACTTAGAAATGTGC | 267 |
| rs540497744 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56378655 | TCAAAAATAAGATGA[A/C]AAGCCAGATTGGGAG | 267 |
| rs540633510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56369966 | ACAAGTATGCATGGC[C/T]ATCCAGAGTGGAATG | 267 |
| rs540666846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410190 | AAAAAAAGAAAAAAA[A/T]GCTTACATTTTTAAT | 267 |
| rs540762679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402842 | AGTGGGGATTCACAC[C/T]CGGGCAGTCTGACTC | 267 |
| rs540818612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412189 | ATTTCTAGAACTTTA[A/G]GCACCCAAGAGCAAA | 267 |
| rs540883313 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426297 | TATTCGGCCATAAAA[A/G]TGAACTACTGATACA | 267 |
| rs540892137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363246 | GCACCAGGGAGGAAC[C/G]CTTCAGTGCTGTTCC | 267 |
| rs540895942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370519 | CATCTTGTTTATGAT[A/G]ATACACAATTATGTG | 267 |
| rs540896367 | snp | C/T | 0.00081501 | 0.0201703 | synonymous-codon | AMFR | GRCh38.p7 | 16:56362942 | CTGAAGCCTCCGTTC[C/T]GCGGCGGCAGCCAGC | 267 |
| rs540948903 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382611 | TGTCCTGGGCCACAT[A/G]CAGCCTGCAGGTTGG | 267 |
| rs540957456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363725 | ACAGTACCAGCATCA[A/G]AGGTAGACCAGTGGG | 267 |
| rs541094711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403316 | CTCCAATGCCAGTCA[A/T]CTTTCCTGAGAAACT | 267 |
| rs541115312 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417875 | AACATAACTGGAGCA[C/T]TCCTCATTTAAAAGC | 267 |
| rs541184207 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368065 | TAGTTCAGCCACCCC[C/G]AGAGGCAGCCCTCAA | 267 |
| rs541286835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381257 | CATGGGAAAGACCTG[C/T]CCCCATGATTCAACT | 267 |
| rs541326053 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56396582 | AACCATAAAAACCCT[A/G]GAAGAAAACCTAGGC | 267 |
| rs541356653 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427183 | ACGTTTGGCTTTACC[A/G]GGACAGGGAGAGGCC | 267 |
| rs541365753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374749 | TAAAAATATTAAGTC[C/G]TTTAAAGAAATTGAT | 267 |
| rs541466810 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56403481 | TAATTTCACTTATTA[C/T]ACTATATAACTACAT | 267 |
| rs541484397 | snp | A/G | 5.32193e-05 | 0.00515818 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362649 | TCGTCCCCCACCCCA[A/G]GCAGTCCAGTCAACA | 267 |
| rs541558542 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56423300 | GATGGAAGAAAAACA[A/G]CACTAGGATCAACTG | 267 |
| rs541669277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377458 | TCAGTAAACTAGGAA[C/T]AGAGGGAAACTTTGT | 267 |
| rs541704849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56417607 | CTGACCTCATGTGAC[A/G]AGTCGCAGTCAAAAT | 267 |
| rs541711497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418824 | AAAAAAAAAAGGAAA[C/T]ATGTGCACACACGTT | 267 |
| rs541731058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417142 | TGACCTGGCACAGTA[C/T]CTCGCACCTATAATC | 267 |
| rs541764427 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425235 | GAGCGCGCGGTAGGC[A/G]CTGATGATGGTGCCC | 267 |
| rs541886134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397272 | AGCAAAGACTTGGAA[C/T]CAACCCACATGTCCA | 267 |
| rs541908644 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56394722 | CAGTCCGCAGTCCGG[A/C]CTGGGCGACAGAGCG | 267 |
| rs541911780 | snp | A/G | 0.0047151 | 0.0483251 | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425329 | AAGAGCAGCGGCATG[A/G]CGGCAGCGGCGACCT | 267 |
| rs541945812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404025 | TGTCCCCTTTTTGAG[C/G]GGGGAGGGAGGCTTT | 267 |
| rs542016764 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362355 | CTCCTCTGCTCCAGG[C/T]ATCGAACCAAGAGTT | 267 |
| rs542123708 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371731 | TGTCAGTGTAAGTGA[A/G]CCCTCAGTACCACTA | 267 |
| rs542153039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368380 | GAGCTGAGAACTGGG[A/G]ACCACATCTAATATC | 267 |
| rs542157694 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56398356 | ATATATAATATATCA[C/T]TATATGATACACTAT | 267 |
| rs542158182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381394 | GTCTACATAAAAACC[C/T]GCACATAAATGTTTA | 267 |
| rs542195543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56389548 | GGACTTTACCTACTT[G/T]CCCTACTTCACTTTA | 267 |
| rs542258562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388639 | CCCTGTACAGCTGTC[A/G]AAAATATTTTCTTTT | 267 |
| rs542396573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373710 | GACAGCATGCAGGAA[C/T]AGACGGGCAGCATGA | 267 |
| rs542462230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409055 | AAAGAAGAGCTCCAC[A/G]AACCAGAGTAAGCTG | 267 |
| rs542645382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56366836 | CGGGCAGGGGGTGGG[A/G]GGAGGTGGCACCTCG | 267 |
| rs542678126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365335 | TTCCACTGACTCCAG[A/G]CAACACTGTGTGTGT | 267 |
| rs542732632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399781 | CTGTACACTTTAAAA[C/T]AGTTAAATGTATGTT | 267 |
| rs542766912 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388967 | AAAATAATGATAAAA[A/G]CTGTAGTAAATACCA | 267 |
| rs542827513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393363 | ATTCACACATAACAA[C/T]ATTAACCTTAAATGT | 267 |
| rs542899316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387279 | ATAATGGATTACATA[G/T]CCAGGTCTCATCTCT | 267 |
| rs542906573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56367223 | TCCAGCACATGAGGG[C/T]AATCCCCAGGGAATG | 267 |
| rs542919001 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | AMFR | GRCh38.p7 | 16:56395145 | AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT | 267 |
| rs542970331 | snp | C/G | 0.00318978 | 0.0398085 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361335 | CCTCCAACCAAAATA[C/G]TATACACAAAATCCA | 267 |
| rs543146892 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56399083 | TTAAGAATTATTACT[A/T]AAAAAAAAAACAAAA | 267 |
| rs543186320 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367274 | ACACAGGCCACACCA[A/C/T]GGGCACAGCCTGATT | 267 |
| rs543216177 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56402681 | AATCATGACAAATAA[A/G]AGCCTAATACTGAGC | 267 |
| rs543293654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379993 | CTTCTCATAGCTCCA[C/T]TAGGCGGTGCCCTAG | 267 |
| rs543394638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395970 | TAGGAATCCAACTTA[C/T]AAGGGATGTGAAGGA | 267 |
| rs543402286 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56368006 | GTGCTGGCTGGCCAG[C/T]GTCTGTATTTCATTG | 267 |
| rs543408044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413472 | GTGAGCTGAGATTGC[A/G]CCACTGCACTGCAGC | 267 |
| rs543436886 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361408 | CCTTAGCTTCCAGCC[A/T]CACAAAAACATGCCT | 267 |
| rs543491610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56386881 | AGGCGGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 267 |
| rs543539057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417532 | TCCAAAATCTGAAAT[C/G]CTCCAAAATCCAAAA | 267 |
| rs543565301 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363432 | CTGCTGTAGCTGCCA[C/T]CAACCATGGGTGTGT | 267 |
| rs543592086 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374824 | AAAGAAGGTATAAAT[A/G]AATAAAAACTGTTCT | 267 |
| rs543594564 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56400980 | TGTTGAGTTACCGAG[A/C]CTCTAGCTCCCATAT | 267 |
| rs543625522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56387475 | GGATTTCACCAACAC[A/G]ACACCATCCCCACTG | 267 |
| rs543691641 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56391712 | TTGAGTAGGTAAACA[A/C]AGCAGCCGGGAAGCT | 267 |
| rs543698478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56381164 | ATGGCAGCAGGCAAA[A/G]AGAGAGAGCTTGTGC | 267 |
| rs543719164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424338 | CAAAGGAAAACTGTC[A/C]TGAACATCAGGTAAA | 267 |
| rs543882635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56392618 | AAAGGGTATCAGTGA[C/T]TGAAGATCAAATGAA | 267 |
| rs543936995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393486 | GTGCAGTGACACACA[C/T]AGGCTCAAAATAAAG | 267 |
| rs543949291 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56388238 | ACAATCCTGTACAGC[A/G]TGTTACTATACTGAA | 267 |
| rs544003392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373748 | GATGGAAATCTTAAG[A/G]AAGAACCAAAGAGAA | 267 |
| rs544054074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56415774 | CCAGATCACCAGGAG[C/T]ATGGTGGCTCACACT | 267 |
| rs544065226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56422466 | CACCTCCTTCACCCC[C/T]GGTCTCCTCTTCACC | 267 |
| rs544120358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423787 | AGCAGTAGATAAACA[C/G]GAACTTCACCCTTCA | 267 |
| rs544182112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385765 | AACACAGGAATGTAA[A/G]TGGTCCCAGTAAATA | 267 |
| rs544195305 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | AMFR | GRCh38.p7 | 16:56417788 | ATTCCAAAATCCAGG[-/A]AAAAAATCCCAAATC | 267 |
| rs544242479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385358 | GCAGTGGCTCACGCC[C/T]GTAATCCAAGCACTT | 267 |
| rs544262448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413009 | ACCACCAAGTAATAC[A/G]TGTCAGCTCTAAACT | 267 |
| rs544315091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379391 | CAGGTCCCTCCCACA[A/G]AACGTGGGAATTCAA | 267 |
| rs544351089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370125 | CATGTAAGAAACCTG[C/T]ACTTGTAACCTGTAA | 267 |
| rs544367805 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382812 | TTCTTATTTTTTTCT[A/G]TCTGAAAAAGAGTAG | 267 |
| rs544402937 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56405785 | TCAAGCTTAGGAGTT[A/C]AAAACCAGCCTGGGC | 267 |
| rs544404152 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406248 | TTGCTATGTTGGCTA[A/G]GCTGGTCTTGAAGGG | 267 |
| rs544409686 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402317 | CTCCAGCCTGGGTGA[A/G]TGAGACTCCATCTCC | 267 |
| rs544410525 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56413829 | AGGCTTCTTTAAAAA[C/T]GACATTCCTAAAAGT | 267 |
| rs544446415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379821 | CAAGAGACGGGTTTC[C/T]GTGGTCTTGGGCAGC | 267 |
| rs544468290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372414 | TTGAAGTCTGAGTAC[C/T]ATTCTACTGTACAGG | 267 |
| rs544483199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407698 | TTCATGAATAGACCA[G/T]ATTTTTCCTTCAAAA | 267 |
| rs544508143 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56413409 | ATTCCCAGCTACTTG[A/G]GAGGTTGAAGCAGGA | 267 |
| rs544529980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365535 | AGGGAGATAGTTGGC[A/G]TAACATGTACACACA | 267 |
| rs544544569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414609 | AGCAGGCCACCTTAT[A/C]TTTCATCCTTAACTG | 267 |
| rs544545869 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56385681 | AGATCACAACAGAGT[A/G]AACCTAGTAGTGTTC | 267 |
| rs544584919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419275 | TGATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 267 |
| rs544614201 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56363806 | AGTTTTGGGGTGGCA[C/T]GTAATGCCGTTTCAC | 267 |
| rs544632769 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56415628 | TACATTTTTAAAGGA[C/T]TGAAACGAAAATAGT | 267 |
| rs544661219 | in-del | -/AAT | 0.0155029 | 0.0866667 | intron-variant | AMFR | GRCh38.p7 | 16:56402337 | CTCCATCTCCAAAAT[-/AAT]AATAATAATAATAAT | 267 |
| rs544663437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56423494 | AGAATCTGAACATGG[C/T]TTTTATCAAAATAAA | 267 |
| rs544666679 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377901 | AAATACATATAAGTT[C/G]TATATGAGGAAAATT | 267 |
| rs544697077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386641 | ACAAAAAGGCTTGTA[C/G]ACTAACAGCACCAAG | 267 |
| rs544727840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56370624 | TGCAAATTCCTTATA[C/T]GGCCCTGGAGCTGAG | 267 |
| rs544728258 | in-del | -/TA | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56398171 | TATAACTCTATCATT[-/TA]TATATATATAACTCT | 267 |
| rs544870481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391994 | GACACTTCACACGGC[A/G]GGGTACCCCTCTGAG | 267 |
| rs544871572 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56415440 | TAAAGAAGAAAGAAA[A/G]GGGATAGAGGAGAGT | 267 |
| rs544914123 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385620 | TCCAGAAAAAAAAAT[-/T]TTTTTTTTTTTTTGG | 267 |
| rs544932539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398286 | ATCATTTATATATGT[A/G]AATGTATCATTTATA | 267 |
| rs544978458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379875 | TACAGCCTCCCTCCC[A/G]GCTGCTTTCACAGAC | 267 |
| rs545005413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366773 | GAAGCGAATGGGAAC[C/T]ACAGAAGAGGAGTGG | 267 |
| rs545043654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379448 | AAACCATATCATTCC[A/G]CCCCGGCCCCTCCCA | 267 |
| rs545068032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365305 | CAGGGGAGCTGTGAC[A/G]GGAGCACGTTCACCT | 267 |
| rs545073084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56406789 | GCTAAAATAAAAGTA[C/T]ATACTATAGTATGAG | 267 |
| rs545091239 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56388549 | AATTTAGCTTACTAT[-/AA]GTTTTTTACTTCATA | 267 |
| rs545126174 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56413254 | ATGCCAGGCACAGTG[A/G]CTCACGCCTGTAATC | 267 |
| rs545128177 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386368 | CTCTAGAACCCTTCA[C/T]TGCTGAGCAATCCTG | 267 |
| rs545134497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405859 | TGGGCATGGTGGCAC[A/G]TGCCAGTAGTCCCAG | 267 |
| rs545182826 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407832 | ACACAAAAAGGAACT[C/G]AAATGCTTGTTAAAA | 267 |
| rs545360815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393321 | AACGAGCAAAATAAC[C/T]AGCTAACGTCATAAT | 267 |
| rs545385025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413277 | CTGTAATCCCAGCAC[C/T]TTGGGAGGCCAAGGC | 267 |
| rs545398087 | snp | A/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362448 | AGTCTACATGCTTCC[A/T]CAACAACGACAGCAG | 267 |
| rs545426848 | snp | C/T | 7.13559e-05 | 0.00597268 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362248 | TCACGGAAATCAAGC[C/T]GGCTTTGGACTGGAG | 267 |
| rs545441602 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372399 | AGGATTCCCTTCCTT[C/T]TGAAGTCTGAGTACT | 267 |
| rs545521071 | snp | A/C | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426647 | CCACCACACCTGGCT[A/C]ATTTTTAATTTTTGG | 267 |
| rs545624600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56391373 | GTGGGTGCAGCGCAC[C/T]GAGCATGAGCCGAAG | 267 |
| rs545635128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56385278 | GCCTCATAAAATTTT[C/T]AATAAAAGGCACATC | 267 |
| rs545638645 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387976 | ATTGACATGGAATCA[A/G]GCAAAATGCCTGGAA | 267 |
| rs545733070 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412258 | CCTAATTGATGCTAC[C/T]GGATGACATTAAACA | 267 |
| rs545735604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377935 | AAATCTTGATAAATG[A/G]TATCAACGAAGAATG | 267 |
| rs545854762 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427188 | TGGCTTTACCGGGAC[A/G]GGGAGAGGCCTTACC | 267 |
| rs545865522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391578 | CTCGGAGGGTCCCAT[A/G]CCCACGGCTCGGAGG | 267 |
| rs545966565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56397768 | TTATAATATATAAAT[A/G]TATCATTTATAATAT | 267 |
| rs545975205 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416570 | CCTGTATCAGCCTCC[C/G]AAGTAGCTGGGATTA | 267 |
| rs545997941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384442 | ATTTGTTCAATCAAT[C/T]AATAAAGATTAACTA | 267 |
| rs546054596 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370692 | GTAGGGCTCTAGGGT[A/G]GGTGTGTGTGTAGGG | 267 |
| rs546174238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382408 | TGTTTAATGGGTATA[C/G]AGCAAGGGTATCCAA | 267 |
| rs546196352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390430 | AGGAAAACCTCACCA[C/T]AATATGATAATCCTC | 267 |
| rs546213359 | snp | A/G | 0.000319022 | 0.0126257 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362776 | AGCTGTCCAAACACT[A/G]TAAGACCACATGCTT | 267 |
| rs546227099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56376516 | TAAATAACACATAGA[C/T]CAAAGACGATATCTC | 267 |
| rs546334210 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56411851 | TGCAGGGAAAGTACA[A/C]GGTGAACTTAGGACA | 267 |
| rs546371626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363217 | CCCCCAACAGATGGG[C/T]GCAAATTCTCTCTGC | 267 |
| rs546375421 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56418623 | GACCATCCTGGTTAA[C/T]TCAGTCAAACTCCAT | 267 |
| rs546417558 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56410834 | TTGCAGGGAGCCATG[A/T]TCATGCCACTGCACT | 267 |
| rs546451797 | snp | A/C | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56398162 | ATTTATAATATATAA[A/C]TCTATCATTTATATA | 267 |
| rs546464114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370947 | CTATAGAAGGAGCAG[A/G]GAGTATGTCAACGTC | 267 |
| rs546466041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363461 | GTGACGCACAGATGC[A/G]CTGAGTGTGTGTACA | 267 |
| rs546512185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411397 | ACATGACATCATGCC[C/T]GGCTAATGTTTTTTA | 267 |
| rs546529393 | snp | C/T | 0.000399281 | 0.0141238 | missense | AMFR | GRCh38.p7 | 16:56364105 | GTGGCACACGCTCGG[C/T]CTGGACACGGGGCAG | 267 |
| rs546580502 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418300 | CACGACGTCAGGAGT[C/T]CAAGACCAGCCTGAC | 267 |
| rs546735572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418968 | AGAGAAGCAGGTAAC[A/G]GGGAGAGAGAGAGAT | 267 |
| rs546809347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56412508 | CCAAGCCTGCCTGGC[C/T]TGACCAATTTCTGGT | 267 |
| rs546816424 | snp | C/T | 0.000107202 | 0.00732049 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362458 | CTTCCACAACAACGA[C/T]AGCAGTTTGATAACA | 267 |
| rs546974932 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56379756 | TCAAATCTTAAAGCT[C/G]CAAAATGATCTCCGC | 267 |
| rs546986632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402070 | AGGCCGAGCGCGGTG[A/G]CTTATACCTGTAATC | 267 |
| rs546986843 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56394603 | AAAAAATTAGCCGGG[A/C]GCGGTGGCGGGCGCC | 267 |
| rs547101057 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56410896 | CAAAAAAAAAAAAAA[A/T]TTGTGATGAATATTT | 267 |
| rs547107147 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399392 | ATTATTCACAATAGT[C/T]AAAATGTGGAAACAA | 267 |
| rs547151590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388858 | GCTGTCATCTCCTAG[A/G]ATAACAATACCTTAT | 267 |
| rs547156624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369414 | TGGCAGGCTTTGGGC[A/G]GTGAATGTGGCATCA | 267 |
| rs547243024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417858 | CAACCTATACTGAAA[A/G]AAACATAACTGGAGC | 267 |
| rs547287750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391403 | GCAGGGCAAGGCATC[A/G]CCTCACCCGGGAAGC | 267 |
| rs547306665 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425653 | CGCCTAGCGGGCGTA[G/T]CCCCGGGCCTCAGGC | 267 |
| rs547355991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390785 | CACTGTGACATACTT[G/T]TTATAAGCAAATCTA | 267 |
| rs547357863 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56397429 | AAACTATCACAAGGA[C/G]AAAAAGACACACACC | 267 |
| rs547374392 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56391953 | GAGTAGCCTAACTGC[A/G]AGGCACCCCCCAGTA | 267 |
| rs547400310 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422904 | GACCGATATTATTCT[A/G]AACTGTGCTCTAAAA | 267 |
| rs547403380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373316 | CTGGGGTCTGATCAA[A/T]GCTGCACCGACCGGA | 267 |
| rs547436882 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361575 | CAAGGTAAGGCTTTT[C/G]AAAGATTTATTGAAA | 267 |
| rs547510344 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56389894 | TTCCAACTCACTTAT[C/G]TGGCACCAAACTTAC | 267 |
| rs547547300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56387256 | TTTTAGTAGTCATAA[C/T]TCACAAAATAATGGA | 267 |
| rs547623294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380052 | CACATTTGCCTTCCG[C/T]ACTGCCGTAGCAGAG | 267 |
| rs547628197 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56375864 | AAGAGTTTGAGACCA[C/G]CCTGGCTAACATGAT | 267 |
| rs547661376 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56366373 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 267 |
| rs547662991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373922 | CCTGTAATCCCAGCA[A/C]TTCGGGAGGTCAAGG | 267 |
| rs547675191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367197 | CCCCGGGGAACACAA[A/C]CCCTTTCTCTTCCAG | 267 |
| rs547733530 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363684 | TCTCGGCAAGCGTGG[C/T]CAAAGGGGTCCATGG | 267 |
| rs547786217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56389062 | ATGGAGTGAAATGTC[A/G]TTATGGGGCACATGA | 267 |
| rs547823815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415031 | GAAAAGAAAACCGGC[A/G]AGAGGGGCCAAGAGA | 267 |
| rs547859029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382174 | GGTATATGCATACAA[C/T]GAAATATTACTCAGC | 267 |
| rs547922512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390029 | AATGTCCTCCACCCT[A/C]TTCTCTTTGCACGCT | 267 |
| rs547929860 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56423302 | TGGAAGAAAAACAGC[A/C]CTAGGATCAACTGAG | 267 |
| rs547967926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417967 | CAGGGGTTCGAGACC[A/C]GACTGAGCAACATGG | 267 |
| rs548160679 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56366770 | GAGGAAGCGAATGGG[A/C]ACCACAGAAGAGGAG | 267 |
| rs548172128 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371571 | GCGACCACACTCCCA[A/G]GCCACCTATATGCAC | 267 |
| rs548173541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396087 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 267 |
| rs548186631 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56367051 | ATCTCAATGGCCTCG[A/G]CTCCCTGGAGAGCTT | 267 |
| rs548307102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380703 | CTTAAGGCAGGGGCA[A/G]CATGCTGCCATTCTC | 267 |
| rs548309845 | in-del | -/AAATACAAAATACATAA | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56403864 | TAAAAAGAATCAGTT[-/AAATACAAAATACATAA]AAATACAAAATACAT | 267 |
| rs548375468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369443 | CATGCCCTGAAAACA[C/G]AGGTAAGGGAGCCAC | 267 |
| rs548441569 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374096 | ACTGCTTGAACTCAG[A/C/G]AGGTGGAGGTTGCAG | 267 |
| rs548576093 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56374892 | CATTCAGTTATGTGT[G/T]CTTGTGCACGTGTGT | 267 |
| rs548603471 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424296 | GCTGCCTCTTGACAC[C/T]GTGAATGTTTTGCTG | 267 |
| rs548631033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402193 | ATGCAAAAATTAGCC[A/G]GGCGTGGTGACAGGC | 267 |
| rs548638942 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370233 | TTAAAGATATAATTC[C/T]TAAAGGGAACAAACT | 267 |
| rs548652457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417183 | CGGAGGCCAAGGTGG[C/G]GGGATTGCTTGAACT | 267 |
| rs548654360 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56408654 | CAACTCCTGAGGTCA[C/T]AGGCGGAGATTAAAA | 267 |
| rs548767315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400288 | TTACAGGCACCTGCC[A/G]CTTTGCCCAGCTAAT | 267 |
| rs548788941 | snp | A/G | 3.34499e-05 | 0.00408948 | intron-variant | AMFR | GRCh38.p7 | 16:56409414 | GCAAAAAGCTTGGCT[A/G]AAAACTCACATATTC | 267 |
| rs548832238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402898 | ATTAGCAGTTTACAA[A/G]CATACATTCTGACAT | 267 |
| rs548850899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373259 | CACTGTTCTTAACAA[C/T]GTCTGCCCTCAGGAG | 267 |
| rs548900314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56418536 | AAAAAAACGCCAGGC[A/G]CACTGGCTCACACCT | 267 |
| rs548936506 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56407276 | TTTATCTAATATCTC[A/T]TTTTTTAATTAATAA | 267 |
| rs548968651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391748 | TGAGTGGAGCCCACC[A/G]CACCTCAAGGAGGCC | 267 |
| rs549024506 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56386162 | TGCCAAGTGTTTCAC[A/G]TGGACTAGCTCATTT | 267 |
| rs549042166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385415 | AAGGCCAGGAGTTCG[A/G]GACCAGACTGGCCAA | 267 |
| rs549092478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56399621 | AGACAGAAAGTGGAT[C/T]AGTGGTTGCCAGGTG | 267 |
| rs549105912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392370 | CTGGACAGAGAATGA[C/T]TTTGACAAGTTGAGA | 267 |
| rs549144412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421272 | CAGCCCTTAAGTTTT[A/T]TAATAATACGAAAAT | 267 |
| rs549194396 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56382647 | CTTGGTACAAAGTTT[C/T]GATTGTGCAAGATGA | 267 |
| rs549201158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393765 | AATAATAATGGGAGA[C/T]TTTAACACCCCACTG | 267 |
| rs549216283 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414202 | TCATAATACAAAGTT[A/T]AAAAAAAAAAATCTA | 267 |
| rs549276908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387765 | TTTTATGGACAAAGC[A/T]ACAGGGTTCCAGCTC | 267 |
| rs549281380 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56421939 | CAAATCCTTTCTCAA[G/T]GTCATGCCTGAGGGC | 267 |
| rs549323141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372686 | GATGTGCTTTCGAAT[C/T]TACCCTTAAAAAACA | 267 |
| rs549338113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387059 | TTGAGATCACGCCAC[C/T]GCACTCCAGCCTGGC | 267 |
| rs549365162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408537 | AGTCTATTAGGGCTA[C/G]CACAATTGAAATGCA | 267 |
| rs549497820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401384 | CTCCCAGTTAGATAA[C/T]AAGCTGTCTGAAAGC | 267 |
| rs549529735 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390393 | TAAATATCTACGAAC[A/T]TGTGTAGATATAAAG | 267 |
| rs549765839 | in-del | -/TG | 0.00159617 | 0.0282053 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426233 | TGGGAACAACGCTAA[-/TG]TCCGTCAAGCGATGA | 267 |
| rs549770148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385491 | CCACGCCTATAATCC[C/T]AGCTACTCAGGAGGC | 267 |
| rs549804434 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | AMFR | GRCh38.p7 | 16:56411472 | TGGTCGCAAACTCCT[A/G]GGCTCAAGTGATCCC | 267 |
| rs549843694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379674 | AATACAGCTGTTCCA[A/G]ATGGGAGAAATTGGC | 267 |
| rs549904887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56386124 | GGTGTTCACTGAGGG[C/T]TTCTTGTATGGCAGG | 267 |
| rs549911616 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392966 | GGGCAGCAAGAGAGA[A/C]AGGTCGGGTTACCCA | 267 |
| rs549966374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421626 | CGTATCTTGCTCTTA[C/G]AATTTTAGAAGCAGA | 267 |
| rs550022870 | snp | A/G | 3.31115e-05 | 0.00406874 | missense | AMFR | GRCh38.p7 | 16:56408017 | TGTAGCCGGTGATGG[A/G]GCAGACGGCCGCCAG | 267 |
| rs550058235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424004 | GGGAACATGCAAGGA[A/G]ACAAGATCCAAGAAG | 267 |
| rs550111984 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56422195 | ACATGACATCACACT[C/G]TAGCCTCTTCCTAGG | 267 |
| rs550144490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380782 | TCCTCATCTCCATTT[A/G]AGACCACCTCAGCCT | 267 |
| rs550167764 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | AMFR | GRCh38.p7 | 16:56372062 | TGTCCCACTTTATAT[C/G]AGAGACTTGAGCATT | 267 |
| rs550168012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56364206 | CACGGCTGTTCTGGA[C/T]GCAAAGAGAAGGCTG | 267 |
| rs550231098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56414996 | GGCACTGCAGCAGGG[C/T]GGAATGGGTTAAACA | 267 |
| rs550251559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373115 | ACTCAGGCAGAGGTG[A/G]CTCCCCTGTAATACT | 267 |
| rs550365412 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56416615 | ACACTAATTTTTGAA[-/T]TTTTTTTATAGAGAC | 267 |
| rs550398384 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56422006 | GGTCACTAGATCTCC[C/T]GTCCTCTTCCCACTC | 267 |
| rs550426882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420909 | AGAACCTTGACAGTA[G/T]TTTCATATTTCTATT | 267 |
| rs550431152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372721 | CCTGACACAGTGGCT[C/T]ACGCCTGTAATCCCA | 267 |
| rs550495119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365680 | CAGGTTAGAAAAAAT[A/G]GTGAGTGAAGAGGCG | 267 |
| rs550504509 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56399634 | ATCAGTGGTTGCCAG[A/G]TGATGGAGAAGGAAG | 267 |
| rs550537993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419701 | TGGGTGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 267 |
| rs550550824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411546 | CATGTAAATGTTTCA[A/C]AAATTCAAAAAATAA | 267 |
| rs550567721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399193 | AGTATGAAGAAACTA[C/G]ACCCCTCAGGTATTG | 267 |
| rs550654519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405337 | AACATTTCTCAGTTC[A/C]ATTAAAAAGCAGATT | 267 |
| rs550690059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403630 | ATGTAAAATGTGAAA[C/T]AGCAAACAACCAAAT | 267 |
| rs550698317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370973 | ACGTCAGGACCTTGA[A/C]GGAAAAGGTCGGCAC | 267 |
| rs550714770 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56403194 | GGCGCAGTATGCAGC[A/G]GAAGCTCTTCACTGT | 267 |
| rs550826073 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397134 | CGATTCCTCAGGGAT[C/G]TAGAACTAGAAATAC | 267 |
| rs550885206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398489 | TGAAATGTAGAGATA[C/T]ATGTGTATATACATA | 267 |
| rs550891265 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391016 | CAGCAACAAATTATC[C/T]AGCTATTGTGCCTGC | 267 |
| rs550914174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377744 | CACTCTTGGAACTAA[C/T]AAGCAATTACAGCAA | 267 |
| rs550943374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421859 | AGTTTTAGAAAGACA[A/C]GGAGAAACAAATTCT | 267 |
| rs551006726 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56421197 | TCAAGCAATCCTCCA[A/C]CTCCTGCCTCAGCCT | 267 |
| rs551030866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391652 | TGTGATTGAACTGCA[A/T]GGTGGCAGCGAGGCT | 267 |
| rs551068626 | snp | G/T | 5.22161e-05 | 0.00510934 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362875 | GTCAGTCGGGCACAG[G/T]GCGCAGGAGGCAGCT | 267 |
| rs551071812 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377094 | TCTCTTTCAGAGGAC[A/T]GAAGCAGAAGGGATA | 267 |
| rs551081022 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379925 | CTTTTCCAGGCACAC[A/G]GTGCAAGCTGTCAGC | 267 |
| rs551083300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404381 | CTCACCATTATTAGA[C/T]CACTGAAGGGCCAAC | 267 |
| rs551166112 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406528 | ACTGCACTCCAGCCC[A/G]GGCAACAGAGTGACA | 267 |
| rs551177865 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56412380 | CCTCTGGATCTAGTT[-/A]AAAAAATCTCTAAAA | 267 |
| rs551208592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413973 | TGTGCTGTAAAAATG[C/T]CTTTGCTCTTAGAAA | 267 |
| rs551275354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56384666 | TTGAGCCAACAGCAC[A/G]CCTCAACATTTCAAG | 267 |
| rs551360660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56397694 | AATACATACATATAT[C/T]TTATATATAATCATT | 267 |
| rs551360963 | snp | A/C/G | 8.26076e-05 | 0.00642634 | stop-gained, synonymous-codon | AMFR | GRCh38.p7 | 16:56405038 | CCAGAGGTGAATTAC[A/C/G]TATCTGTAATGAAGA | 267 |
| rs551497235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364977 | ATGCCCAGGCACCCC[A/C]AGGTCCTAGCAGGTG | 267 |
| rs551542733 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56372560 | CCATCCCTCCTCACA[A/C]CCCTCTCTCCTACTC | 267 |
| rs551599515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399432 | CCACCAATGGATGAA[C/T]GGATAAACTAATTGT | 267 |
| rs551690710 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56392193 | AAACAGAAAGGACAT[C/T]CACACCAAAACCCCA | 267 |
| rs551736986 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56393088 | GAAAAGAATTTTCAA[C/G]CCAGAATTTCATATC | 267 |
| rs551825817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56391729 | GCAGCCGGGAAGCTC[A/G]AACTGAGTGGAGCCC | 267 |
| rs551832520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385388 | TTGGGAGGCCAAGGC[A/G]GATGGATCACTAAGG | 267 |
| rs551835231 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426897 | CGAATTGTATCTCAA[C/T]AAGCTGTTACCAAAG | 267 |
| rs551958055 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56378258 | TAGATCAATGGAACA[C/G]AATAGAGAGCCCAGA | 267 |
| rs551992730 | in-del | -/ACCCATAG | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56416830 | TCTTATAATCCCATC[-/ACCCATAG]AACAACCACTTCCTA | 267 |
| rs552014838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404492 | ATTAAGTGTAAAGAC[C/T]TTTTTTAATTACAAA | 267 |
| rs552144570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412371 | ATTATAATTACCTCT[A/G]GATCTAGTTAAAAAA | 267 |
| rs552159988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390716 | TAGTATAATAAAATT[A/T]GCCTTGTGGGAGATT | 267 |
| rs552178167 | in-del | -/A/AAAA | 0.498133 | 0.030494 | intron-variant | AMFR | GRCh38.p7 | 16:56406552 | GTGACACCTTGTCTC[-/A/AAAA]AAAAAAAAAAAAAAA | 267 |
| rs552256924 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373519 | CCACAGTCCTTTTTA[C/T]GCAGTACATCATGTT | 267 |
| rs552280933 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56419793 | GAAAGACTCTGACTC[-/A]AAAAAAAAAAAAATT | 267 |
| rs552293734 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361787 | AAAAAAAAAAAAAGT[A/C]ATCCAATGGGGCATA | 267 |
| rs552308963 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426701 | GTCCAGACCAGTCTG[G/T]GGCTCCTGAGCTCAA | 267 |
| rs552352687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363410 | CCCCTCTATCCACAG[C/G]ACACACCTGCTGTAG | 267 |
| rs552465079 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56411753 | ATGAGCACACTCAGC[A/C]AGTATACAGCTTGGC | 267 |
| rs552487659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370215 | TATAAAAATGTGTTT[G/T]CCTTAAAGATATAAT | 267 |
| rs552528575 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425521 | GCTCCCGCTGCTGCC[C/T]CTGCCGGCGCGGAAG | 267 |
| rs552549381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368434 | GCTCTTTCCTCTTCA[A/G]AGAGTCTCAGGTTTT | 267 |
| rs552560514 | snp | A/G | 2.80871e-05 | 0.00374737 | intron-variant | AMFR | GRCh38.p7 | 16:56363098 | TCTCATAGGAGAGAT[A/G]GGGAGCTGTGGAACA | 267 |
| rs552566107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56390045 | TTCTCTTTGCACGCT[A/G]TTTTCCCAACAAGGC | 267 |
| rs552627102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396120 | GCCCAAGGTAATTTA[C/T]AGACTCAGTGCCATC | 267 |
| rs552663060 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417812 | CCAAATCCAAAACTT[C/G/T]GGGTCCCAAGCATTT | 267 |
| rs552666273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402239 | TACTCAGGAGGCTGA[A/G]GCAGGAGACTTACTT | 267 |
| rs552666357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410347 | ACTTGCCAGCCCATA[A/G]TAAAGGCGGCATAAA | 267 |
| rs552684791 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56375065 | TTGCAAATGTATATT[A/G]CAAACTCTAGGGCAA | 267 |
| rs552697974 | snp | A/G | 8.87083e-05 | 0.0066593 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362618 | TGCAGGCAGGCGACT[A/G]CTCACTTCCTCCTGA | 267 |
| rs552699926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369727 | ATATGTTTATTGCAG[C/T]GCTATTCACAGTAGC | 267 |
| rs552723685 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56409782 | GAGGTAAGACACCCA[A/G]AAACTAATCTGTAAA | 267 |
| rs552748164 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56397993 | ATATATAAATGTATC[A/G]TTTATAATATATAAA | 267 |
| rs552748194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375729 | ATTACAAAATGATCA[C/T]GGGGTCAATTCTCCA | 267 |
| rs552780233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377007 | TTCCACAGCAGAAGG[C/T]ATCAGCCCACATGAG | 267 |
| rs552799092 | snp | A/G | 1.64749e-05 | 0.00287005 | missense | AMFR | GRCh38.p7 | 16:56403028 | GATAGTTCTTGTGCC[A/G]ACGAATTCGACGTTG | 267 |
| rs552804595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396962 | CCATCAGAGAAATGC[A/C]AATCAAAACCACAAT | 267 |
| rs552812271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391556 | GGAGATTATATCCTG[C/T]GTGTGGCTCGGAGGG | 267 |
| rs552880337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404554 | AACACTGCAGGAATT[C/T]CCATTACCACCTACA | 267 |
| rs552936390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403508 | ACATATTACTATTAT[A/G]TTTGTATATATAACA | 267 |
| rs552981095 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418472 | TCATGCCACTGCACT[C/T]CAGCCTAGGTGACAG | 267 |
| rs553042374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56418010 | TCTACTAAAAACACA[A/G]CAAATGTAGCCAGGC | 267 |
| rs553042725 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426748 | GCCTTCACAAAGTGC[A/T]GGGATTACAGGCGTG | 267 |
| rs553045194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56411172 | ATAGACTATCAAGCC[A/G]TCTAGGGGGGTCAGG | 267 |
| rs553205876 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368168 | ATCCCAGAGGCCCCA[A/G]ATGGGAAGGGGCTTG | 267 |
| rs553409110 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361983 | GCTCCCAGGATAAAA[G/T]ATACAAAAGTTCTTT | 267 |
| rs553452398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423552 | ATACCAGTGTTGTTA[C/T]ATAAATAAAATAAGG | 267 |
| rs553469089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396170 | TTTTCTTCACAGAAT[A/T]GGAAAAAACTACTTT | 267 |
| rs553469187 | snp | C/T | 1.77153e-05 | 0.00297612 | intron-variant | AMFR | GRCh38.p7 | 16:56389410 | AAGATACGTCAGCAT[C/T]CTTGATTGTTCCTTA | 267 |
| rs553530174 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56416663 | CCCAGGCTGGTCTCG[A/T]ACTCCTGGGCTCAAG | 267 |
| rs553530306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395606 | CTGGAAGCATTCCCT[C/T]TGAAAACGGGCACAA | 267 |
| rs553555842 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56376159 | AAAATTAAAAGAACC[A/G]CAAAGAGAAACAAAA | 267 |
| rs553604197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390253 | CCTCTATTGACTAGT[C/G]CTCTCCACTAAAGAA | 267 |
| rs553610153 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56392757 | TGTACCTGAAAGTGA[C/T]GGGGAGAATGGAATC | 267 |
| rs553622967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380298 | ACAGGGCACCAAGTA[C/T]CTAGGCTGCACACAG | 267 |
| rs553669267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417324 | CTGAGGTGGGAGGAT[C/G]TCTTGAGCCCAGGAG | 267 |
| rs553705483 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425865 | CCCCCACCCCATTAA[A/C]CCTCTGAAGAGGTTA | 267 |
| rs553759426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391411 | AGGCATCGCCTCACC[C/T]GGGAAGCGCAAGGGG | 267 |
| rs553761311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379735 | GTCCAAAATAAGGTA[A/G]GGCAGTCAAATCTTA | 267 |
| rs553805086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380879 | CCAAACTTTCCCACA[G/T]TTTCCTGTCTTCTCC | 267 |
| rs553827782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56373677 | ATTAATATGCAAAGA[A/G]CACTAATGGATAAAG | 267 |
| rs553837330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372206 | AACTTTTTCATCTTG[C/G]AAAACTGAAACTATA | 267 |
| rs553895152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365789 | GGGGCAGGGCAGAGA[G/T]TAGAACAGAGGGAGA | 267 |
| rs553917044 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413330 | AGTTTGAGACCAGCC[C/T]GGCCAACGTGGCGAA | 267 |
| rs553930178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407495 | CAAGCAATTCTCCTG[C/T]CTCAGCTTCCCAAGC | 267 |
| rs553935221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399772 | GCAACTGAACTGTAC[A/G]CTTTAAAATAGTTAA | 267 |
| rs554058508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401910 | ACTAAACACCACTTG[A/C]TAGACTGCGCCTGTA | 267 |
| rs554071657 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393329 | AAATAACCAGCTAAC[G/T]TCATAATGACAGGAT | 267 |
| rs554071736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400782 | CCTTTGCTTTAAAGC[A/G]CTTATCTCATTGATA | 267 |
| rs554095389 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56374372 | CACAGATCCAGGAAT[C/T]TTAGAGAGTACCAAG | 267 |
| rs554117168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413643 | TCTGAGTCACTTTCC[A/C]ATGTCAGACAATCTC | 267 |
| rs554149171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381097 | CCACATGGCTGGGGA[A/G]GCCTCATAATCATGG | 267 |
| rs554226409 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56374527 | CTTTTAGAGGAGCAA[A/C]GTTAGGAATGACATC | 267 |
| rs554248584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421379 | TCCTTAATTTATTTA[A/T]TTTGTTTTACAACCC | 267 |
| rs554335643 | snp | C/T | 0.00139449 | 0.0263685 | missense | AMFR | GRCh38.p7 | 16:56408080 | GGGACAGGACTCGAC[C/T]GTGGCTGCTCATCGG | 267 |
| rs554390536 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56417438 | ATAAATAATATTGTG[C/T]CATACATATAACTTC | 267 |
| rs554445345 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419519 | CAACTATGGCCAGGC[A/G]TGGTGGCTCATGCCT | 267 |
| rs554588467 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56402479 | TGTCCCCCTGGGTGC[A/C]AAGAGGATACCCATT | 267 |
| rs554691115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366479 | AATTACATAGGTGGA[C/T]ATGAAAATCTTAACC | 267 |
| rs554733929 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56393979 | GCACTTCTCAGCAAA[A/T]GTAAAAGAACAGAAA | 267 |
| rs554763159 | in-del | -/AAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56416838 | TCCCATCACCCATAG[-/AAC]AACCACTTCCTATTT | 267 |
| rs554811208 | snp | C/T | 1.77634e-05 | 0.00298017 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362534 | CCCACACTCTTCCCA[C/T]TGGGTGTGGTGCTCA | 267 |
| rs554811335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56388075 | AAATACAGTCAATGC[A/G]TAGCTTAACAACAGG | 267 |
| rs554832650 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56367977 | GGACCAGCCAGTAAG[A/G]TCTCGCCACCTCAGT | 267 |
| rs554873106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387352 | TTCATTCACAGCCAC[C/T]AAACCAGGTCCTCTA | 267 |
| rs554927450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407585 | AGAGACAGGGTTTCA[C/T]CATATTGGCCAGGCT | 267 |
| rs554950003 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56396009 | CAAGGAGAACTACAA[A/G]CTAATGCTCAACAAA | 267 |
| rs554979160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415162 | ATGAATATCCTTACA[C/T]CTAAACGCCAAATCT | 267 |
| rs554986763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423388 | CCTCTACTGAAAATG[C/T]TGGAAGAAAAGGAAA | 267 |
| rs555031434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373401 | AAGTAGATTGAAGTT[C/T]ACAGTCCAGAGCATG | 267 |
| rs555060084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398683 | AACATATCCAAACTT[A/C]TGAGATGCAGCGGAA | 267 |
| rs555136097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401559 | TAGGGAAGAGGCTAA[C/G]GAACAAAGAAGGATA | 267 |
| rs555272746 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | AMFR | GRCh38.p7 | 16:56394691 | GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG | 267 |
| rs555294265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372847 | AAAAATTAGCCAGGT[A/G]TGGTGGTGCATGCCT | 267 |
| rs555467705 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56385715 | AAAGGTTAGATTATC[C/T]GCCACAGAAATAAAA | 267 |
| rs555469702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393201 | GTCTGCCCTAAGAGC[C/T]CCTGAAGGAAGCACT | 267 |
| rs555487188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401214 | TACTTCCATCTGGAA[G/T]GATTACAGAAGAGAC | 267 |
| rs555518275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412851 | GTGACAGAGCAAGAC[A/G]CTGTCTCAAAAGAAA | 267 |
| rs555532401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392563 | CGAGAACTACGTGAC[A/G]AATGCACAAGCTTCA | 267 |
| rs555542194 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56379327 | ACTTATTCACTATCA[C/G]GAGAACAGCAGGAGA | 267 |
| rs555619573 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56384993 | TTTTAGTAGAGACAG[C/G]GTTTCACTATATGGG | 267 |
| rs555682234 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387645 | AGCTTAATGTGAATT[A/G]AGGAAGGATGATCAA | 267 |
| rs555735079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384191 | TCAGAGAGAACATCT[C/T]CAAATGCCTCCTCTA | 267 |
| rs555781333 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56415113 | CTATGAGAAAACTTG[-/A]AAAACAAAACAAAAC | 267 |
| rs555890143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383766 | CTGTCCAAGCCCCCA[C/T]GTGAATTTCCCTTGA | 267 |
| rs555968677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408659 | CCTGAGGTCACAGGC[A/G]GAGATTAAAAAAAAC | 267 |
| rs555980656 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56398279 | TAACTGTATCATTTA[C/T]ATATGTAAATGTATC | 267 |
| rs556006336 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56365195 | TCAAGAGAACCATTC[A/G]TATCCCCGAGAGTCA | 267 |
| rs556035343 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411171 | AATAGACTATCAAGC[C/T]GTCTAGGGGGGTCAG | 267 |
| rs556039813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405672 | ACTCCCTTTGTCCAC[C/T]AGCAGAAAAAAGAAC | 267 |
| rs556056053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56423491 | TTTAGAATCTGAACA[C/T]GGCTTTTATCAAAAT | 267 |
| rs556080066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371412 | CTAAACAACTCCCAG[A/C]AGGGAATTCTGATTC | 267 |
| rs556111925 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415362 | GCCTCTGATTCACTA[C/T]GTTTACCATATTACC | 267 |
| rs556119694 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415584 | TTTAGTTCTATTCTG[C/T]CTGCCTAATGGGCCA | 267 |
| rs556145315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56364404 | AAACGTAAGCACCTT[C/T]AAGCTGCACTCTTAG | 267 |
| rs556156679 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56412841 | TCCAGCCTGGGTGAC[A/C]GAGCAAGACGCTGTC | 267 |
| rs556190956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415348 | GTAAAGCTGCTTCTG[C/T]CTCTGATTCACTACG | 267 |
| rs556232152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378539 | ATAACCTAGGGTATG[A/G]CAATGACTTTTTAGA | 267 |
| rs556265297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56379822 | AAGAGACGGGTTTCC[A/G]TGGTCTTGGGCAGCT | 267 |
| rs556283158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379026 | CTCTGGAGGATGATT[C/T]GGCAGCTTCTAACAA | 267 |
| rs556328632 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56386610 | ATTCAAAATTCTTTT[A/T]AAATTGTTCTATTCT | 267 |
| rs556393058 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56421301 | ATCGGCTCTTTAAAA[C/T]AGGATTCAGCCAATT | 267 |
| rs556415111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372923 | CCTGGGAGGTGGAGG[C/T]TGCAGTGAGCCAAGA | 267 |
| rs556443260 | in-del | -/AATC | 0.00716266 | 0.059414 | intron-variant | AMFR | GRCh38.p7 | 16:56376735 | CAGAAGAAAACAAAT[-/AATC]AAAATGAGAGCAGAC | 267 |
| rs556464421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407412 | TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG | 267 |
| rs556501009 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388090 | GTAGCTTAACAACAG[A/G]GACACATTCTGAGAA | 267 |
| rs556537291 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56399686 | TGACTATGGGGCACT[A/G]TTGTGGAGTGATAAA | 267 |
| rs556537776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364496 | TAATTGCTCAAACAT[C/T]TAAACCAGTCTTATC | 267 |
| rs556556515 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425894 | TACCCCCAGCACTCC[C/T]AGGGGCCGCGCAGCT | 267 |
| rs556602026 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56394139 | AATGAAGGCAGAAAT[-/A]AAAGATGTTCTTTGA | 267 |
| rs556622838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56363186 | CTCAGCACCACCCAA[C/T]GACCAAGACATCCAG | 267 |
| rs556626737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390787 | CTGTGACATACTTTT[C/T]ATAAGCAAATCTAAA | 267 |
| rs556684505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363628 | GAGCTGTTAAAGTAA[C/T]TCATATAAAGGGCTT | 267 |
| rs556731050 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56419030 | CTTAACTTTTTTTTT[C/T]TTTTTTAATTTTAGA | 267 |
| rs556750600 | snp | A/G | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56409586 | AAATTTGTCTTTGAG[A/G]TGCTAAAAAAGAAAA | 267 |
| rs556774608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392717 | TATGGGACTATATGG[A/G]AAGACCAAATCTATG | 267 |
| rs556806884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385152 | CACCCAGGCTGTAGT[A/G]CAATGGTGTGAGCAC | 267 |
| rs556835964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398836 | GGTATCTAGAGTAAT[A/T]CATAGAGTCAAAAAA | 267 |
| rs556979051 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56404184 | GATTACAGGCATGAG[A/C]CACCGCGTCCAGCCG | 267 |
| rs557113118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56391565 | ATCCTGCGTGTGGCT[C/T]GGAGGGTCCCATGCC | 267 |
| rs557113897 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56404657 | TAATCTATTGACTTG[C/G]TCAGCAGAGTTAACT | 267 |
| rs557288376 | snp | A/C/T | 5.00513e-05 | 0.00500231 | intron-variant | AMFR | GRCh38.p7 | 16:56401873 | CAAGCCCAGCAGGAA[A/C/T]CTCAGTCAGTTCCAC | 267 |
| rs557299692 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56400357 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 267 |
| rs557343254 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385550 | AGGTAGAAGGTGCAG[C/T]GAGCCAAGATCGCAC | 267 |
| rs557364565 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56376444 | TTAAAGCAGAAATCA[C/T]TAACAGTAAGAAAAC | 267 |
| rs557433202 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56383000 | TGACCTATTCAAAAA[-/C]CCTTAAACAAACGAA | 267 |
| rs557439512 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56376088 | TTAAATAAATAAATA[A/C]ATTTAATAAATAAAG | 267 |
| rs557458981 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56390862 | CCTAAAAACTCCAAG[A/G]TGAGTACAACTAGTT | 267 |
| rs557459109 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56382352 | AGCAAGTAGCATAAT[A/G]GTTGCCAAAGGCTAG | 267 |
| rs557486993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377039 | TCGCTAGTGAATTCT[A/G]CCAAACATTTAAGGA | 267 |
| rs557520327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390388 | TCTTTTAAATATCTA[C/T]GAACATGTGTAGATA | 267 |
| rs557604353 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379251 | ACATGGATGGTGGCA[C/G]GCAAAGAGAGAGAGC | 267 |
| rs557606810 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56378775 | CCTGATCAAAAAATG[A/G]GTATAAGATCTTAAT | 267 |
| rs557665917 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56392528 | CCTTAAAGGACCTGA[C/T]GGAGCTGAAAACCAT | 267 |
| rs557771162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405439 | CAACTTTTATTGAGG[A/T]AAAGTCCTGTTAATA | 267 |
| rs557793483 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416685 | GGGCTCAAGTGATCC[A/G]TCTGCCTCGGCCTCC | 267 |
| rs557795008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56391918 | GACAGACTGCCTCCT[C/T]AAGTGGGTCCCTGAC | 267 |
| rs557805268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385562 | CAGTGAGCCAAGATC[A/G]CACCACTGCACTCTA | 267 |
| rs557847117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398592 | TAAACTATAGTTTAC[C/T]TGTAAATATACAGAT | 267 |
| rs557932144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385291 | TTTAATAAAAGGCAC[A/C]TCATTCACTCCAGCC | 267 |
| rs557943392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384113 | CACCTACTGTTTCCA[C/T]GGCCTCCTTCCCCCT | 267 |
| rs557985968 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56373506 | ACAGGCCTGTTCACC[A/G]CAGTCCTTTTTACGC | 267 |
| rs558005022 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56391491 | GGAAAATCAGGTCAC[C/T]CCCACCCTAATACTG | 267 |
| rs558084901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56376021 | CGAGATCGGGCCACT[A/G]CACTCCAGCTTGCGC | 267 |
| rs558109970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418639 | TCAGTCAAACTCCAT[C/T]TCTACTAAAAATACA | 267 |
| rs558221920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375445 | CAGTAACAAAATGGT[A/T]GTTATTAATCCAAAT | 267 |
| rs558230782 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406740 | ATCAAATCTGTAATA[C/T]GATAAATTATCTTAA | 267 |
| rs558238651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417551 | CAAAATCCAAAACTT[C/T]CTGAGCACCAACATG | 267 |
| rs558266154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383461 | CAATCTCCCAAATGT[A/G]CATCTCTCACTTGAT | 267 |
| rs558285710 | snp | C/T | 0.00021796 | 0.0104371 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362198 | AGGGGAGGGGACCCA[C/T]GGGGCACACTCATGA | 267 |
| rs558309155 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56393582 | TGACAAAACAGACTT[C/T]AAACCAACAATGGTC | 267 |
| rs558315956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403247 | CTTTCAGAAAGGAAA[C/T]ACACAGATTTATCTC | 267 |
| rs558344188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56363711 | ATGGGAGATGACTGA[C/T]AGTACCAGCATCAGA | 267 |
| rs558392349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397179 | ATCCCATTACTGGGT[A/G]TATACCCAAAGGAAT | 267 |
| rs558446679 | snp | A/G | 1.67851e-05 | 0.00289694 | intron-variant | AMFR | GRCh38.p7 | 16:56404888 | TTGCCCTCTGTTAGA[A/G]CTCCTTCTGAGGAAA | 267 |
| rs558455332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411072 | CACTGTACTCTTTTA[C/T]ACAGAGGGCTTCCAG | 267 |
| rs558480099 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56369923 | AGAAACTCAAATACC[A/G]TATGTTCTTATAAGT | 267 |
| rs558535051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56390447 | ATATGATAATCCTCA[A/G]AGTCTCCAGCAACTA | 267 |
| rs558538948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56369057 | TATTAATTTGGGAAA[C/G]TTAGAGAGTTTATAG | 267 |
| rs558617993 | snp | C/G | 0.000399281 | 0.0141238 | missense, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425184 | CAGCGAGGCCGTTAG[C/G]TGGTCCGGCTCGCCG | 267 |
| rs558619605 | snp | A/C | 1.67674e-05 | 0.00289541 | missense | AMFR | GRCh38.p7 | 16:56362989 | TCACGGGGTCAGAGG[A/C]CGCACCTTCCGAGGG | 267 |
| rs558642252 | in-del | -/CT | 0.00636936 | 0.0560724 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425767 | GCGGCGCAGGGGTCA[-/CT]CGGGCTCGCAGGCGC | 267 |
| rs558743738 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56394886 | CAAACTACCATCAGA[G/T]AATATTATAAACACC | 267 |
| rs558761706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410591 | ACGCAAAAAAAACAT[C/T]ATAATGAGGGCCGGG | 267 |
| rs558792167 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394283 | AAACTGACACCCTGA[C/T]ATCAGAATTAAAAGA | 267 |
| rs558795907 | snp | A/G | 0.000106506 | 0.00729668 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362571 | CTGCATTTGTGGGAC[A/G]TACGCATGAGGCAGG | 267 |
| rs558797391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381694 | GGTTGCTAGAGGCTA[A/G]GGGGAGGAAAGGAAA | 267 |
| rs558857959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381171 | CAGGCAAAGAGAGAG[A/C]GCTTGTGCAGGGAAA | 267 |
| rs558882837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388256 | TTACTATACTGAATG[C/T]TGTAGAGGCAATTAT | 267 |
| rs558917173 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370498 | GGTGCGGATCAAACT[A/G]TTGTACATCTTGTTT | 267 |
| rs558974093 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56408740 | GTGAAAGAAATAAAG[C/G]CTGTGAGAGTGAGAT | 267 |
| rs558977066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56389972 | CCTTACCTCCCTGTT[A/C]CCCTGGCTCACCTCT | 267 |
| rs558978345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400997 | TCTAGCTCCCATATG[A/G]AAAAGAAGAAAATCT | 267 |
| rs558979024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396686 | AAATTGACAAATGGG[A/G]TCTAATTAAACTAAA | 267 |
| rs558989208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367114 | GTCCAGGCACCCTCA[C/T]GGTCCCGAGCCCAGC | 267 |
| rs559113333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56390531 | AATCACTCTGTGTCA[C/T]AAGAGTGTGTGACAG | 267 |
| rs559222297 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426299 | TTCGGCCATAAAAAT[A/G]AACTACTGATACATG | 267 |
| rs559235719 | snp | A/T | 1.64749e-05 | 0.00287005 | missense | AMFR | GRCh38.p7 | 16:56389290 | CTTGATGTTCTTCCC[A/T]GACACGATTATTGTC | 267 |
| rs559339349 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56410231 | AAAGAATGGCAAGGG[C/T]TATCATTTTTACTAC | 267 |
| rs559351382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56383570 | TGTTCCTCCCGAGTC[C/T]TCGCATCTCAGTACG | 267 |
| rs559383621 | snp | A/T | 1.77751e-05 | 0.00298115 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362270 | GGACTGGAGGCTCGG[A/T]AAGTCAGTCCCAGAT | 267 |
| rs559478292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387625 | GACTGTTGAAAATCA[A/G]CAGCAGCTTAATGTG | 267 |
| rs559545560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368296 | GGACCACTTCCCAAA[C/T]TATGTGCATTCAAAT | 267 |
| rs559600164 | in-del | -/GG | 0.473909 | 0.111197 | intron-variant | AMFR | GRCh38.p7 | 16:56406126 | AGGGGAGGGGGGAGA[-/GG]GGAGAGAGGAGAGGA | 267 |
| rs559617555 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56374837 | ATAAATAAAAACTGT[C/T]CTTTAACATAACATT | 267 |
| rs559619109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380591 | ACTGAATGCCTTTAA[C/T]AGCATCCAAGTCACC | 267 |
| rs559721411 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56366271 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 267 |
| rs559763118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381313 | CACGTGGGAACTCAA[C/G]AGGAAATGTGGGTGG | 267 |
| rs559772623 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | AMFR | GRCh38.p7 | 16:56395100 | AATTCTACCAGAGGT[A/G]CAAGGAGGAGCTGGT | 267 |
| rs559797729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409244 | TCCCCAGGAGACAAC[A/G]ATTCTGCATCTCTTG | 267 |
| rs559824081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388372 | TAGGGCACTTACCAG[A/G]AATGAAGCTTGCATG | 267 |
| rs559902515 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56386418 | GCAGCCCAGCCCAGC[A/G]CCCTCACACGCTCAG | 267 |
| rs559950470 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425319 | GCGCTCGAGGAAGAG[C/T]AGCGGCATGGCGGCA | 267 |
| rs559974884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417261 | CAAAAGATACAAAAA[A/T]TAGCCGGGTGGGGTG | 267 |
| rs559978249 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406870 | GTTTGGATAATATTA[C/T]ATTAGTTGAAAGTTA | 267 |
| rs560057903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413991 | TTGCTCTTAGAAAAT[A/G]CAAACTGAAGTATTT | 267 |
| rs560091373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56417611 | CCTCATGTGACGAGT[C/T]GCAGTCAAAATGCAG | 267 |
| rs560094009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379935 | CACACAGTGCAAGCT[C/G]TCAGCAGATCTACCA | 267 |
| rs560126957 | snp | C/T | 1.65795e-05 | 0.00287914 | intron-variant | AMFR | GRCh38.p7 | 16:56407929 | GAAAACAGACAGAAA[C/T]ACAATCTGAGCAAGT | 267 |
| rs560164342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392244 | AAGACCAAAGGTAGA[C/T]AAAACCACAAAGATG | 267 |
| rs560227157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398318 | ATATAAATGTATCAT[A/T]TATATATATATAAAT | 267 |
| rs560237598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56371576 | CACACTCCCAGGCCA[C/T]CTATATGCACCAAGA | 267 |
| rs560327621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413297 | GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCA | 267 |
| rs560370204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400199 | GGAGTACAATGGCAC[A/G]ATCTCAGCTCACTGC | 267 |
| rs560492153 | in-del | -/ACACACACACACAC | 0.0123687 | 0.0776618 | intron-variant | AMFR | GRCh38.p7 | 16:56365544 | GTTGGCATAACATGT[-/ACACACACACACAC]AGACACACGTAGTTG | 267 |
| rs560583733 | snp | C/G/T | 7.13954e-05 | 0.00597433 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362486 | ACAGATGTTACCCCA[C/G/T]GACGTGGGGGCGGGC | 267 |
| rs560585510 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56414949 | ATAAATGTTCTCCAT[C/G/T]CTTGGTGTTGGCTTT | 267 |
| rs560653251 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56406790 | CTAAAATAAAAGTAT[A/C]TACTATAGTATGAGC | 267 |
| rs560661105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56408441 | CTCCTCTCACCTTCA[A/G]CAGGACTCAGGACAG | 267 |
| rs560679438 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56389034 | GGGACCACTGCCATA[C/T]ATATGGTTTGCCATG | 267 |
| rs560907256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56394471 | ACTGCTGGCCGGGCG[C/T]AGTGGCTCACGCCTG | 267 |
| rs560930952 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56411325 | CACTGCAGCCCCAAA[C/G]TCCTGCGCTCAAGCG | 267 |
| rs560970443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401325 | CTGGTGTGCTCTTAA[A/G]GCTTCTTTTGGGCAT | 267 |
| rs561001521 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393416 | AAAAGACACAGACTG[C/G]CAAATTGGATAGTCA | 267 |
| rs561005231 | snp | A/C/T | 6.86719e-05 | 0.00585929 | intron-variant | AMFR | GRCh38.p7 | 16:56386074 | CCTGACTCTTTCCCC[A/C/T]GTCATCTGCTCTCAC | 267 |
| rs561033191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373714 | GCATGCAGGAACAGA[C/T]GGGCAGCATGAGCAG | 267 |
| rs561068059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392880 | GCCACAAAGATACTC[C/T]TCGAGAAGAGCAACT | 267 |
| rs561110178 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | AMFR | GRCh38.p7 | 16:56399093 | TTACTAAAAAAAAAA[A/C]CAAAATTCACCATAA | 267 |
| rs561137733 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56421804 | GCCCAGAAATGAGTA[A/C]CAAAATAAAAACTCA | 267 |
| rs561148483 | snp | C/T | 0.00279162 | 0.0372561 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361338 | CCAACCAAAATAGTA[C/T]ACACAAAATCCAAAT | 267 |
| rs561257922 | snp | A/C | 0.021333 | 0.101051 | intron-variant | AMFR | GRCh38.p7 | 16:56395149 | ATTCCAATCAATAGA[A/C]AAAGAGGGAATCCTC | 267 |
| rs561450761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399816 | GAATTTTGCCTCAAA[G/T]AAATTAAATCCTAAA | 267 |
| rs561454108 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56379999 | ATAGCTCCATTAGGC[A/G]GTGCCCTAGCAGGCA | 267 |
| rs561567394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365362 | GTGTCCTGGAGCTTG[A/G]ATAGGGCTCCTGCAG | 267 |
| rs561595028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380382 | GGCCTGTGATGAGAG[C/G]GGGCTGCTGTGAAGA | 267 |
| rs561660929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384555 | AGGTGGTTTGCACTG[A/G]ATTTCAACAATGGTG | 267 |
| rs561782072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418322 | CAGCCTGACCAACAT[A/G]GTGCAACCCCATCTC | 267 |
| rs561831979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371671 | CATGCTTCCTTCTTC[G/T]TTTATTATGGCCCCA | 267 |
| rs561837444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413342 | GCCCGGCCAACGTGG[C/T]GAAATCCTGTCTCTA | 267 |
| rs561849851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411485 | CTGGGCTCAAGTGAT[C/G]CCACCTTGGTCTCCC | 267 |
| rs561880788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56372279 | CCTCCTGCAGCCATC[A/G]TTCTGCTGTCTGTAA | 267 |
| rs561901999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420891 | AATTTGCATAATTAA[C/G]TCAGAACCTTGACAG | 267 |
| rs561913874 | in-del | -/AAAAAAAAAA | 0.44333 | 0.158505 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361754 | AAGCTTTCAAAGAGT[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 267 |
| rs561959517 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | AMFR | GRCh38.p7 | 16:56396721 | TTCTGCACAGCAAAA[-/G]AAACTACTGTCAGAG | 267 |
| rs561966411 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427463 | ACAGTAGTTCTAAAC[G/T]GTCACAAACCAAATT | 267 |
| rs561983963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412273 | TGGATGACATTAAAC[A/G]TAAATAAACCAACAC | 267 |
| rs562038836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377407 | ATGCAGAAAAATCAC[C/T]CAACAAAATCCAACA | 267 |
| rs562039495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56382650 | GGTACAAAGTTTCGA[C/T]TGTGCAAGATGAAAA | 267 |
| rs562079131 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379799 | TCGCATCTGGGTCAC[A/G]CTGATGCAAGAGACG | 267 |
| rs562104501 | snp | C/T | 0.000428979 | 0.0146392 | missense | AMFR | GRCh38.p7 | 16:56414301 | ATACACTGGATGAGC[C/T]TAGCCACCAACATCA | 267 |
| rs562158857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369427 | GCAGTGAATGTGGCA[C/T]CATGCCCTGAAAACA | 267 |
| rs562192889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367186 | GGCAGGGCTGGCCCC[A/G]GGGAACACAACCCCT | 267 |
| rs562224774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56364161 | AGGCCTCCCTCCTAA[A/G]CAGGTTCCTCACCTA | 267 |
| rs562246134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397448 | AAGACACACACCACA[G/T]GTTCTCACTCATAGG | 267 |
| rs562319576 | in-del | -/TCC | | | intron-variant | AMFR | GRCh38.p7 | 16:56365932 | GTGAAATACATACTT[-/TCC]TCCATTATATATACA | 267 |
| rs562348261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404291 | TTAGAAATGTGCCAC[A/G]TCTAGCCCAATAATT | 267 |
| rs562355943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56363738 | CAGAGGTAGACCAGT[A/G]GGGCCCAGTGTTACC | 267 |
| rs562401814 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426357 | TGCTAAGTCAAAGAA[A/G]ACAGCCACAAAGGTC | 267 |
| rs562438668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421736 | ATCCAAAACCATGCT[A/G]GAATGGACCAAGAGG | 267 |
| rs562463818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385818 | TCCACTCTGCCAGAG[A/C]AGAGTAAGACCAACA | 267 |
| rs562469043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371907 | GTGTATAACAACCAT[C/T]TACTCAGCATTTACA | 267 |
| rs562513764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412312 | AGGGAAGATGCGATC[A/G]ATGCTGAAAAAAATT | 267 |
| rs562516445 | in-del | -/GGCAAGTCCCTCATCTCATCTGAGATAA | 0.00558209 | 0.0525346 | intron-variant | AMFR | GRCh38.p7 | 16:56379573 | TCTCATCTGAGATAA[-/GGCAAGTCCCTCATCTCATCTGAGATAA]GGCAAGTCCCTAACG | 267 |
| rs562573300 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56378797 | GATCTTAATAGATAC[A/T]TCACCAAAGATAGAT | 267 |
| rs562575524 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56413830 | GGCTTCTTTAAAAAC[A/G]ACATTCCTAAAAGTC | 267 |
| rs562599050 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56410378 | AAGTACAAAGAAAAT[G/T]AAAAATGCTGCCTTA | 267 |
| rs562657208 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | AMFR | GRCh38.p7 | 16:56366101 | CAAAAACTGGAGGCC[A/G]GGCGCGGTGGCTCAC | 267 |
| rs562693407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363849 | TTTAAAAAGAGAAGA[C/T]GGCCTGACAACGGCC | 267 |
| rs562774102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419289 | CGGCCTCCCAAAGTG[C/T]TGAGATTACAGGTGT | 267 |
| rs562778704 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56407715 | TTTTTCCTTCAAAAT[G/T]ATGAGTACAGTTTAT | 267 |
| rs562786350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405800 | CAAAACCAGCCTGGG[A/C]AACATGGTGAAACCC | 267 |
| rs562834817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370676 | ACATCTCAGAGTTTA[C/T]GTAGGGCTCTAGGGT | 267 |
| rs563062829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392089 | AGCCTCCACTGCTGA[A/T]ACCCAGGCAAACAGG | 267 |
| rs563074556 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | AMFR | GRCh38.p7 | 16:56363682 | TCTCTCGGCAAGCGT[-/G]GCCAAAGGGGTCCAT | 267 |
| rs563082348 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391654 | TGATTGAACTGCAAG[C/G]TGGCAGCGAGGCTGG | 267 |
| rs563136148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385374 | GTAATCCAAGCACTT[C/T]GGGAGGCCAAGGCGG | 267 |
| rs563147081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398106 | TATAAATGTATCATT[A/T]ATAATATATAAATGT | 267 |
| rs563157777 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56366854 | AGGTGGCACCTCGGC[C/T]CTGCTGCTTGGAGTT | 267 |
| rs563190556 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394822 | GAAGAATCAAACAGA[C/T]GCAGTAAAAAATGAT | 267 |
| rs563194751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391368 | GGACAGTGGGTGCAG[C/T]GCACCGAGCATGAGC | 267 |
| rs563243414 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56407548 | ACCACGCCCAACTAA[-/T]TTTTTTTTTTGTATT | 267 |
| rs563317032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403488 | ACTTATTATACTATA[G/T]AACTACATATTACTA | 267 |
| rs563493628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424523 | CAACGTCTGAATTCT[A/C]CCCTCTGCCCTCTCC | 267 |
| rs563494973 | snp | C/T | 0.000159723 | 0.0089351 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362358 | CTCTGCTCCAGGTAT[C/T]GAACCAAGAGTTCCT | 267 |
| rs563668046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381399 | CATAAAAACCTGCAC[A/G]TAAATGTTTATAGCA | 267 |
| rs563704484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56418150 | CTAGCCTGGGCAATC[A/G]GAGTGAGACTCTGAT | 267 |
| rs563775244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377600 | ACCACTGCTTTCCAA[G/T]GTCATCCTAGAAGTC | 267 |
| rs563803691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381903 | GTTGATAATGGGGAA[A/G]GCTGTGTGTGTGTGG | 267 |
| rs563901413 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56370841 | GAAAAGTTCTAATAA[A/C]TATAACAAAAAAAGG | 267 |
| rs563982685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410788 | TTGGGAGGCTGAGGC[A/C]TTAGAATTGCTTGAA | 267 |
| rs564052616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391584 | GGGTCCCATGCCCAC[A/G]GCTCGGAGGGTCCCA | 267 |
| rs564080236 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56415729 | TGCCCCAAATATCCT[-/A]ATCTGTGTAACAGAC | 267 |
| rs564097409 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56391384 | GCACCGAGCATGAGC[C/T]GAAGCAGGGCAAGGC | 267 |
| rs564106579 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426231 | GATGGGAACAACGCT[A/C]ATGTCCGTCAAGCGA | 267 |
| rs564169819 | snp | C/T | 0.0103295 | 0.0711199 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425617 | GCGGCCTTCGTCCCC[C/T]GCCCCCAGCGGTCGC | 267 |
| rs564216762 | in-del | -/TA | | | intron-variant | AMFR | GRCh38.p7 | 16:56423173 | TCACTTCTACTCAGC[-/TA]TGCTAAAGCAGAAAC | 267 |
| rs564241396 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56419590 | CTGAGGTCAGCAGTT[C/G]AAGACCAGCCTGGCC | 267 |
| rs564322744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56382430 | GGTATCCAATATTTT[A/G]GCTTCCCTGGGCCAC | 267 |
| rs564332513 | snp | A/G | 0.000166898 | 0.0091335 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364049 | CTCCACTTCCACCTC[A/G]CCGAAGTCCAGCGTC | 267 |
| rs564376061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420707 | GAAGTCACTTTCAGC[C/T]CTTAATTTTGTTTTG | 267 |
| rs564436925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56376750 | AATCAAAATGAGAGC[A/G]GACATCAATGAAACT | 267 |
| rs564473980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363218 | CCCCAACAGATGGGC[A/G]CAAATTCTCTCTGCA | 267 |
| rs564494839 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398788 | ATGCCTATAGAACCA[C/G]AAAAATAGCAAACTA | 267 |
| rs564518301 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409196 | TGACCCCATGTTAGC[A/C]GTAAGTAAACACTAT | 267 |
| rs564611407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418275 | CTTTGGGAGGCTGAC[A/G]AGGGAGAATCACGAC | 267 |
| rs564712918 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | AMFR | GRCh38.p7 | 16:56376984 | AGTTGTATAGATAAT[A/T]AATAATCTTCCACAG | 267 |
| rs564723711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397378 | TTCATGTCCTTTGTA[A/G]GGACATGGATGAAGC | 267 |
| rs564744796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410851 | CATGCCACTGCACTC[C/T]AGCCTGGGCAACAGA | 267 |
| rs564780563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395312 | CAAATGCAGCAGCAC[A/G]TCAAAAACCTTATCC | 267 |
| rs564785195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56396964 | ATCAGAGAAATGCCA[A/G]TCAAAACCACAATGA | 267 |
| rs564791885 | snp | A/G | 3.53245e-05 | 0.0042025 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362818 | AATGCAGTCAAGCCC[A/G]CTTTTCCATGGAGCG | 267 |
| rs564855007 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417368 | GGAACCGTGATTGCA[C/T]CACTGTACTGCTCCA | 267 |
| rs564880916 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56389775 | TCCACTCTGACGCTC[A/G]TGTCTTTCACTCTGC | 267 |
| rs564918485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | AMFR | GRCh38.p7 | 16:56388786 | ATCAGTATCACTGTC[A/G]ACCACCTCCACCTCC | 267 |
| rs565101138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56373755 | ATCTTAAGAAAGAAC[C/T]AAAGAGAAGTGCCAG | 267 |
| rs565119102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56393503 | GGCTCAAAATAAAGG[A/G]ATGGAGGAAGATCTA | 267 |
| rs565136081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380434 | ATTTTCCCCATTGTC[C/T]TGGGGATTAACATTC | 267 |
| rs565164778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374704 | CAAAGTTGGAATATG[C/T]TGCCGTGAGACCTAC | 267 |
| rs565208498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56389771 | GTCCTCCACTCTGAC[C/G]CTCATGTCTTTCACT | 267 |
| rs565225027 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391819 | CAAAAGGCAGCAGAA[A/T]CCTCTGCAGACTTAA | 267 |
| rs565315130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395378 | TGCTGGTTCAACATA[C/T]GCAAATCAATAAATG | 267 |
| rs565317119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388024 | TCTCTATCCATCCAT[C/T]CATCCATCCCACCTA | 267 |
| rs565378501 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | AMFR | GRCh38.p7 | 16:56394668 | GAATGGCGTGAACCC[A/G]GGAAGCGGAGCTTGC | 267 |
| rs565402980 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56394150 | GAAATAAAGATGTTC[C/T]TTGAAACCAACGAGA | 267 |
| rs565420115 | in-del | -/AG | 0.00159617 | 0.0282053 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426536 | TCTGTGGCCCAGGCT[-/AG]AGAGTACAGTGGCAT | 267 |
| rs565455294 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56388944 | GTATGTAAGTATGAG[G/T]ACACTTTAAAATAAT | 267 |
| rs565500246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417391 | CTGCTCCAGCCTGAG[C/G]AACATAGTGAGGCCT | 267 |
| rs565520599 | in-del | -/GCTTTCCAG | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56386383 | CTGCTGAGCAATCCT[-/GCTTTCCAG]GGGGGCTGGATGCAG | 267 |
| rs565561775 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424930 | CTCCCTCAGCAGCGC[A/T]CCCGCGAGCAAGGCC | 267 |
| rs565577843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424356 | AACATCAGGTAAAGG[C/G]AGCAGAAAAGGAAGC | 267 |
| rs565581342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56402097 | AATCCCAGCACTTTC[A/G]GAGGCCGAGGTAGGG | 267 |
| rs565635156 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417914 | ATGTCTATAATCCCA[C/G]TACTTTGGAAGGCCA | 267 |
| rs565653896 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423184 | TCAGCTGCTAAAGCA[G/T]AAACTACATATACAC | 267 |
| rs565729330 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56389937 | TCTGCTTTCTCCTCA[A/G]GCATGACAGCCGTAC | 267 |
| rs565758561 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56419292 | CCTCCCAAAGTGCTG[A/C]GATTACAGGTGTGAG | 267 |
| rs565770296 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56366440 | TTAGAAGCCATGCAC[C/T]ATTTCACAAATGATG | 267 |
| rs565916627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368699 | GACAGATGGCACAGC[C/T]CCTAGAGCAGGGGGT | 267 |
| rs565956940 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370114 | CGCAATACCTGCATG[G/T]AAGAAACCTGCACTT | 267 |
| rs565993814 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367248 | GGAATGACTGCCAGC[C/T]CTGCGTGGAAACACA | 267 |
| rs566056147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380059 | GCCTTCCGCACTGCC[A/G]TAGCAGAGGTTCTCC | 267 |
| rs566130629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403835 | CAATTTATGAATGTA[C/T]GTACTCAAATACATA | 267 |
| rs566167166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423821 | CCTTCTACTAAACTC[C/T]CCATCAGAAGGACCA | 267 |
| rs566229731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408583 | TACCACTACTACAAC[A/G]TGATGTCAGCATTAT | 267 |
| rs566303648 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56416097 | CAGCTTTATTACGAC[A/G/T]CAATTTCTTAAAATA | 267 |
| rs566308671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56406481 | AAATGAGAGGATCAC[C/T]TGAGCCCACAAGGTG | 267 |
| rs566438240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365609 | ACACACACGCACACA[C/T]ACGCTGGAGTCTCAC | 267 |
| rs566563879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407254 | GATATTAGCCAATTA[A/G]CTTCAGTTTATCTAA | 267 |
| rs566631866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377860 | CAGTATGCTTTATAT[C/T]AGCGCCCACAAAACA | 267 |
| rs566669318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386274 | GTCTTTGGTCTCTGA[C/G]GCACTTAGAAGTTAG | 267 |
| rs566713414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387014 | AGGCAGGAGAATCAC[C/T]TGAACCAGGGAATCA | 267 |
| rs566713762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56392549 | TGAAAACCATGGCAC[A/G]AGAACTACGTGACGA | 267 |
| rs566804847 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56384953 | ATTACAGGTGCATGC[C/T]AACATGCCCAGCAAA | 267 |
| rs566811524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421215 | CCTGCCTCAGCCTCC[A/G]CCTCTCAAACTGCTG | 267 |
| rs566837082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391496 | ATCAGGTCACTCCCA[A/C]CCTAATACTGTGCTT | 267 |
| rs566865655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391735 | GGGAAGCTCGAACTG[A/G]GTGGAGCCCACCGCA | 267 |
| rs566954166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407294 | TTTTAATTAATAATA[C/T]TAATTATGGGTAAGA | 267 |
| rs566979340 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56412291 | AATAAACCAACACAG[A/C]ACAGCAGGGAAGATG | 267 |
| rs567044293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371195 | CTTTATTCTTAAACA[A/G]CTTCCTCCTCATTTC | 267 |
| rs567090416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56364393 | ACCAGCATGAAAAAC[C/G]TAAGCACCTTCAAGC | 267 |
| rs567105114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56371995 | CAGGTTATATACAAA[C/T]AGTATCCTTCCCCCA | 267 |
| rs567181717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378364 | ACAATAGAGAAAAGA[C/T]AGACTTTTCAACAAA | 267 |
| rs567305971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392401 | GAAGAAGGCTTCAGA[A/C]AATCAAACTTCTCCA | 267 |
| rs567369762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391847 | TAAATGTCCCTGTCC[A/G]ACAGCTTTGAAGAGA | 267 |
| rs567377415 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56393236 | ATGGAAAAGAACAAC[C/T]GGTACCAGCCACTGC | 267 |
| rs567437823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56382694 | GGACAGTGGTGATAG[C/T]TGCACAATGTGAATA | 267 |
| rs567439592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385432 | ACCAGACTGGCCAAC[A/G]TGGTGAAACCTCGTC | 267 |
| rs567451255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56387060 | TGAGATCACGCCACC[A/G]CACTCCAGCCTGGCA | 267 |
| rs567477892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56413545 | AATTATTCTACACCC[C/T]ACCCACTCAAATCCT | 267 |
| rs567506839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386726 | CACCAAGAATTGGCT[A/G]TAAAACAACCCAATT | 267 |
| rs567541103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421279 | TAAGTTTTATAATAA[C/T]ACGAAAATCGGCTCT | 267 |
| rs567587443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380189 | ACTTCTGTGCACTCG[C/T]AGGCTCAACACCACC | 267 |
| rs567587503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387828 | TCTCAATGATCCTTC[A/G]TTATATGCTTAAATG | 267 |
| rs567612069 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56378994 | ACTGCTGGTGAGAAC[A/G]CAAGATGATACAGCC | 267 |
| rs567646651 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56412718 | CTAAACAATTAGCCA[A/G]GTGTGACACATGCCT | 267 |
| rs567688772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370325 | CAAAAGCCAGGCATA[G/T]GATTCCATTTATATG | 267 |
| rs567698293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398398 | ATATTGGAGAAGTGA[A/G]TATTTTGAAGGGATA | 267 |
| rs567749680 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56370950 | TAGAAGGAGCAGGGA[C/G]TATGTCAACGTCAGG | 267 |
| rs567751569 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56363464 | ACGCACAGATGCGCT[C/G]AGTGTGTGTACAATG | 267 |
| rs567794106 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390496 | GGAGTTTCCTAGAGG[C/T]CAAGATGGAGCTACT | 267 |
| rs567815954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372690 | TGCTTTCGAATCTAC[A/C]CTTAAAAAACAACAG | 267 |
| rs567827084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56365216 | CCGAGAGTCAAAGGA[C/T]GGGGGAACTGGTGGC | 267 |
| rs567840644 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56392595 | TAGCCAATTCCATCA[A/C]CTGGAAGAAAGGGTA | 267 |
| rs567850056 | in-del | -/ATAAT | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56412031 | TTGGGGGAATTATAC[-/ATAAT]ATATGTGAAATGGTT | 267 |
| rs567975913 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56399082 | CTTAAGAATTATTAC[-/T]AAAAAAAAAAACAAA | 267 |
| rs568132373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405139 | TTATATATTTCATAC[C/G]TGCTACATCTTAAAA | 267 |
| rs568152160 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399575 | TATATGATTCCTTTA[C/T]ATGAAATGTCCAGAA | 267 |
| rs568161896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411927 | TTAGTTTCTGTGTGA[C/G]CTTGGGAAAGTCACT | 267 |
| rs568238967 | in-del | -/AC | 0.485759 | 0.0831739 | intron-variant | AMFR | GRCh38.p7 | 16:56365557 | TACACACACACACAC[-/AC]AGACACACGTAGTTG | 267 |
| rs568253175 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374651 | CACAAAATTATCCTT[C/T]CAAAAGGATGCAGAA | 267 |
| rs568267454 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425849 | TCGGCCACTTGCCCC[C/G]CCCCCACCCCATTAA | 267 |
| rs568277175 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56404561 | CAGGAATTCCCATTA[A/C]CACCTACAAAGTACC | 267 |
| rs568298374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412523 | CTGACCAATTTCTGG[G/T]CCACAAATAAAAAAT | 267 |
| rs568336018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410903 | AAAAAAAAATTGTGA[C/T]GAATATTTTTGTATG | 267 |
| rs568413025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403146 | GAGAATAAAACACAC[A/G]GTAAAAGCGAACGTG | 267 |
| rs568617027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384007 | GGCTCTGAAATCTCA[A/G]TTCCTATCACAGTGT | 267 |
| rs568716035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397029 | TAAAAAGGAAACAAC[A/G]GGTGCTGGAGAGGAT | 267 |
| rs568720472 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426912 | TAAGCTGTTACCAAA[A/G]GAAAAAAATGTTACC | 267 |
| rs568723458 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | AMFR | GRCh38.p7 | 16:56364224 | AAAGAGAAGGCTGCT[A/G]CCAAGCAGGGAGGCA | 267 |
| rs568731062 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403484 | TTTCACTTATTATAC[C/T]ATATAACTACATATT | 267 |
| rs568790112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419704 | GTGGCTGAGGCAGGA[C/G]AATTGCTTGAACCCA | 267 |
| rs568837517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56412591 | TAAGCCAGTAGAAGT[A/G]GCTCACACCTATAAT | 267 |
| rs568861433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370989 | GGAAAAGGTCGGCAC[C/T]GGGCTCTGCTTAGAG | 267 |
| rs568937613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413392 | CTGTGGTGCACACCT[A/G]TATTCCCAGCTACTT | 267 |
| rs568945508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403706 | TACAGCTATCTGATG[A/G]TATTTTTATCCTGAA | 267 |
| rs569052702 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56391352 | CTCACTGGGGCTTGT[C/T]GGACAGTGGGTGCAG | 267 |
| rs569053998 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378578 | CAAAGGCACAATCCA[C/T]GAAAGAAAATAATTG | 267 |
| rs569068730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56392444 | AAGTTTGAACCCATC[A/G]CAAAGAAGTTAAAAA | 267 |
| rs569206023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56397137 | TTCCTCAGGGATCTA[C/G]AACTAGAAATACCAT | 267 |
| rs569250203 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56422809 | TTGTTCACAGATATG[C/T]CCTCCAAAGTGCCCA | 267 |
| rs569280705 | snp | A/C | 0.00387424 | 0.0438419 | intron-variant | AMFR | GRCh38.p7 | 16:56386047 | ACAAGAATCCAGTGT[A/C]AGTTTCAGAGCCCTG | 267 |
| rs569295244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381662 | GGCAAAGCTATGAAG[A/G]TAGTAAAAAGATCAG | 267 |
| rs569295411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390041 | CCTCTTCTCTTTGCA[C/T]GCTGTTTTCCCAACA | 267 |
| rs569359778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56389130 | TAACTAAAATAGTAT[C/T]TGCTTAAGGGAGAAC | 267 |
| rs569397450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391475 | GTGACAGACTGCACC[G/T]GGAAAATCAGGTCAC | 267 |
| rs569459693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384048 | CTTGCCAGGCCCCAA[C/T]CATAATGACCTTTCT | 267 |
| rs569525140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419063 | GAGTCTCACTCTGTC[A/G]CCCGGGCTGGACTGC | 267 |
| rs569563918 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407664 | TAAAAGAGTGAAAAA[-/T]TTTTTAAATCTTAAA | 267 |
| rs569593991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384670 | GCCAACAGCACGCCT[C/T]AACATTTCAAGGCAT | 267 |
| rs569599419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396103 | GTGAAAATGGCCATA[C/T]TGCCCAAGGTAATTT | 267 |
| rs569610986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411064 | ATTTGCTTCACTGTA[C/G]TCTTTTACACAGAGG | 267 |
| rs569674089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56376007 | AGGTTGCAGTGAGCC[A/G]AGATCGGGCCACTGC | 267 |
| rs569719225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369559 | TCAACATAAGGAGAG[C/T]TCAGAAAACCAACTG | 267 |
| rs569771188 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426424 | CAATAGGCAAGTACA[C/T]ATACAGACACAGAAA | 267 |
| rs569835292 | snp | A/G | 3.55164e-05 | 0.0042139 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362543 | TTCCCACTGGGTGTG[A/G]TGCTCAGGACACCTG | 267 |
| rs569853342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417981 | CAGACTGAGCAACAT[A/G]GCAAAACCCCATCTC | 267 |
| rs570051501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423902 | TGAAGCACAGTGGGA[C/T]TAATTATAACAAATG | 267 |
| rs570138630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374109 | AGGAGGTGGAGGTTG[A/C]AGTGAGCCGAGATCG | 267 |
| rs570150877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369692 | AAAGAAATCATTATA[C/T]ATGAAAGATACCTGC | 267 |
| rs570157855 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56417187 | GGCCAAGGTGGGGGG[A/T]TTGCTTGAACTCAGG | 267 |
| rs570210202 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56373270 | ACAACGTCTGCCCTC[A/G]GGAGAAACTACTCAA | 267 |
| rs570222959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56376034 | CTGCACTCCAGCTTG[C/T]GCAACCAAGTGAGGC | 267 |
| rs570295632 | snp | C/T | 1.66524e-05 | 0.00288547 | missense | AMFR | GRCh38.p7 | 16:56409554 | ATGAAAATGAACTTG[C/T]AGAAAATAAAATTCC | 267 |
| rs570339446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56395482 | CAAAATTCAACAGCC[C/T]TTCATTCTAAAAACT | 267 |
| rs570419625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56404506 | CTTTTTTTAATTACA[A/G]AGATGGAAAATGTAT | 267 |
| rs570475365 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425852 | GCCACTTGCCCCCCC[C/T]CCACCCCATTAACCC | 267 |
| rs570514408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363427 | CACACCTGCTGTAGC[C/T]GCCACCAACCATGGG | 267 |
| rs570515544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56418455 | GTTGCAGTGAGCCGA[A/G]ATCATGCCACTGCAC | 267 |
| rs570517543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411815 | AGGAATCGTTGGTGA[A/C]ATGTCTGTTTCCAGA | 267 |
| rs570652844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411108 | ACAATCTTCACTAAC[A/C]CTGAAATAGGAGAGC | 267 |
| rs570784566 | snp | A/C | 1.78433e-05 | 0.00298686 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362433 | TCTGGCCTCTGGCAC[A/C]GTCTACATGCTTCCA | 267 |
| rs570789631 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361856 | CCTTAAAGTTAAACA[C/T]GTGAAGAATTTGAAG | 267 |
| rs570793559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409842 | GAATGTTAGCTATTC[A/G]AAGGATAGCGATATT | 267 |
| rs570949620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400746 | TGGATTTTTTCATTA[C/T]AAGCTCTCAAGAACC | 267 |
| rs571032730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56396124 | AAGGTAATTTATAGA[C/T]TCAGTGCCATCCCCA | 267 |
| rs571062282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56424010 | ATGCAAGGAGACAAG[A/C]TCCAAGAAGCCATAT | 267 |
| rs571062371 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390128 | ACATTCAATAAATAC[C/T]TGAGGTGTCCATTAA | 267 |
| rs571139379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390160 | GAAAGGAAAGGGTAC[C/T]AGAGTAAGAAGCAGA | 267 |
| rs571200248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424639 | CGGGATAACGCACTC[A/C]CAGATCCCGACCTCC | 267 |
| rs571267690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56387129 | AAGTGGAATGGCTAT[C/T]TCAAAGGTCTTGAGA | 267 |
| rs571323380 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411686 | AGTGGAAAAAAATCA[C/T]AGAGTATGCCCTAAT | 267 |
| rs571334581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56394496 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 267 |
| rs571388076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367185 | TGGCAGGGCTGGCCC[C/T]GGGGAACACAACCCC | 267 |
| rs571431048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56379723 | GGCCACATGCAAGTC[C/T]AAAATAAGGTAGGGC | 267 |
| rs571475716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407443 | CTGGAGTGCAGTGGC[A/G]CAATGTCTGCTCACT | 267 |
| rs571504636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56375100 | TAAAACAAGCTTGTC[C/T]GACTCATGGCCCACA | 267 |
| rs571568289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393100 | CAAGCCAGAATTTCA[C/T]ATCCAGCCAAACTAA | 267 |
| rs571591034 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56381484 | GAACGAATTAACAAA[C/T]TGTGGTATATCCAGA | 267 |
| rs571603448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56386218 | CCTCCTATTATCATT[C/T]TTATAGTATCCTTCT | 267 |
| rs571612120 | snp | A/G | 8.28e-05 | 0.00643375 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408024 | GGTGATGGAGCAGAC[A/G]GCCGCCAGTCCACAG | 267 |
| rs571778628 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | AMFR | GRCh38.p7 | 16:56366332 | GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC | 267 |
| rs571778753 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56415011 | TGGAATGGGTTAAAC[A/C]GAAGGAAAAGAAAAC | 267 |
| rs571779271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414454 | CAGTGACTGAGCCTT[C/T]CTGGTTCTCTCCCAA | 267 |
| rs571790960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366964 | CCACTCAGCTCAGGC[A/G]GTCTCAGTTTTGCAA | 267 |
| rs571794696 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56415691 | AATCCTTCAAACAAC[C/T]AGGAACAAACGCCCA | 267 |
| rs571841633 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56423162 | CTTTTGAGATTGTCA[A/C]TTCTACTCAGCTGCT | 267 |
| rs571988717 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56380307 | CAAGTACCTAGGCTG[A/C]ACACAGCACAGGGAC | 267 |
| rs571991380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374376 | GATCCAGGAATCTTA[C/G]AGAGTACCAAGCAGG | 267 |
| rs572050074 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56387260 | AGTAGTCATAATTCA[A/C]AAAATAATGGATTAC | 267 |
| rs572064946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56380899 | CTGTCTTCTCCTGAG[C/T]CCTCCAAACTGTCCC | 267 |
| rs572116951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56366831 | GGGCACGGGCAGGGG[A/G]TGGGGGGAGGTGGCA | 267 |
| rs572172673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408410 | TAGAAGCAATGTTCC[A/G]AGGGTATACAACTCT | 267 |
| rs572210290 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388931 | GTAAATTTTTTTTGT[A/G]TGTAAGTATGAGTAC | 267 |
| rs572250304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409905 | AGGCGCAGTGGCTCA[C/T]ATCTGTAACCCCAGC | 267 |
| rs572276171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56393331 | ATAACCAGCTAACGT[C/T]ATAATGACAGGATCA | 267 |
| rs572299987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401918 | CCACTTGATAGACTG[C/T]GCCTGTATCACAACA | 267 |
| rs572304892 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362027 | TAAAGCCCTTCAAGG[C/T]TTACTCTCCCATCTT | 267 |
| rs572309964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56406809 | TATAGTATGAGCTGA[C/T]GGGCCTAAGTTAAAT | 267 |
| rs572377316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367206 | ACACAACCCCTTTCT[A/C]TTCCAGCACATGAGG | 267 |
| rs572523120 | in-del | -/CC/CG | 0.104504 | 0.2033 | intron-variant | AMFR | GRCh38.p7 | 16:56365601 | TACATACACACACAC[-/CC/CG]GCACACACACGCTGG | 267 |
| rs572531517 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56376237 | CAGAAAATCAGTTAA[G/T]AACATAGCTGAACTC | 267 |
| rs572822979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405500 | AATCCCCCTACAATC[C/T]TGAGGTTTACCCTGG | 267 |
| rs572844252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391589 | CCATGCCCACGGCTC[A/G]GAGGGTCCCATGCCC | 267 |
| rs572905461 | snp | A/C | 0.486 | 0.0824865 | intron-variant | AMFR | GRCh38.p7 | 16:56398052 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
| rs572974036 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56385606 | AAGGAAGACCCTGCC[A/T]CCAGAAAAAAAAATT | 267 |
| rs572987161 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56418665 | ATACAAAAAATTATC[C/G]GGGCACATGGTGGGC | 267 |
| rs573050042 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427307 | AAATGCTAAACTTTA[A/C]ACTTTATCAGTAAAA | 267 |
| rs573073920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378624 | TTAAATGTAAAAAGT[A/T]CTGCAAAAGACAATG | 267 |
| rs573125085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56419090 | CTGCAGCGGCGCATT[C/T]TTGGCTCACTGCAAC | 267 |
| rs573134969 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56383556 | CCCATCCTCATGCCT[A/G]TTCCTCCCGAGTCTT | 267 |
| rs573161315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56421455 | CCTAGTCAAATAGGT[C/T]ACGAGTTTGCCAATC | 267 |
| rs573222291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56420826 | GTTCAAGCAATCCTC[C/T]TGCCTCAGCCTCCCA | 267 |
| rs573258944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56377379 | AAGAAAAGTAACATG[A/G]CCGTATCAGTAGATG | 267 |
| rs573316947 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56412184 | ACTCTATTTCTAGAA[C/T]TTTAAGCACCCAAGA | 267 |
| rs573317894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56393778 | GACTTTAACACCCCA[C/T]TGTCAACATTAGACA | 267 |
| rs573320459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56369925 | AAACTCAAATACCGT[A/G]TGTTCTTATAAGTGG | 267 |
| rs573356734 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56400132 | TTCTACCACCAGAGT[-/C]CAAGCTACTTTTTTG | 267 |
| rs573370390 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378905 | CCACTACATATATAT[C/T]AGAATAGCCAAAATC | 267 |
| rs573375786 | snp | C/T | 0.000106942 | 0.00731162 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362497 | CCCACGACGTGGGGG[C/T]GGGCTCACACTGTGC | 267 |
| rs573459644 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56405322 | AAATGATAAAAGACA[A/C]ACATTTCTCAGTTCA | 267 |
| rs573493797 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | AMFR | GRCh38.p7 | 16:56395295 | TAAAATACTGGCAAA[-/T]CCAAATGCAGCAGCA | 267 |
| rs573541434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56365992 | CATGCTAACTCTAGA[A/G]GCAGCAGTGGAAAAT | 267 |
| rs573588098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56370484 | GTGGAGTTCTGGAGG[A/G]TGCGGATCAAACTGT | 267 |
| rs573618873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398780 | CTAACTTTATGCCTA[C/T]AGAACCAGAAAAATA | 267 |
| rs573653958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56392580 | ATGCACAAGCTTCAG[C/T]AGCCAATTCCATCAA | 267 |
| rs573743149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56384197 | AGAACATCTCCAAAT[A/G]CCTCCTCTAAAATGT | 267 |
| rs573758078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56372894 | GGGAGGCTAAGGCAG[A/G]GCAATTGCTTGAACC | 267 |
| rs573779484 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412307 | ACAGCAGGGAAGATG[A/C/T]GATCGATGCTGAAAA | 267 |
| rs573842796 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | AMFR | GRCh38.p7 | 16:56419180 | AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT | 267 |
| rs573854713 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375389 | AGAGAAAGAGTGGAA[A/G]ACAAAAATAGGAACA | 267 |
| rs573870561 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378972 | GGAGTAACAGGAACT[C/G/T]TCATTCACTGCTGGT | 267 |
| rs573915010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412924 | AGAGTCGATACTGGA[G/T]AAAGTGCTGAAAATG | 267 |
| rs573928535 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386530 | ATGACTACTCACTTG[C/G]AGGCATTTTCACATT | 267 |
| rs573930025 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56370585 | TATTTCAATTATATC[A/T]CAATTTAAAAAAATT | 267 |
| rs573957799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56378500 | GCAAAACTATAATAC[C/T]CCTAGAAGATAACAG | 267 |
| rs573966838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56414592 | CCCAATACGCACCCT[C/T]CAGCAGGCCACCTTA | 267 |
| rs574037641 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | AMFR | GRCh38.p7 | 16:56410291 | AAGATTAGACTTTGT[-/A]AAAAAAAATTCTTCA | 267 |
| rs574109837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405754 | GCACTTTGGGAGACC[A/G]AGGCAGGAGGATTGC | 267 |
| rs574125920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56363749 | CAGTGGGGCCCAGTG[C/T]TACCAGATGCTCTGG | 267 |
| rs574153468 | in-del | -/GA | 0.00121778 | 0.0246456 | intron-variant | AMFR | GRCh38.p7 | 16:56385408 | GATCACTAAGGCCAG[-/GA]GTTCGAGACCAGACT | 267 |
| rs574163622 | in-del | -/ATC | 0.0107246 | 0.0724382 | intron-variant | AMFR | GRCh38.p7 | 16:56366156 | GGCAGAGGCGGGCGG[-/ATC]ATGAGGTCAGGAGAT | 267 |
| rs574207922 | in-del | -/AAAC | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56378750 | AGCTTAACAATAAAA[-/AAAC]AAACAACCTGATCAA | 267 |
| rs574249847 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56411332 | GCCCCAAACTCCTGC[A/G]CTCAAGCGATCCTCC | 267 |
| rs574263401 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56391339 | GTACCAGGTTCATCT[A/C]ACTGGGGCTTGTCGG | 267 |
| rs574269950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56406625 | GTAGAATAAAACTAT[C/T]ACATTATTTATGTTT | 267 |
| rs574304142 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | AMFR | GRCh38.p7 | 16:56369913 | ACTCAGGAACAGAAA[C/T]TCAAATACCGTATGT | 267 |
| rs574337295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403372 | AAAAAGATGTCTATC[C/T]ATGCAATTATAAAAC | 267 |
| rs574415354 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423234 | TGAGCACATGGAGGG[C/T]CTGAGAAACCAAAGC | 267 |
| rs574429475 | in-del | -/ATATTT | | | intron-variant | AMFR | GRCh38.p7 | 16:56420271 | ACATGGTCAATCTGG[-/ATATTT]CTTAGACTCCTGCCT | 267 |
| rs574442985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403963 | GAGGAAAAAAAATTT[A/T]AAAAAAGAAGATAAA | 267 |
| rs574446980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56411178 | TATCAAGCCGTCTAG[C/G]GGGGTCAGGGAGAAC | 267 |
| rs574473551 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56396697 | TGGGATCTAATTAAA[C/G]TAAAGAGCTTCTGCA | 267 |
| rs574509371 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56418482 | GCACTCCAGCCTAGG[C/T]GACAGAGTGAGACTC | 267 |
| rs574544671 | snp | C/T | 0 | 0 | intron-variant | AMFR | GRCh38.p7 | 16:56397730 | TATATAAATGTATCA[C/T]TTATAATATATAAAT | 267 |
| rs574578096 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56397228 | AAGACACATGCACAC[A/G]TTATGTTTATTGTGG | 267 |
| rs574602013 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415629 | ACATTTTTAAAGGAT[C/T]GAAACGAAAATAGTT | 267 |
| rs574672640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56368328 | CTTGTCCCAGGGTCC[A/G]CTTCTGGGGAAATCC | 267 |
| rs574680305 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56396826 | TACAAAGAACTCAAA[A/C]TAATTTACAAGAAAA | 267 |
| rs574718516 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56371582 | CCCAGGCCACCTATA[A/T]GCACCAAGATGTCAC | 267 |
| rs574773342 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402414 | AATCAGAGGAGTAAG[A/G/T]CCCCCAGAGATCCAA | 267 |
| rs574857047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395625 | AAACGGGCACAAGAC[A/G]GGGATGCTCTCTCTC | 267 |
| rs574916624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56376312 | ACTTCATCCAACAAC[A/G]GCAGAATACACATTC | 267 |
| rs574918441 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | AMFR | GRCh38.p7 | 16:56395143 | GAAACTATTCCAATC[A/G]ATAGAAAAAGAGGGA | 267 |
| rs574993388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56389456 | ATTCACCCAGAAGTA[C/T]TCTGGATATATCAAA | 267 |
| rs575075847 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425934 | CCCGAAACCCCAGAA[C/G]AAAGAATATTAACAG | 267 |
| rs575095476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375587 | ATAAAGACACATACA[C/G]ATTAAAAGAAAATGG | 267 |
| rs575140640 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56397341 | TACCATGGAATACCA[C/T]GCAGTCATAAAAAAT | 267 |
| rs575221909 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397366 | AAAAATGATGAGTTC[A/C]TGTCCTTTGTAGGGA | 267 |
| rs575256022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56417612 | CTCATGTGACGAGTC[A/G]CAGTCAAAATGCAGA | 267 |
| rs575338026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56404191 | GGCATGAGCCACCGC[A/G]TCCAGCCGAGGCTCT | 267 |
| rs575341774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56412088 | TAAGCACTTAAAAAC[A/G]CATCAAAAAGCTTCC | 267 |
| rs575386971 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | AMFR | GRCh38.p7 | 16:56391566 | TCCTGCGTGTGGCTC[A/G]GAGGGTCCCATGCCC | 267 |
| rs575681137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56381137 | AGGAGGAGCAAGCCA[C/T]ATCTTACATGGATGG | 267 |
| rs575724642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409147 | GTATCAAGGTTTCCT[G/T]GCACTGTGAACAAAA | 267 |
| rs575798683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56402620 | TTTCAGGAAATGAAC[A/G]GGGTAGAAGCCCAAT | 267 |
| rs575812617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56418186 | AAAAAAAAAAAAAAC[C/T]GCTTAAAAAAAGTAA | 267 |
| rs575820013 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56382402 | GTTAATTGTTTAATG[C/G]GTATAGAGCAAGGGT | 267 |
| rs575860386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56409977 | GTTTGAGATGAGCCT[C/T]GGTAACATGGGGAAA | 267 |
| rs575925688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56375350 | TGGAATTCTATAAAA[C/T]GTTCAGTTAAAACCA | 267 |
| rs575969217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367270 | GGAAACACAGGCCAC[A/G]CCACGGGCACAGCCT | 267 |
| rs575994893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56367982 | AGCCAGTAAGGTCTC[A/G]CCACCTCAGTGCTGG | 267 |
| rs576006848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424248 | TGTGTTAGAATAGAT[C/G]CTCAAATAAGAAACA | 267 |
| rs576021637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56377092 | AATCTCTTTCAGAGG[A/G]CAGAAGCAGAAGGGA | 267 |
| rs576102682 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56374555 | ATCGACAGCTCCTCA[G/T]AAGCCCCACAAGCAA | 267 |
| rs576132799 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56366642 | AGCACCACCCTAGAC[C/G]CAAGCCTGTGTGCAG | 267 |
| rs576144338 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361343 | CAAAATAGTATACAC[A/G]AAATCCAAATCAAAA | 267 |
| rs576180243 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394066 | AAACTCACTCAAAAC[C/T]GCTCAACTACATGGA | 267 |
| rs576189956 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391600 | GCTCGGAGGGTCCCA[C/T]GCCCACGGAGCCTCG | 267 |
| rs576203781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56387411 | GCCAAGTAGCCCCAC[C/T]TACTCTTCTGGGAGA | 267 |
| rs576287988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56395876 | TCACAAACATTCTTA[C/T]ACACCAATAACAGAC | 267 |
| rs576345039 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387474 | GGGATTTCACCAACA[C/T]GACACCATCCCCACT | 267 |
| rs576376953 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367764 | GTCCCACTTTAGTTT[C/T]CTTTTGAATAACAGT | 267 |
| rs576377074 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416860 | ACTTCCTATTTTAAT[C/T]TAAATGAAGATTTGA | 267 |
| rs576437912 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56365615 | ACGCACACACACGCT[A/G]GAGTCTCACTGTCCT | 267 |
| rs576479204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56400977 | ATGTGTTGAGTTACC[A/G]AGACTCTAGCTCCCA | 267 |
| rs576526518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56407605 | TTGGCCAGGCTGGAG[A/T]ATTTTTATTTCTACT | 267 |
| rs576535205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56394769 | AAAAAAAAAAAAATT[G/T]ATAGACTGCTAGCAA | 267 |
| rs576610039 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | AMFR | GRCh38.p7 | 16:56393989 | gcaaatgtaaaagaa[C/G]agaaatcataacaaa | 267 |
| rs576656812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56403281 | ACTCTAAACAATGCA[C/T]ATCCTCGTCAGCCTA | 267 |
| rs576720750 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56411014 | TTCCAAAGCAGTCCT[A/G]TAAGTGTACATTCCC | 267 |
| rs576725548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56410138 | ATCATCATGCCACTG[C/G]ACTCCAGCCTGGGTG | 267 |
| rs576732546 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56397184 | ATTACTGGGTATATA[A/C]CCAAAGGAATATAAA | 267 |
| rs576854995 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | AMFR | GRCh38.p7 | 16:56410623 | GTGGTGGCTCATGCA[C/T]GAAATCCCAGCATTT | 267 |
| rs576955459 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56367949 | ATCTCACACAATGCT[A/G]CAGACACTCTGGGGA | 267 |
| rs577000877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56381217 | CATCAGATCTTGTGA[A/G]ACTTATTCACTATCA | 267 |
| rs577008680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56374708 | GTTGGAATATGTTGC[C/T]GTGAGACCTACCTTA | 267 |
| rs577070562 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | AMFR | GRCh38.p7 | 16:56375469 | TCCAAATACATTAAT[A/T]ATCACTTTGAACATC | 267 |
| rs577071528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56390487 | TAAGTAACAGGAGTT[G/T]CCTAGAGGCCAAGAT | 267 |
| rs577131251 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | AMFR | GRCh38.p7 | 16:56394210 | GACACATTTAAGGCA[C/G]TGTGTAGAGGGAAAT | 267 |
| rs577147159 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56396334 | TGGTACCAAAACAGA[G/T]ATATAGACCAATGGA | 267 |
| rs577211604 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419898 | CTCACCAAATGCCTT[A/T]TTTTTCCAGTCTACA | 267 |
| rs577340852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56401044 | TAAAGAAAGGAAGAT[C/T]AAAGATGCAAAGATC | 267 |
| rs577407907 | snp | G/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426948 | AGTTTTATTCCTTTT[G/T]CATCCCCAGGGCCTG | 267 |
| rs577543467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56386633 | TCTATTCTACAAAAA[A/G]GCTTGTAGACTAACA | 267 |
| rs577589323 | snp | C/G | 0.00119737 | 0.0244387 | missense, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425204 | CCGGCTCGCCGGGGC[C/G]GGCCTCGGGCTGGCT | 267 |
| rs577604736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56393280 | ATTGTAAAGACCATC[A/G]AGGCTAGGAAGAAAT | 267 |
| rs577640400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56422777 | TTTTGCCATATTACT[A/G]AGGGTAGGGGAAAGT | 267 |
| rs577650282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424361 | CAGGTAAAGGCAGCA[A/G]AAAAGGAAGCACAGT | 267 |
| rs577690271 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412982 | CTGTTCACAATGGCA[C/T]CCAAGGGCTCAACCA | 267 |
| rs577703010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56405858 | GTGGGCATGGTGGCA[C/T]GTGCCAGTAGTCCCA | 267 |
| rs577778470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56398897 | GGAGCAGAGAGGGAC[C/T]TGCTATATACTGGAG | 267 |
| rs577783462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56423493 | TAGAATCTGAACATG[A/G]CTTTTATCAAAATAA | 267 |
| rs577832958 | in-del | -/CGGGCACCCAGCATCAT | 0.00318978 | 0.0398085 | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425675 | CCTCAGGCCGGGGGG[-/CGGGCACCCAGCATCAT]CGGGCACCCAGCATC | 267 |
| rs577846648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | AMFR | GRCh38.p7 | 16:56406718 | AAGAAATGATTTAGT[C/T]TAAAATATCAAATCT | 267 |
| rs577911096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56413233 | ATTTTTACTTTAAAA[C/T]ATACCATGCCAGGCA | 267 |
| rs577918321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56399687 | GACTATGGGGCACTA[C/T]TGTGGAGTGATAAAA | 267 |
| rs577923921 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | AMFR | GRCh38.p7 | 16:56421323 | CAGCCAATTTTTCTC[C/T]AAAGTGCTCTCAGAT | 267 |
| rs577990405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56408304 | TGATATTTAGAGATC[C/T]GTGTCATTTAATTTA | 267 |
| rs578042482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | AMFR | GRCh38.p7 | 16:56371464 | TTTTTAAAGGAGGTC[A/G]GTGGGGTGGTCCAGC | 267 |
| rs578160120 | snp | C/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362265 | GCTTTGGACTGGAGG[C/T]TCGGAAAGTCAGTCC | 267 |
| rs578187994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | AMFR | GRCh38.p7 | 16:56392742 | TCTATGTCTGATTGG[C/T]GTACCTGAAAGTGAC | 267 |
| rs745325348 | snp | C/T | 1.75219e-05 | 0.00295984 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362856 | TTGGGACAGGCCTCC[C/T]CCAGTCAGTCGGGCA | 267 |
| rs745512538 | snp | C/T | 3.35756e-05 | 0.00409716 | intron-variant | AMFR | GRCh38.p7 | 16:56401886 | AACCTCAGTCAGTTC[C/T]ACACGCACACTAAAC | 267 |
| rs745540710 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400315 | TAATTTTTTTGTATT[C/T]TTAGTAGAGGTGGGG | 267 |
| rs745548011 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380524 | GATTTTCTTTTCTAT[C/T]GCATTGTCAAGCTGC | 267 |
| rs745602556 | snp | A/G | 1.6604e-05 | 0.00288127 | intron-variant | AMFR | GRCh38.p7 | 16:56414365 | AACAAATCAGAGAAA[A/G]GAAGTTTATTTCTTC | 267 |
| rs745603835 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56408542 | ATTAGGGCTAGCACA[A/T]TTGAAATGCAATCCA | 267 |
| rs745605859 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56378292 | AAACCCACATAGCTG[A/G]GTTGACAGCTATACT | 267 |
| rs745616969 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421806 | CCAGAAATGAGTAAC[A/T]AAATAAAAACTCATC | 267 |
| rs745670918 | snp | C/T | 1.65209e-05 | 0.00287405 | synonymous-codon | AMFR | GRCh38.p7 | 16:56405041 | GAGGTGAATTACGTA[C/T]CTGTAATGAAGAGAG | 267 |
| rs745743533 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56404693 | TCCCAGGACAGCAAA[C/T]ACCTCCTGAGTTAGG | 267 |
| rs745763812 | in-del | -/A | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426338 | GAACGAACCTTAAAC[-/A]ACGTGCTAAGTCAAA | 267 |
| rs745775545 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388739 | TAAGATACAAACACA[C/T]GCATTAGCCTAAGCC | 267 |
| rs745778867 | snp | C/T | 2.12267e-05 | 0.00325774 | intron-variant | AMFR | GRCh38.p7 | 16:56385878 | CTGTTCTTTCCCTCC[C/T]AATTCCCAGTGATCT | 267 |
| rs745866987 | in-del | -/TA | | | intron-variant | AMFR | GRCh38.p7 | 16:56398319 | TATAAATGTATCATT[-/TA]TATATATATAAATGT | 267 |
| rs745868847 | snp | C/T | 3.33122e-05 | 0.00408105 | synonymous-codon | AMFR | GRCh38.p7 | 16:56405212 | CACTCACCGTAAAAT[C/T]ACATGAGCAGTCCTC | 267 |
| rs745886735 | snp | G/T | 6.59098e-05 | 0.00574026 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369292 | CAGTACCAGATGGTA[G/T]GGAACCTGGGGAAAC | 267 |
| rs745966114 | snp | A/C | 1.67069e-05 | 0.00289019 | missense | AMFR | GRCh38.p7 | 16:56389364 | TGTTCTAGCCAGGAA[A/C]GAAGACAGGAGCTAC | 267 |
| rs745994154 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377867 | CTTTATATTAGCGCC[C/T]ACAAAACAAAATAGG | 267 |
| rs746007351 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56389904 | CTTATCTGGCACCAA[A/T]CTTACTAAGACCTCC | 267 |
| rs746062672 | snp | A/C | 2.25207e-05 | 0.00335557 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362095 | GCTTTAGCACTGCCT[A/C]ATTTACTTCACCAAT | 267 |
| rs746062824 | snp | A/G | 4.98757e-05 | 0.00499353 | missense | AMFR | GRCh38.p7 | 16:56363925 | AAGCGACTCACTTGC[A/G]AGCTTGCTGGAGGAG | 267 |
| rs746073550 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56417221 | TCAAGACCAGCCTGG[C/G]CAACATAGTGAAACC | 267 |
| rs746098911 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402059 | TAATGGTTGCTAGGC[C/T]GAGCGCGGTGGCTTA | 267 |
| rs746109837 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56378803 | AATAGATACTTCACC[A/G]AAGATAGATGTACAG | 267 |
| rs746120333 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379554 | CAAAAGTCCAAAGTA[C/T]AACATCTCATCTGAG | 267 |
| rs746142423 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416145 | ATGTAGTCAGTCATA[C/T]GAATTTAAAAAATAA | 267 |
| rs746239100 | in-del | -/AA | 1.67683e-05 | 0.00289549 | intron-variant | AMFR | GRCh38.p7 | 16:56403128 | AAATAACTTAGAGAG[-/AA]AGAGAATAAAACACA | 267 |
| rs746312814 | snp | C/T | 3.31422e-05 | 0.00407063 | missense | AMFR | GRCh38.p7 | 16:56389220 | TTGTGTTGGTTTAAG[C/T]GAGGTCTCCCTTCGG | 267 |
| rs746336371 | snp | A/G | 3.38914e-05 | 0.00411638 | intron-variant | AMFR | GRCh38.p7 | 16:56409394 | CAAACGTGGTGACTA[A/G]GCAAGCAAAAAGCTT | 267 |
| rs746355366 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373531 | TTACGCAGTACATCA[C/T]GTTCAACTATCATGA | 267 |
| rs746383532 | snp | C/T | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424384 | AGCACAGTTTGGTGT[C/T]TGTTTCATTACACAG | 267 |
| rs746401076 | snp | C/T | 8.86564e-05 | 0.00665735 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408096 | GTGGCTGCTCATCGG[C/T]GTGGTGGGCGAGAAG | 267 |
| rs746437026 | in-del | -/AA | 7.20669e-05 | 0.00600235 | intron-variant | AMFR | GRCh38.p7 | 16:56414203 | CATAATACAAAGTTT[-/AA]AAAAAAAAATCTAGT | 267 |
| rs746455449 | snp | A/C | 1.77401e-05 | 0.00297821 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362643 | TCCTGATCGTCCCCC[A/C]CCCCAAGCAGTCCAG | 267 |
| rs746467199 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382423 | GAGCAAGGGTATCCA[A/G]TATTTTGGCTTCCCT | 267 |
| rs746531745 | snp | A/T | 1.64741e-05 | 0.00286998 | missense | AMFR | GRCh38.p7 | 16:56369261 | TTTCAACTGAGCGTG[A/T]CAGCTGGAGGTCCTG | 267 |
| rs746583510 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56383192 | CTTTTCCAGCTAATC[-/A]ATCACTCCCACTCTG | 267 |
| rs746636525 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372368 | CTCCAGGTTCATTCA[C/T]GCTGCAGCATGCAAC | 267 |
| rs746657499 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56423005 | TTTTGTCTTGCTTGG[A/C]CTTGGCAGGCAGTGT | 267 |
| rs746657833 | snp | C/T | 7.10353e-05 | 0.00595925 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362760 | AAGGATTAAATTTAT[C/T]AGCTGTCCAAACACT | 267 |
| rs746670484 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383444 | ATGTCACCTCCAGGC[A/G]TCAATCTCCCAAATG | 267 |
| rs746689427 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371169 | AACCTCTAAAATCAG[A/G]TAAAACTTCTCTTTA | 267 |
| rs746751700 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388983 | CTGTAGTAAATACCA[A/G]ACTACAGGAATTTTT | 267 |
| rs746757607 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406203 | TAAGTCTCTCATGGC[-/T]TTTTTTTTTTTTTTT | 267 |
| rs746832809 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397964 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
| rs746894812 | snp | G/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426443 | CAGACACAGAAAGTT[G/T]ATTAATGATTGCTTA | 267 |
| rs746897476 | snp | C/T | 1.65217e-05 | 0.00287412 | missense | AMFR | GRCh38.p7 | 16:56405037 | CCCAGAGGTGAATTA[C/T]GTATCTGTAATGAAG | 267 |
| rs746936980 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416337 | AAAAAAACAAATTTA[C/G]GGTCACTTAAACATT | 267 |
| rs746984424 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390092 | CTCTCTCAGGAGATG[A/G]TAATGCCTTAATTAT | 267 |
| rs747031959 | snp | C/G/T | 3.30274e-05 | 0.0040636 | missense | AMFR | GRCh38.p7 | 16:56404944 | TGAGGTCCAGGGACA[C/G/T]GAGAGTGAGCTCCAT | 267 |
| rs747096947 | snp | A/G | 1.71472e-05 | 0.00292802 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408084 | CAGGACTCGACCGTG[A/G]CTGCTCATCGGCGTG | 267 |
| rs747167232 | snp | A/G | 1.68749e-05 | 0.00290468 | missense | AMFR | GRCh38.p7 | 16:56362952 | CGTTCCGCGGCGGCA[A/G]CCAGCATCCTTCGAC | 267 |
| rs747208777 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56405110 | TTTAACCATGTTGTA[A/G]TTTAGTCCGATTTTT | 267 |
| rs747258763 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368474 | TTAATAGATTTCCAC[A/G]TATTTTTACATACTA | 267 |
| rs747259762 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403181 | TGCTAGTGATGAAGG[C/T]GCAGTATGCAGCGGA | 267 |
| rs747289090 | snp | A/G | 1.69997e-05 | 0.0029154 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389189 | AACCAACTAACCATC[A/G]AAATGGAAGAAGTGA | 267 |
| rs747339125 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | AMFR | GRCh38.p7 | 16:56403047 | AATTCGACGTTGCAC[C/T]TCATGAAACAGGTAA | 267 |
| rs747427208 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56419638 | TGTCTACTAAAAATA[A/C]AAAAAATTAGCTGGG | 267 |
| rs747464851 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373731 | GGCAGCATGAGCAGG[C/T]AGATGGAAATCTTAA | 267 |
| rs747478265 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375170 | TTAAAACGTTATATT[A/T]TTAATTTTCTTTTTT | 267 |
| rs747488963 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370127 | GTAAGAAACCTGCAC[-/T]TTGTAACCTGTAAAC | 267 |
| rs747578864 | snp | C/G | 0.000171744 | 0.00926512 | intron-variant | AMFR | GRCh38.p7 | 16:56364154 | TGAGCACAGGCCTCC[C/G]TCCTAAGCAGGTTCC | 267 |
| rs747615442 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56423274 | TAAACACGTGGAGAC[C/G]CCAGAGGAAAGATGG | 267 |
| rs747662298 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56408258 | TTACTATATGGTCCT[A/G]TTCTCCAATAACCCA | 267 |
| rs747687451 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56397020 | GGCGATCATTAAAAA[-/G]GAAACAACAGGTGCT | 267 |
| rs747702383 | snp | A/T | | | downstream-variant-500B | AMFR | GRCh38.p7 | 16:56361013 | TTTAAGCTACTTAAT[A/T]AGCTCCTGCTCTAAA | 267 |
| rs747712249 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56385149 | TGTCACCCAGGCTGT[A/G]GTGCAATGGTGTGAG | 267 |
| rs747757510 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373498 | ACATCACGACAGGCC[C/T]GTTCACCACAGTCCT | 267 |
| rs747763305 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | AMFR | GRCh38.p7 | 16:56369240 | CTAAAATATTGTCTG[C/T]TGTTATTTCAACTGA | 267 |
| rs747792714 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412147 | ATCATTTTAGATATT[C/T]GATGTCTTTGCCTCT | 267 |
| rs747835451 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378950 | AACCAAATGCTGGAG[A/T]GGATGTGGAGTAACA | 267 |
| rs747853071 | snp | C/T | 5.03436e-05 | 0.0050169 | intron-variant | AMFR | GRCh38.p7 | 16:56369144 | CCTACAGTATTCAAT[C/T]TTTGTGAAGATAGAA | 267 |
| rs747869873 | snp | G/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425899 | CCAGCACTCCTAGGG[G/T]CCGCGCAGCTTCCCT | 267 |
| rs747923202 | snp | A/G | 0.000104559 | 0.00722969 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362878 | AGTCGGGCACAGGGC[A/G]CAGGAGGCAGCTGAG | 267 |
| rs748107449 | snp | C/G | 1.78188e-05 | 0.00298481 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362416 | GTGCATGAGCCCGTG[C/G]GTCTGGCCTCTGGCA | 267 |
| rs748143647 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379509 | CATGCCTTCCCAACA[A/G]TCCCCCAAAGTCTTA | 267 |
| rs748153765 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417675 | AAAATGAAACTACCT[C/T]CAGGGTATGTGTATG | 267 |
| rs748179413 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56368406 | ATATCTCAGCCCATG[-/T]GACTGAGTCTATGCT | 267 |
| rs748278355 | snp | A/G | 1.77423e-05 | 0.00297839 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362301 | GTAGTGGGACAGAAA[A/G]GGGTGACTTCATCAC | 267 |
| rs748290917 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56369766 | GGAATCAACCTAAGC[A/G]TCCTTCAACACAGGA | 267 |
| rs748291710 | snp | A/T | 4.46419e-05 | 0.00472429 | intron-variant | AMFR | GRCh38.p7 | 16:56386042 | AACAAACAAGAATCC[A/T]GTGTAAGTTTCAGAG | 267 |
| rs748323153 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400810 | ATACTTTAAAATTCA[C/T]AAATATGCCTGGTTC | 267 |
| rs748347222 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387533 | GATGCGAATAGCACT[A/G]CTGCTAACAAAATTC | 267 |
| rs748362578 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427439 | GGCAATCTTTATTCA[A/G]TCCTAGCCACAGTAG | 267 |
| rs748400312 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386536 | ACTCACTTGGAGGCA[A/T]TTTCACATTTACTTT | 267 |
| rs748437561 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56407849 | AATGCTTGTTAAAAT[A/G]AAAGACCAAATATCC | 267 |
| rs748450371 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413653 | TTTCCAATGTCAGAC[A/T]ATCTCACCCAAAACA | 267 |
| rs748456777 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388212 | TACGATATAGTCTAT[C/T]GTTCTAGGCTACAAT | 267 |
| rs748628871 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56399105 | AAAACAAAATTCACC[A/G]TAATAAGAAAACACT | 267 |
| rs748633685 | snp | A/T | 1.67402e-05 | 0.00289306 | missense | AMFR | GRCh38.p7 | 16:56364056 | TCCACCTCGCCGAAG[A/T]CCAGCGTCTCCTCCA | 267 |
| rs748662382 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56400692 | TTTGTTGACTTAACT[A/C]CTACTTATCCTCAAG | 267 |
| rs748719351 | snp | C/T | 1.65141e-05 | 0.00287346 | missense | AMFR | GRCh38.p7 | 16:56363964 | TACGCTGCACCAGCA[C/T]GCGCTGTCTCTCATC | 267 |
| rs748749984 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412349 | GAGCTGGATAAGAAA[C/T]ATGCTCATTATAATT | 267 |
| rs748865182 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375049 | AAAATAAACGAATTA[A/G]TTGCAAATGTATATT | 267 |
| rs748899707 | snp | C/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361477 | TTTTTATTATTATTA[C/T]TGTTTTACAATAAAA | 267 |
| rs748957207 | snp | A/T | 0.000106564 | 0.00729869 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362725 | GGGAAGAGAAATGTC[A/T]CATAGAAAGTATTAC | 267 |
| rs749008653 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | AMFR | GRCh38.p7 | 16:56403063 | TCATGAAACAGGTAA[C/T]GCAGCTGCATAAAGA | 267 |
| rs749037114 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56418529 | AAAAAACAAAAAAAC[A/G]CCAGGCGCACTGGCT | 267 |
| rs749104432 | snp | A/T | 4.16875e-05 | 0.00456531 | intron-variant | AMFR | GRCh38.p7 | 16:56385888 | CCTCCTAATTCCCAG[A/T]GATCTTCTTAAAGCA | 267 |
| rs749134847 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370922 | AGCTCCTAGGGACAC[A/G]TTGTTCTGACTATAG | 267 |
| rs749166615 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380376 | CCTCTGGGCCTGTGA[C/T]GAGAGGGGGCTGCTG | 267 |
| rs749181443 | snp | A/C | 6.75493e-05 | 0.0058112 | intron-variant | AMFR | GRCh38.p7 | 16:56414390 | TTCTTCCTGCTGAAA[A/C]ATAAAAGCAGCTCTA | 267 |
| rs749204924 | snp | A/G | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362367 | AGGTATCGAACCAAG[A/G]GTTCCTTTTCCAAGA | 267 |
| rs749266682 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387638 | CAACAGCAGCTTAAT[C/G]TGAATTAAGGAAGGA | 267 |
| rs749296420 | snp | C/T | 3.53907e-05 | 0.00420644 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362794 | AGACCACATGCTTTA[C/T]ACAGCGGCAATGCAG | 267 |
| rs749300282 | snp | A/G | 6.39448e-05 | 0.00565405 | intron-variant | AMFR | GRCh38.p7 | 16:56386035 | ACCCTGAAACAAACA[A/G]GAATCCAGTGTAAGT | 267 |
| rs749306144 | snp | A/T | 1.80762e-05 | 0.00300629 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362208 | ACCCATGGGGCACAC[A/T]CATGAGATGCAGGAG | 267 |
| rs749309414 | in-del | -/CTC | 1.65106e-05 | 0.00287316 | intron-variant | AMFR | GRCh38.p7 | 16:56401726 | TGGCCCTTCACAAAG[-/CTC]CTACTTGTGGAAAAG | 267 |
| rs749420726 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422589 | TCCCCACGCCAGACC[A/G]AGCTCCACATGCTGG | 267 |
| rs749424943 | snp | C/G | 1.70574e-05 | 0.00292035 | missense | AMFR | GRCh38.p7 | 16:56405238 | TCCTCACTGTCACAA[C/G]AAGAGACTATAAAAA | 267 |
| rs749505738 | snp | C/T | 1.77631e-05 | 0.00298014 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362279 | GCTCGGAAAGTCAGT[C/T]CCAGATGTAGTGGGA | 267 |
| rs749524477 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56415279 | CAAAAGGACCTTGAT[A/G]AAAACAGTACAGATG | 267 |
| rs749555196 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388590 | TTTTTAACTTTTTGA[C/T]TCTTGTAGTAACACT | 267 |
| rs749559648 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416096 | CCAGCTTTATTACGA[C/T]GCAATTTCTTAAAAT | 267 |
| rs749675279 | snp | A/G | 7.09597e-05 | 0.00595608 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362636 | CACTTCCTCCTGATC[A/G]TCCCCCACCCCAAGC | 267 |
| rs749680213 | snp | C/T | 1.66713e-05 | 0.0028871 | intron-variant | AMFR | GRCh38.p7 | 16:56409419 | AAGCTTGGCTAAAAA[C/T]TCACATATTCAAATC | 267 |
| rs749832805 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56414778 | TAGTAAAACCCAGCA[C/T]CCAGAGATTCTGCCC | 267 |
| rs749874726 | in-del | -/C | 2.24349e-05 | 0.00334917 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362104 | CTGCCTAATTTACTT[-/C]ACCAATGAATGAAAA | 267 |
| rs749926435 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56421502 | AATTCACTTTTATCC[A/C]CTTTTGTTTGTGGTC | 267 |
| rs749982293 | snp | C/T | 1.66208e-05 | 0.00288273 | missense | AMFR | GRCh38.p7 | 16:56408051 | ACAGCAGGAAAGCAG[C/T]ATGGCAACCAACAGG | 267 |
| rs749994172 | snp | C/T | 0.00113572 | 0.0238027 | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425351 | CGGCGACCTCTGGCC[C/T]CCAGGCTTCCCTGCG | 267 |
| rs750043281 | snp | C/G | 1.70988e-05 | 0.00292389 | missense | AMFR | GRCh38.p7 | 16:56362920 | AGCGCTAGGAGGTCT[C/G]CTGCTTCTGAAGCCT | 267 |
| rs750070981 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56401532 | CTATGGGTGGGAAAC[A/G]GTCCTATGATGTAGG | 267 |
| rs750088166 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56365080 | TAGGCTGTGACAGAA[C/T]GGAGGTGGGTGCAGC | 267 |
| rs750107892 | snp | A/C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56415809 | ATCCTGGCACTTTGG[A/C/G]AGACCAAGGTGGGAG | 267 |
| rs750153726 | snp | A/G | 5.33537e-05 | 0.00516469 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362268 | TTGGACTGGAGGCTC[A/G]GAAAGTCAGTCCCAG | 267 |
| rs750243649 | snp | G/T | 1.65924e-05 | 0.00288027 | missense | AMFR | GRCh38.p7 | 16:56364033 | CTTCCACCTCACTGG[G/T]CTCCACTTCCACCTC | 267 |
| rs750257203 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402409 | GGACAAATCAGAGGA[C/G]TAAGGCCCCCAGAGA | 267 |
| rs750263145 | in-del | -/T | 1.7067e-05 | 0.00292117 | intron-variant | AMFR | GRCh38.p7 | 16:56363877 | GCCTTCAGCCACTAG[-/T]TTTTGATCTGGATTA | 267 |
| rs750335894 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373127 | GTGGCTCCCCTGTAA[C/T]ACTGTGAGATTCAGT | 267 |
| rs750337415 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411025 | TCCTGTAAGTGTACA[C/T]TCCCATGGGCAGTGT | 267 |
| rs750357700 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56422864 | AATTGTGTTTGTTCA[A/T]GAAAAACCTCCTGTG | 267 |
| rs750362480 | snp | C/T | 3.30164e-05 | 0.00406289 | missense | AMFR | GRCh38.p7 | 16:56407991 | GAAAGCCAAGGTGTG[C/T]ATTCCGTGGGTGTAG | 267 |
| rs750387247 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56384379 | TAATGACATTGCAGG[C/T]GCTATGCTCACTACA | 267 |
| rs750401411 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372246 | CAACACTCCTATTTC[G/T]CCTCGCCTCGCCCCA | 267 |
| rs750455868 | snp | C/T | 1.7783e-05 | 0.00298181 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362391 | TCCAAGATGCCCTGC[C/T]GGCTCAGGGGTGCAT | 267 |
| rs750520693 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412039 | ATTATACATAATATA[C/T]GTGAAATGGTTAGAC | 267 |
| rs750565848 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411949 | AAAGTCACTTAACAT[C/T]CCTGTGCTTTAGTTT | 267 |
| rs750631855 | snp | C/T | 3.32099e-05 | 0.00407478 | intron-variant | AMFR | GRCh38.p7 | 16:56401853 | GCAAACCTGTGGAAA[C/T]AAAACAAGCCCAGCA | 267 |
| rs750713127 | snp | C/T | 1.65067e-05 | 0.00287282 | synonymous-codon | AMFR | GRCh38.p7 | 16:56414282 | TCGAAGAGGGCCAAA[C/T]ACAATACACTGGATG | 267 |
| rs750724852 | snp | G/T | 1.65751e-05 | 0.00287876 | intron-variant | AMFR | GRCh38.p7 | 16:56405164 | TTAAAATCAACTGTA[G/T]GAGTAGGCCTCCATC | 267 |
| rs750744117 | snp | C/T | 3.29658e-05 | 0.00405978 | missense | AMFR | GRCh38.p7 | 16:56369218 | AAAGGTACTTGAATC[C/T]GTCCTTCTAAAATAT | 267 |
| rs750751125 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56400115 | CTTCTCACTAACTCT[A/G]CTTCTACCACCAGAG | 267 |
| rs750861099 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406796 | TAAAAGTATATACTA[C/T]AGTATGAGCTGACGG | 267 |
| rs750875669 | in-del | -/AAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56382511 | ATAGCTGATGAGCTA[-/AAA]AAAAAAAAAAAAAAA | 267 |
| rs750887479 | snp | C/G | 3.32116e-05 | 0.00407488 | intron-variant | AMFR | GRCh38.p7 | 16:56369345 | ACAGGAATACAAATA[C/G]AGAGTCCACAGAAAC | 267 |
| rs750921686 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56386352 | AAGCCAGACAGGCAA[A/G]CTCTAGAACCCTTCA | 267 |
| rs750938438 | snp | C/T | 1.77458e-05 | 0.00297868 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362613 | CCTGCTGCAGGCAGG[C/T]GACTGCTCACTTCCT | 267 |
| rs750946639 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387897 | TTGAGCTAATTAAGT[-/G]TGCTCCTTGAAGGCA | 267 |
| rs751021531 | snp | A/C/G | 8.3339e-05 | 0.00645475 | intron-variant | AMFR | GRCh38.p7 | 16:56369361 | AGAGTCCACAGAAAC[A/C/G]TTCACTGTTAACAGT | 267 |
| rs751023583 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415962 | TTTAAGGTGATGAAA[C/T]AGATGCTAAAAAGAC | 267 |
| rs751063466 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367915 | GTGCTGCTGTTACCG[C/T]CCTTCTAGCCAGTTT | 267 |
| rs751124554 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56376483 | CCCAAAATACATGAA[A/G]ATTAAACAACACACC | 267 |
| rs751240638 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402467 | AGAGATCCAAGCTGT[C/T]CCCCTGGGTGCAAAG | 267 |
| rs751257913 | snp | C/T | | | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423988 | ACTTTCAACCCCAAA[C/T]GGGAACATGCAAGGA | 267 |
| rs751299795 | snp | C/G | 3.30945e-05 | 0.0040677 | missense | AMFR | GRCh38.p7 | 16:56401824 | TGACAGCCAGCTCCT[C/G]TGGAGTTGCAACTGC | 267 |
| rs751370774 | in-del | -/GGATATTTTCTTTTT | 1.75403e-05 | 0.00296139 | intron-variant | AMFR | GRCh38.p7 | 16:56405255 | AGAGACTATAAAAAA[-/GGATATTTTCTTTTT]AGTAAAATGTAGCAT | 267 |
| rs751376369 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56386116 | TAATGGCTGGTGTTC[A/G]CTGAGGGCTTCTTGT | 267 |
| rs751387600 | snp | A/C | 3.30967e-05 | 0.00406783 | intron-variant | AMFR | GRCh38.p7 | 16:56401705 | GGACAGAACACCTGT[A/C]CCACATGGCCCTTCA | 267 |
| rs751437440 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373431 | GGGCTCACTAAAAGA[C/T]GGAGCCCTAATCCCA | 267 |
| rs751450013 | snp | C/G | 1.84025e-05 | 0.0030333 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362184 | AAGGAAATGCTGAGA[C/G]GGGAGGGGACCCATG | 267 |
| rs751460538 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374255 | TACAAAAGGTGTAAA[C/T]GCACTTAATGGGAAC | 267 |
| rs751486823 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56412003 | TAATAACAGCATATA[A/C]CTCATAGAATTGTTG | 267 |
| rs751494058 | snp | A/G | 3.30978e-05 | 0.0040679 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364013 | GCTCCCACGAGCCTC[A/G]AAGTCTTCCACCTCA | 267 |
| rs751496552 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413110 | TGAACATAAAGTAAA[G/T]CTGCTGTTGTGCTTT | 267 |
| rs751616370 | snp | A/C/T | 1.65209e-05 | 0.00287405 | missense | AMFR | GRCh38.p7 | 16:56369194 | AAGCCCAGTTTTACC[A/C/T]GTGTAGGAAAAGGTA | 267 |
| rs751622841 | snp | A/G | 1.77407e-05 | 0.00297826 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362586 | GTACGCATGAGGCAG[A/G]AGTAGAAGCTGCCTG | 267 |
| rs751715853 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56397062 | GGAGAAATAGGAAAA[C/T]TTTTACACTGTTGGT | 267 |
| rs751758046 | snp | A/C | 1.6513e-05 | 0.00287336 | synonymous-codon | AMFR | GRCh38.p7 | 16:56409526 | CACTGTCTGGACATT[A/C]AGCACACCAAAGATG | 267 |
| rs751806672 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56419404 | AATCTACTAAACTAA[A/C]CTGACTAGTTCTGCA | 267 |
| rs751819043 | snp | A/T | 1.69591e-05 | 0.00291191 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362718 | TTCTAAGGGGAAGAG[A/T]AATGTCACATAGAAA | 267 |
| rs751908670 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56420907 | TCAGAACCTTGACAG[G/T]AGTTTCATATTTCTA | 267 |
| rs751959175 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421973 | CTGGAGAGGCCCCCT[A/T]GGGAGGAGGAAGTTT | 267 |
| rs751980694 | snp | C/T | 8.25117e-05 | 0.00642254 | stop-gained | AMFR | GRCh38.p7 | 16:56404999 | CGTCCCCTTTCCTTC[C/T]CACGTCCCTTCGTGG | 267 |
| rs751984429 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388261 | ATACTGAATGCTGTA[A/G]AGGCAATTATAACAC | 267 |
| rs752033182 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56407256 | TATTAGCCAATTAGC[C/T]TCAGTTTATCTAATA | 267 |
| rs752075072 | snp | A/C | 1.65056e-05 | 0.00287272 | intron-variant | AMFR | GRCh38.p7 | 16:56367560 | CCAAAAACAGTCCAG[A/C]GTCACACAGAAATCA | 267 |
| rs752077432 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56409788 | AGACACCCAGAAACT[-/A]ATCTGTAAACTTTGG | 267 |
| rs752139247 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409023 | GGCCCGGGGTGGAAA[C/T]AGTATAAACTACTCA | 267 |
| rs752168832 | snp | C/T | 1.68371e-05 | 0.00290143 | intron-variant | AMFR | GRCh38.p7 | 16:56404873 | CTGATTCTGAAAGGC[C/T]TGCCCTCTGTTAGAG | 267 |
| rs752200388 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372978 | CGACAGAGCAAGACT[C/T]GGTGTTAAAACAAAC | 267 |
| rs752212803 | snp | C/G | 1.89608e-05 | 0.00307896 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362166 | CCCAGGTCCAGACGG[C/G]ACAAGGAAATGCTGA | 267 |
| rs752213917 | in-del | -/CGCTGCCGCTGC | | | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425420 | CACGGGCTCTGGCGT[-/CGCTGCCGCTGC]CGCTGCCGCTGCCGC | 267 |
| rs752258437 | snp | A/G | 1.65778e-05 | 0.002879 | intron-variant | AMFR | GRCh38.p7 | 16:56405170 | TCAACTGTATGAGTA[A/G]GCCTCCATCACCTCC | 267 |
| rs752299778 | snp | C/T | 1.69035e-05 | 0.00290714 | intron-variant | AMFR | GRCh38.p7 | 16:56363900 | CTGGATTATGCCAGG[C/T]GGTCTGGAGAAGCGA | 267 |
| rs752301812 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56400007 | CACCCAACTGCCCAA[C/G]CTGCATAACTAGAGA | 267 |
| rs752349613 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386290 | GCACTTAGAAGTTAG[G/T]GGACTTGTCCAAGAT | 267 |
| rs752433028 | snp | A/C | 1.64901e-05 | 0.00287137 | missense | AMFR | GRCh38.p7 | 16:56409504 | GGCACCACATGACCA[A/C]CTCTTCCACTGTCTG | 267 |
| rs752476970 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375621 | AAGAAAAATATACCA[C/T]ACCAACACTAACCAA | 267 |
| rs752487353 | snp | A/G | 1.77395e-05 | 0.00297816 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362579 | GTGGGACGTACGCAT[A/G]AGGCAGGAGTAGAAG | 267 |
| rs752522954 | snp | A/G | 1.70148e-05 | 0.00291669 | intron-variant | AMFR | GRCh38.p7 | 16:56409373 | CATTACACAATTCAA[A/G]GTTGGCAAACGTGGT | 267 |
| rs752535873 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56415025 | AGAAGGAAAAGAAAA[-/C]CCGGCGAGAGGGGCC | 267 |
| rs752554837 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380187 | TGACTTCTGTGCACT[C/T]GCAGGCTCAACACCA | 267 |
| rs752571374 | snp | A/C/G | 3.3986e-05 | 0.00412214 | synonymous-codon | AMFR | GRCh38.p7 | 16:56363020 | GAGGAAGCTCTCTGA[A/C/G]GCCGCATCATCTTCA | 267 |
| rs752648442 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56412696 | GAAATTCCGTCTCTA[A/C]AAACACCTAAACAAT | 267 |
| rs752703803 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56414121 | ATATTAACAACTGGC[A/G]AATCTGGATAAAGGG | 267 |
| rs752768191 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419854 | TCATAGCTATAGTGC[C/T]GTCAAAGCTTCAAGT | 267 |
| rs752843074 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409211 | AGTAAGTAAACACTA[A/T]GGGGTTGGGAAGAAA | 267 |
| rs752846516 | snp | A/G | 1.84985e-05 | 0.0030412 | intron-variant | AMFR | GRCh38.p7 | 16:56364121 | CTGGACACGGGGCAG[A/G]AAGCAAGGAGGCAGC | 267 |
| rs752878925 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371862 | ACTGAACATGCACAG[C/G]CTTTCTTGTCATTAT | 267 |
| rs752886586 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56381815 | ACACAAATGTAAATT[A/T]TGGACTTTGGGTGAT | 267 |
| rs752898077 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421202 | CAATCCTCCACCTCC[C/T]GCCTCAGCCTCCGCC | 267 |
| rs752927806 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370807 | TCTATAAATGTTTAC[A/G]TTCAAGGTTTTATTT | 267 |
| rs752993455 | snp | A/G | 1.72024e-05 | 0.00293273 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362908 | GGAAGGCAAGGGAGC[A/G]CTAGGAGGTCTGCTG | 267 |
| rs753026531 | in-del | -/A | 3.32878e-05 | 0.00407956 | intron-variant | AMFR | GRCh38.p7 | 16:56369355 | AAATACAGAGTCCAC[-/A]GAAACGTTCACTGTT | 267 |
| rs753042317 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419165 | AGTAGCTGAGATTAC[A/G]GGCACCTGCCACCAT | 267 |
| rs753171961 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377471 | AATAGAGGGAAACTT[A/T]GTCACTGTGATAAAG | 267 |
| rs753253755 | in-del | -/CGGGCAGAATTGGGACAGGCCTCCTC | 1.75974e-05 | 0.00296621 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362831 | CGCTTTTCCATGGAG[-/CGGGCAGAATTGGGACAGGCCTCCTC]CGGGCAGAATTGGGA | 267 |
| rs753261391 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56377797 | ATACTACAGTCAATT[A/G]CTTTCCTATATACAG | 267 |
| rs753416488 | snp | A/T | 1.64768e-05 | 0.00287021 | missense | AMFR | GRCh38.p7 | 16:56389257 | CTACAGGAACCAAAT[A/T]CTCATCCAAGTTCTC | 267 |
| rs753418518 | snp | C/T | 5.11932e-05 | 0.00505905 | missense | AMFR | GRCh38.p7 | 16:56362928 | GAGGTCTGCTGCTTC[C/T]GAAGCCTCCGTTCCG | 267 |
| rs753449602 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363689 | GCAAGCGTGGCCAAA[G/T]GGGTCCATGGGAGAT | 267 |
| rs753451711 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377256 | AAATCCAACAACACA[G/T]AAAAATAATTATAAA | 267 |
| rs753472242 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56394576 | GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA | 267 |
| rs753531975 | snp | A/G | 8.91575e-05 | 0.00667614 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362490 | ATGTTACCCCACGAC[A/G]TGGGGGCGGGCTCAC | 267 |
| rs753640956 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415684 | GTACTTAAATCCTTC[A/T]AACAACCAGGAACAA | 267 |
| rs753716251 | snp | A/G | 3.55802e-05 | 0.00421768 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362397 | ATGCCCTGCTGGCTC[A/G]GGGGTGCATGAGCCC | 267 |
| rs753725587 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56382132 | AATGTGAGTGTCCAA[C/T]GACAGATTAATAGAT | 267 |
| rs753763997 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421439 | TTAAGACAAAAACAG[G/T]CCTAGTCAAATAGGT | 267 |
| rs753781061 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383235 | TGCACTTCTATGAGC[C/T]CATCTTGTAAGAATT | 267 |
| rs753782093 | snp | A/G | 1.67005e-05 | 0.00288963 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408062 | GCAGCATGGCAACCA[A/G]CAGGGACAGGACTCG | 267 |
| rs753786754 | snp | C/T | 2.04962e-05 | 0.0032012 | intron-variant | AMFR | GRCh38.p7 | 16:56408142 | CACAGTAGGAAACTG[C/T]TCATTCTTCTTCATG | 267 |
| rs753790652 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56369921 | ACAGAAACTCAAATA[C/T]CGTATGTTCTTATAA | 267 |
| rs753792099 | snp | C/G | 1.75718e-05 | 0.00296405 | intron-variant | AMFR | GRCh38.p7 | 16:56389139 | TAGTATCTGCTTAAG[C/G]GAGAACACCCCTTAG | 267 |
| rs753908507 | snp | A/G | 1.64743e-05 | 0.00287 | missense | AMFR | GRCh38.p7 | 16:56403010 | TGTTTCCAACCACAC[A/G]TAGATAGTTCTTGTG | 267 |
| rs753981968 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412357 | TAAGAAATATGCTCA[C/T]TATAATTACCTCTGG | 267 |
| rs753985555 | in-del | -/G | 3.36706e-05 | 0.00410295 | intron-variant | AMFR | GRCh38.p7 | 16:56409406 | CTAAGCAAGCAAAAA[-/G]CTTGGCTAAAAACTC | 267 |
| rs753986217 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56389632 | ATCTACCAAGCTCCT[C/T]GTTGTGACCCCTCTT | 267 |
| rs753994423 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56371954 | AAGTAGTCTAGAGAT[G/T]ATTTAAAATATATGG | 267 |
| rs754005411 | snp | C/T | 4.95786e-05 | 0.00497864 | synonymous-codon, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425253 | GATGATGGTGCCCAG[C/T]AGGGCCAGGCCGCTG | 267 |
| rs754122576 | in-del | -/AT | | | intron-variant | AMFR | GRCh38.p7 | 16:56365949 | CTCCATTATATATAC[-/AT]ATATATATATAAAAT | 267 |
| rs754130815 | snp | A/G | 1.77625e-05 | 0.00298009 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362744 | AGAAAGTATTACAAA[A/G]AAGGATTAAATTTAT | 267 |
| rs754134863 | snp | A/G | 1.69103e-05 | 0.00290773 | synonymous-codon | AMFR | GRCh38.p7 | 16:56385961 | CTGCGTAATGCCAAG[A/G]ATGTTGGTGGTGTGC | 267 |
| rs754250157 | in-del | -/AT | | | intron-variant | AMFR | GRCh38.p7 | 16:56416502 | CAAACTAAAGCACAA[-/AT]TGGTGCAATCTCCGC | 267 |
| rs754279103 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56417873 | GAAACATAACTGGAG[A/C]ATTCCTCATTTAAAA | 267 |
| rs754297048 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56391103 | GCACACAATCATTCC[A/G]GAAGTTACAAAGCAA | 267 |
| rs754410410 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379298 | CTCTTTTTAAAACCA[C/T]CATATCTCGTGAGAC | 267 |
| rs754430956 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56400427 | ACCCCTGAACCGCTG[A/C]AGCCATTACTAACCA | 267 |
| rs754433425 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402683 | TCATGACAAATAAGA[A/G]CCTAATACTGAGCAC | 267 |
| rs754458280 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383514 | GCCCACAGAGCAACC[C/G]AGACTTACCCAAATA | 267 |
| rs754486307 | snp | C/T | 1.6656e-05 | 0.00288578 | intron-variant | AMFR | GRCh38.p7 | 16:56401864 | GAAACAAAACAAGCC[C/T]AGCAGGAACCTCAGT | 267 |
| rs754494369 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56367604 | GGGAAACCCTGGTGT[C/G]CAGAGGGAGCTATGG | 267 |
| rs754500758 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416916 | AAAAAAAAAAAGTCT[C/G]AGTATACTGATACTA | 267 |
| rs754545318 | snp | G/T | 1.68046e-05 | 0.00289862 | missense | AMFR | GRCh38.p7 | 16:56363003 | GACGCACCTTCCGAG[G/T]GGAGGAAGCTCTCTG | 267 |
| rs754569282 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56373476 | TTCTTTCCCTCCCCC[A/G]ACACCTACATCACGA | 267 |
| rs754594767 | snp | A/C | 1.65124e-05 | 0.00287331 | intron-variant | AMFR | GRCh38.p7 | 16:56367571 | CCAGAGTCACACAGA[A/C]ATCAAATCACAGACT | 267 |
| rs754617852 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56393917 | ATACATTCTTCTCAC[A/C]ACCACACCACACCTA | 267 |
| rs754626272 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56384871 | TAATGGCCTAATCTC[A/G]GCTCACTGCAACCTC | 267 |
| rs754650644 | snp | A/G | 3.34197e-05 | 0.00408763 | intron-variant | AMFR | GRCh38.p7 | 16:56404900 | AGAGCTCCTTCTGAG[A/G]AAACTTACCAACATG | 267 |
| rs754774893 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412063 | GTTAGACAAGTGCCA[C/T]ACTAGGCACTAAGCA | 267 |
| rs754801349 | snp | A/G | 3.36559e-05 | 0.00410205 | missense | AMFR | GRCh38.p7 | 16:56408067 | ATGGCAACCAACAGG[A/G]ACAGGACTCGACCGT | 267 |
| rs754828852 | snp | A/G | 3.29489e-05 | 0.00405874 | missense | AMFR | GRCh38.p7 | 16:56389281 | AGTTCTCTCCTTGAT[A/G]TTCTTCCCTGACACG | 267 |
| rs754839373 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56412529 | AATTTCTGGTCCACA[A/G]ATAAAAAATTTGAAG | 267 |
| rs754892588 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56410603 | CATTATAATGAGGGC[C/T]GGGCGTGGTGGCTCA | 267 |
| rs754922563 | snp | C/T | 1.70292e-05 | 0.00291793 | missense | AMFR | GRCh38.p7 | 16:56362937 | TGCTTCTGAAGCCTC[C/T]GTTCCGCGGCGGCAG | 267 |
| rs754979121 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56418324 | GCCTGACCAACATGG[C/T]GCAACCCCATCTCTA | 267 |
| rs754988151 | snp | G/T | 3.49779e-05 | 0.00418183 | intron-variant | AMFR | GRCh38.p7 | 16:56389156 | AGAACACCCCTTAGG[G/T]ATAGTTTCAGAGGTT | 267 |
| rs755007179 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380042 | GCTCTGATCCCACAT[C/T]TGCCTTCCGCACTGC | 267 |
| rs755068171 | snp | C/T | 1.67158e-05 | 0.00289096 | missense | AMFR | GRCh38.p7 | 16:56364051 | CCACTTCCACCTCGC[C/T]GAAGTCCAGCGTCTC | 267 |
| rs755087019 | in-del | -/AAAT | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361588 | TTGAAAGATTTATTG[-/AAAT]AAATTATCTTTGCCT | 267 |
| rs755093790 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | AMFR | GRCh38.p7 | 16:56403023 | ACGTAGATAGTTCTT[C/G]TGCCGACGAATTCGA | 267 |
| rs755184874 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370778 | GGATTTTTTTTCCAC[A/G]TATGTAAATTAACTC | 267 |
| rs755191501 | in-del | -/TT | | | intron-variant | AMFR | GRCh38.p7 | 16:56384058 | CCAACCATAATGACC[-/TT]TTTCTCAGTTCCTAG | 267 |
| rs755191602 | snp | A/G | 1.81694e-05 | 0.00301403 | intron-variant | AMFR | GRCh38.p7 | 16:56364115 | CTCGGTCTGGACACG[A/G]GGCAGGAAGCAAGGA | 267 |
| rs755268195 | snp | C/G | 0.000106534 | 0.00729765 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362283 | GGAAAGTCAGTCCCA[C/G]ATGTAGTGGGACAGA | 267 |
| rs755297098 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56419417 | AACCTGACTAGTTCT[C/G]CAATTCCACATTATT | 267 |
| rs755304782 | snp | A/G/T | 1.84398e-05 | 0.00303637 | intron-variant | AMFR | GRCh38.p7 | 16:56405278 | TCTTTTTAGTAAAAT[A/G/T]TAGCATTGCTCAGGC | 267 |
| rs755346315 | snp | G/T | 1.77606e-05 | 0.00297993 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362747 | AAGTATTACAAAGAA[G/T]GATTAAATTTATCAG | 267 |
| rs755367836 | snp | A/G | 1.94956e-05 | 0.00312209 | intron-variant | AMFR | GRCh38.p7 | 16:56409613 | AAAAATGTTTATGAA[A/G]GTGAGTACCATCACA | 267 |
| rs755404628 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56377342 | TCAATTAATATACTT[A/C]TATATTATCAACAGG | 267 |
| rs755424872 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363827 | GCCGTTTCACTGTTG[C/G]CATCTGTTTAAAAAG | 267 |
| rs755466258 | snp | C/G | 4.99156e-05 | 0.00499553 | intron-variant | AMFR | GRCh38.p7 | 16:56401861 | GTGGAAACAAAACAA[C/G]CCCAGCAGGAACCTC | 267 |
| rs755475650 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56376149 | AACTGAGGCAAAAAT[C/T]AAAAGAACCACAAAG | 267 |
| rs755478440 | snp | C/G | 2.36264e-05 | 0.00343695 | synonymous-codon, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425268 | CAGGGCCAGGCCGCT[C/G]AGGCCCGTGTAGGTG | 267 |
| rs755530609 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56373894 | AAAAGCAGGCCAGGT[C/G]CAGCGGCTCACACCT | 267 |
| rs755553195 | in-del | -/CCATTACTAACCA | | | intron-variant | AMFR | GRCh38.p7 | 16:56400430 | CCTGAACCGCTGCAG[-/CCATTACTAACCA]ATCCCCCTGGATCTT | 267 |
| rs755567251 | snp | C/T | 4.95561e-05 | 0.00497751 | missense, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56414329 | TCAAAACACAGCAAG[C/T]GGTATTTACTAGAAC | 267 |
| rs755578889 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373505 | GACAGGCCTGTTCAC[C/T]ACAGTCCTTTTTACG | 267 |
| rs755581247 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386298 | AAGTTAGGGGACTTG[C/T]CCAAGATCACACAGT | 267 |
| rs755664198 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424245 | AACTGTGTTAGAATA[A/G]ATCCTCAAATAAGAA | 267 |
| rs755676620 | snp | C/T | 0.000762631 | 0.0195124 | intron-variant, missense | AMFR | GRCh38.p7 | 16:56388809 | CCACCTCCTGTCCCA[C/T]TGGAACGTCTTCAGG | 267 |
| rs755693424 | in-del | -/TC | | | intron-variant | AMFR | GRCh38.p7 | 16:56419057 | TAGACAGAGTCTCAC[-/TC]TGTCGCCCGGGCTGG | 267 |
| rs755814171 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374815 | AAGAGCATCAAAGAA[A/G]GTATAAATAAATAAA | 267 |
| rs755840452 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375629 | ATACCACACCAACAC[-/T]TAACCAAAAGAAACC | 267 |
| rs755885011 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363664 | AGGTTAGCACACAAG[C/T]GCTCTCTCGGCAAGC | 267 |
| rs755897893 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426739 | TCCCACCTTGCCTTC[A/G]CAAAGTGCAGGGATT | 267 |
| rs755962008 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56407673 | TGAAAAATTTTTAAA[C/T]CTTAAAATATTCATG | 267 |
| rs756051344 | snp | A/C | 0.000173948 | 0.00932437 | synonymous-codon | AMFR | GRCh38.p7 | 16:56386018 | CCAGCTCGCAATCCG[A/C]GACCCTGAAACAAAC | 267 |
| rs756110663 | snp | C/T | 1.77625e-05 | 0.00298009 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362374 | GAACCAAGAGTTCCT[C/T]TTCCAAGATGCCCTG | 267 |
| rs756123080 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370886 | TGCCTTAGGGGCACA[A/G]TAAAGCCCTCCTGAG | 267 |
| rs756140159 | snp | C/T | 3.30262e-05 | 0.0040635 | missense | AMFR | GRCh38.p7 | 16:56407996 | CCAAGGTGTGCATTC[C/T]GTGGGTGTAGCCGGT | 267 |
| rs756160419 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56399972 | CCGTCTTCCCAACCT[C/G]AACAAACAGCACCAC | 267 |
| rs756189419 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421248 | ACTGCCGGTGTGAAC[C/T]ACTGAACCCAGCCCT | 267 |
| rs756216374 | snp | C/T | 1.64969e-05 | 0.00287196 | missense | AMFR | GRCh38.p7 | 16:56401763 | CCACAGGGCAGTTTC[C/T]GCGCAGCCTGCATGG | 267 |
| rs756403470 | in-del | -/CCT | 2.14461e-05 | 0.00327454 | intron-variant | AMFR | GRCh38.p7 | 16:56385873 | TCTAGCTGTTCTTTC[-/CCT]CCTAATTCCCAGTGA | 267 |
| rs756454237 | snp | C/T | 1.648e-05 | 0.0028705 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369223 | TACTTGAATCCGTCC[C/T]TCTAAAATATTGTCT | 267 |
| rs756454867 | in-del | -/A | 3.64166e-05 | 0.00426696 | intron-variant | AMFR | GRCh38.p7 | 16:56405272 | TATTTTCTTTTTAGT[-/A]AAAATGTAGCATTGC | 267 |
| rs756465568 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373286 | GGAGAAACTACTCAA[C/T]CAGAACCTCATCTGC | 267 |
| rs756506049 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377799 | ACTACAGTCAATTGC[C/T]TTCCTATATACAGAA | 267 |
| rs756507757 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56389452 | GAGAATTCACCCAGA[A/G]GTACTCTGGATATAT | 267 |
| rs756559027 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388449 | CTAGGACATTACTGT[A/G]AACTCCTGCAGACTT | 267 |
| rs756563296 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400165 | TTTTAGATGGAGTTT[C/T]GTTCTTGTTGCCCAG | 267 |
| rs756583883 | snp | A/C | 1.81164e-05 | 0.00300963 | intron-variant | AMFR | GRCh38.p7 | 16:56409592 | GTCTTTGAGATGCTA[A/C]AAAAGAAAAATGTTT | 267 |
| rs756594231 | snp | A/C | 1.69143e-05 | 0.00290807 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362726 | GGAAGAGAAATGTCA[A/C]ATAGAAAGTATTACA | 267 |
| rs756617300 | snp | A/G | 5.32288e-05 | 0.00515864 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362614 | CTGCTGCAGGCAGGC[A/G]ACTGCTCACTTCCTC | 267 |
| rs756652357 | snp | C/G | 1.6609e-05 | 0.0028817 | intron-variant | AMFR | GRCh38.p7 | 16:56369347 | AGGAATACAAATACA[C/G]AGTCCACAGAAACGT | 267 |
| rs756683186 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416077 | TCCCCCAGCCAAACA[C/T]GCCCCAGCTTTATTA | 267 |
| rs756693448 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375988 | GCTTGAACCCAGGAG[A/G]TGGAGGTTGCAGTGA | 267 |
| rs756710106 | snp | A/C | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424373 | GCAGAAAAGGAAGCA[A/C]AGTTTGGTGTTTGTT | 267 |
| rs756732842 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56378448 | ATACTCTTCACAATA[A/C]TTAACTCAAAATGGA | 267 |
| rs756760711 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413468 | TGCAGTGAGCTGAGA[C/T]TGCGCCACTGCACTG | 267 |
| rs756812051 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427134 | ATTCCACTTTGGAAA[C/T]TTTAGAAACATCTTG | 267 |
| rs756822652 | snp | C/G | 3.29962e-05 | 0.00406165 | intron-variant | AMFR | GRCh38.p7 | 16:56407955 | CAAGTCCTGCATCCA[C/G]TATCTCACCTCTGCA | 267 |
| rs756873048 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56365052 | TGGCCAGGGTCAGCC[C/T]ATTGCCCGCTTCTAG | 267 |
| rs756879265 | snp | A/G | 1.65332e-05 | 0.00287512 | synonymous-codon, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56414341 | AAGCGGTATTTACTA[A/G]AACCTGTAAACAAAT | 267 |
| rs756911187 | snp | C/T | 3.54868e-05 | 0.00421214 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362768 | AATTTATCAGCTGTC[C/T]AAACACTATAAGACC | 267 |
| rs756915380 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56414723 | ACATTATTTTGACAG[C/T]CTTGAAGAAAACTGT | 267 |
| rs756925846 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363714 | GGAGATGACTGACAG[C/T]ACCAGCATCAGAGGT | 267 |
| rs756983668 | snp | A/G | 5.21744e-05 | 0.00510729 | missense | AMFR | GRCh38.p7 | 16:56385989 | TGCATCACTTCAACC[A/G]AAAAACTCGGCAGCC | 267 |
| rs757034181 | snp | A/G | 1.66463e-05 | 0.00288494 | synonymous-codon | AMFR | GRCh38.p7 | 16:56363923 | AGAAGCGACTCACTT[A/G]CGAGCTTGCTGGAGG | 267 |
| rs757094911 | snp | A/C | 1.77922e-05 | 0.00298258 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362262 | CCGGCTTTGGACTGG[A/C]GGCTCGGAAAGTCAG | 267 |
| rs757126819 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363691 | AAGCGTGGCCAAAGG[A/G]GTCCATGGGAGATGA | 267 |
| rs757132892 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400157 | TTTTTGTTTTTTAGA[C/T]GGAGTTTCGTTCTTG | 267 |
| rs757167791 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56394749 | AGCGAGACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 267 |
| rs757184813 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387543 | GCACTACTGCTAACA[A/G]AATTCCAGGGATGCT | 267 |
| rs757194244 | snp | C/T | 1.65861e-05 | 0.00287972 | intron-variant | AMFR | GRCh38.p7 | 16:56405186 | GCCTCCATCACCTCC[C/T]TCCCCAATTTCACTC | 267 |
| rs757206874 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390349 | TAAGGGCTCAAGTAG[A/G]CACTGAATAAAAATG | 267 |
| rs757221813 | in-del | -/A | 0.001514 | 0.027472 | intron-variant | AMFR | GRCh38.p7 | 16:56414203 | CATAATACAAAGTTT[-/A]AAAAAAAAAATCTAG | 267 |
| rs757230326 | snp | A/G | 6.62065e-05 | 0.00575316 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364016 | CCCACGAGCCTCGAA[A/G]TCTTCCACCTCACTG | 267 |
| rs757272379 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370925 | TCCTAGGGACACGTT[A/G]TTCTGACTATAGAAG | 267 |
| rs757287484 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411011 | AACTTCCAAAGCAGT[C/T]CTGTAAGTGTACATT | 267 |
| rs757287787 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56381301 | TACCTCCCACAACAC[A/G]TGGGAACTCAAGAGG | 267 |
| rs757316359 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383257 | GTAAGAATTCCACAC[A/G]CTTGACTCTTCCCTC | 267 |
| rs757329408 | snp | A/G | 1.69934e-05 | 0.00291486 | intron-variant | AMFR | GRCh38.p7 | 16:56409384 | TCAAAGTTGGCAAAC[A/G]TGGTGACTAAGCAAG | 267 |
| rs757340442 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56422689 | ACCTTCCATGAACCC[C/T]TCCCTGGGCACAATT | 267 |
| rs757342428 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409851 | CTATTCAAAGGATAG[C/T]GATATTAGTTTAGTA | 267 |
| rs757375641 | in-del | -/GAGCCCTT | | | intron-variant | AMFR | GRCh38.p7 | 16:56387330 | AAGTTTTACCTGGAA[-/GAGCCCTT]GAGCCCTTCATTCAC | 267 |
| rs757426713 | snp | A/T | 1.77413e-05 | 0.00297831 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362606 | GAAGCTGCCTGCTGC[A/T]GGCAGGCGACTGCTC | 267 |
| rs757466955 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56407467 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 267 |
| rs757560573 | snp | C/T | 1.68241e-05 | 0.00290031 | intron-variant | AMFR | GRCh38.p7 | 16:56404878 | TCTGAAAGGCTTGCC[C/T]TCTGTTAGAGCTCCT | 267 |
| rs757585106 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56394193 | CATACCAGAATCTCT[-/G]GGACACATTTAAGGC | 267 |
| rs757754654 | snp | A/G | 9.90377e-05 | 0.00703627 | intron-variant | AMFR | GRCh38.p7 | 16:56367564 | AAACAGTCCAGAGTC[A/G]CACAGAAATCAAATC | 267 |
| rs757768695 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56382512 | TAGCTGATGAGCTAA[-/AA]AAAAAAAAAAAAAAA | 267 |
| rs757771028 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402780 | AGGTTCTGTTTTCAT[C/T]CCTAATTTAGAGGTG | 267 |
| rs757803274 | snp | A/C | 0.000106648 | 0.00730154 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362522 | CTGTGCGCCTCCCCC[A/C]CACTCTTCCCACTGG | 267 |
| rs757839140 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417939 | AGGCCAAGGTGGGTG[A/T]GTTGCTTGAGTCCAG | 267 |
| rs757840419 | snp | C/G | 1.65045e-05 | 0.00287263 | missense | AMFR | GRCh38.p7 | 16:56405014 | CCACGTCCCTTCGTG[C/G]TTGAGGTCCCAGAGG | 267 |
| rs757857703 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56365217 | CGAGAGTCAAAGGAC[A/G]GGGGAACTGGTGGCT | 267 |
| rs757860102 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56415822 | GGGAGACCAAGGTGG[C/G]AGGACTGCTTGAGGC | 267 |
| rs757864801 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368132 | TTCCTCATCTCCTGC[A/G]AGGGATATGTTCTGC | 267 |
| rs757983335 | snp | C/G | 7.5553e-05 | 0.00614579 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362168 | CAGGTCCAGACGGGA[C/G]AAGGAAATGCTGAGA | 267 |
| rs758030819 | snp | C/T | 4.94915e-05 | 0.00497426 | synonymous-codon | AMFR | GRCh38.p7 | 16:56401765 | ACAGGGCAGTTTCCG[C/T]GCAGCCTGCATGGAG | 267 |
| rs758117068 | snp | C/T | 1.65734e-05 | 0.00287862 | intron-variant | AMFR | GRCh38.p7 | 16:56405174 | CTGTATGAGTAGGCC[C/T]CCATCACCTCCCTCC | 267 |
| rs758178311 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56422918 | TAAACTGTGCTCTAA[A/C]AAGATAAGTTTTGGG | 267 |
| rs758196891 | snp | C/T | 4.94238e-05 | 0.00497086 | missense | AMFR | GRCh38.p7 | 16:56389295 | TGTTCTTCCCTGACA[C/T]GATTATTGTCGGCAA | 267 |
| rs758199907 | in-del | -/CATTTATCATGCTTTA | 1.67332e-05 | 0.00289246 | intron-variant | AMFR | GRCh38.p7 | 16:56369162 | TGTGAAGATAGAACC[-/CATTTATCATGCTTTA]AAAGCCCAGTTTTAC | 267 |
| rs758202136 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372247 | AACACTCCTATTTCG[C/T]CTCGCCTCGCCCCAG | 267 |
| rs758218653 | snp | A/G | 1.67851e-05 | 0.00289694 | intron-variant | AMFR | GRCh38.p7 | 16:56363910 | CCAGGTGGTCTGGAG[A/G]AGCGACTCACTTGCG | 267 |
| rs758454597 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56377716 | GTAGAAAATCTGGAA[-/G]AACTGATAAAAACAC | 267 |
| rs758457891 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56373254 | GGGCACACTGTTCTT[A/C]ACAACGTCTGCCCTC | 267 |
| rs758473807 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411985 | TCCATACAATAGGTC[G/T]TATAATAACAGCATA | 267 |
| rs758482732 | snp | G/T | 1.73703e-05 | 0.00294701 | intron-variant | AMFR | GRCh38.p7 | 16:56389169 | GGTATAGTTTCAGAG[G/T]TTGAAACCAACTAAC | 267 |
| rs758526313 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56404008 | ATCTTTGGCCATTTG[C/T]TTGTCCCCTTTTTGA | 267 |
| rs758539823 | snp | A/C | 1.64947e-05 | 0.00287177 | intron-variant | AMFR | GRCh38.p7 | 16:56367540 | CCGCTGGAAGAGAAA[A/C]AGTACCAAAAACAGT | 267 |
| rs758648077 | snp | C/T | | | stop-gained | AMFR | GRCh38.p7 | 16:56405024 | TCGTGGTTGAGGTCC[C/T]AGAGGTGAATTACGT | 267 |
| rs758757551 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417358 | AAGGCTGCAGGGAAC[C/T]GTGATTGCACCACTG | 267 |
| rs758845503 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56418084 | GTGGGAGAATCACCC[C/T]AGACACAGGGAGGTT | 267 |
| rs758869259 | in-del | -/A | 1.68216e-05 | 0.00290009 | intron-variant | AMFR | GRCh38.p7 | 16:56414387 | TATTTCTTCCTGCTG[-/A]AAAATAAAAGCAGCT | 267 |
| rs758870702 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386402 | TCCAGGGGGGCTGGA[C/T]GCAGCCCAGCCCAGC | 267 |
| rs758932298 | snp | A/G | 9.41664e-05 | 0.00686107 | intron-variant | AMFR | GRCh38.p7 | 16:56364129 | GGGGCAGGAAGCAAG[A/G]AGGCAGCTGTGAGCA | 267 |
| rs758933205 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387204 | TCATGTACTAACTAG[A/G]GAGAAATAAAGTTGA | 267 |
| rs758990384 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56407179 | GAATGCTATCAAACA[A/G]AAATAAACTTTAACT | 267 |
| rs759176795 | snp | A/G | 1.65056e-05 | 0.00287272 | synonymous-codon | AMFR | GRCh38.p7 | 16:56401786 | CTGCATGGAGTCCCA[A/G]CAGATGGCACAGTCG | 267 |
| rs759211593 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56386266 | TACCCTTGGTCTTTG[A/G]TCTCTGAGGCACTTA | 267 |
| rs759237194 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56404180 | CTGGGATTACAGGCA[C/T]GAGCCACCGCGTCCA | 267 |
| rs759239947 | snp | A/G | 1.65307e-05 | 0.0028749 | synonymous-codon | AMFR | GRCh38.p7 | 16:56363995 | AGCAGACTTGGAGAA[A/G]CGGCTCCCACGAGCC | 267 |
| rs759258250 | in-del | -/CACACACACG | | | intron-variant | AMFR | GRCh38.p7 | 16:56365593 | ACATGTAGGTACATA[-/CACACACACG]CACACACACGCTGGA | 267 |
| rs759297090 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56369138 | AGTTAACCTACAGTA[C/T]TCAATCTTTGTGAAG | 267 |
| rs759315081 | in-del | -/CC | | | intron-variant | AMFR | GRCh38.p7 | 16:56365599 | GGTACATACACACAC[-/CC]ACGCACACACACGCT | 267 |
| rs759327896 | snp | C/T | 1.70522e-05 | 0.0029199 | intron-variant | AMFR | GRCh38.p7 | 16:56363880 | TTCAGCCACTAGTTT[C/T]TGATCTGGATTATGC | 267 |
| rs759390727 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375923 | ATTAGTTGGGTGTGG[G/T]GGCACACGCCTGTAA | 267 |
| rs759412449 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375549 | AACCAAGACCTAACT[C/G]AATGTTGTTTACCCA | 267 |
| rs759458808 | snp | C/T | 1.68966e-05 | 0.00290655 | intron-variant | AMFR | GRCh38.p7 | 16:56403136 | TAGAGAGAAAGAGAA[C/T]AAAACACACGGTAAA | 267 |
| rs759479474 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon | AMFR | GRCh38.p7 | 16:56409490 | TCCGGCAAACCAGAG[A/G]CACCACATGACCACC | 267 |
| rs759487939 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415523 | ATGCCATCCCTCCTT[A/T]GGGAGAACACTTAAG | 267 |
| rs759497923 | snp | A/G | 1.7741e-05 | 0.00297829 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362667 | AGTCCAGTCAACACC[A/G]GAAGAGATCATACCT | 267 |
| rs759539083 | in-del | -/C | 0.000452528 | 0.0150353 | intron-variant | AMFR | GRCh38.p7 | 16:56389401 | GTCCAAAAGAAGATA[-/C]GTCAGCATCCTTGAT | 267 |
| rs759617526 | snp | C/T | 3.36423e-05 | 0.00410122 | missense | AMFR | GRCh38.p7 | 16:56362967 | GCCAGCATCCTTCGA[C/T]GCAGGGTCACGGGGT | 267 |
| rs759667536 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413885 | CAATATTGGGACAAC[C/T]TGGCTACACTGAATA | 267 |
| rs759748118 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382929 | GGCACATGGGAAAAG[A/G]AAGGGAGCATGACTT | 267 |
| rs759803147 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56381722 | AAAGGCAGAGTGCAT[A/T]CAGAATCTTTAGGGC | 267 |
| rs759833707 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421047 | CCATCTGAGAGCACT[C/T]TAGAGAAAAATTGGC | 267 |
| rs759848138 | in-del | -/ACA | 5.35776e-05 | 0.00517551 | utr-variant-3-prime, cds-indel | AMFR | GRCh38.p7 | 16:56362448 | AGTCTACATGCTTCC[-/ACA]ACAACGACAGCAGTT | 267 |
| rs759875872 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56414950 | TAAATGTTCTCCATG[C/T]TTGGTGTTGGCTTTG | 267 |
| rs759908267 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422293 | TCCACCCTTCTCTCT[C/G]AAATGGATCCCCAGG | 267 |
| rs759943408 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409054 | GAAAGAAGAGCTCCA[C/T]GAACCAGAGTAAGCT | 267 |
| rs759959081 | snp | A/C/T | 4.96433e-05 | 0.00498192 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408027 | GATGGAGCAGACGGC[A/C/T]GCCAGTCCACAGCAG | 267 |
| rs759989447 | snp | A/G | 1.7268e-05 | 0.00293832 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362893 | GCAGGAGGCAGCTGA[A/G]GAAGGCAAGGGAGCG | 267 |
| rs760069234 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372586 | TACTCAGCTCCCCAC[C/T]CTAGCCTGTTCTTTC | 267 |
| rs760101716 | snp | A/C | 2.78664e-05 | 0.00373262 | intron-variant | AMFR | GRCh38.p7 | 16:56386060 | GTAAGTTTCAGAGCC[A/C]TGACTCTTTCCCCCG | 267 |
| rs760155653 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56398174 | AACTCTATCATTTAT[-/A]ATATATAACTCTATC | 267 |
| rs760199296 | snp | A/C | 0.000201336 | 0.0100313 | missense | AMFR | GRCh38.p7 | 16:56362995 | GGTCAGAGGACGCAC[A/C]TTCCGAGGGGAGGAA | 267 |
| rs760289205 | snp | A/T | 1.65685e-05 | 0.00287819 | missense | AMFR | GRCh38.p7 | 16:56409431 | AAACTCACATATTCA[A/T]ATCGATCCTTGCAGA | 267 |
| rs760303996 | in-del | -/AG | 1.77621e-05 | 0.00298006 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362743 | TAGAAAGTATTACAA[-/AG]AAGGATTAAATTTAT | 267 |
| rs760350312 | snp | A/T | 1.81102e-05 | 0.00300911 | intron-variant | AMFR | GRCh38.p7 | 16:56389420 | AGCATCCTTGATTGT[A/T]CCTTAGCATACTTTG | 267 |
| rs760357423 | in-del | -/G | 1.65482e-05 | 0.00287643 | intron-variant | AMFR | GRCh38.p7 | 16:56405093 | GTTACTACTGAATTT[-/G]GTTTAACCATGTTGT | 267 |
| rs760389261 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56369638 | ATTTTAACTACCATT[C/T]GAACCAGCAATCCCA | 267 |
| rs760407831 | in-del | -/AG | | | intron-variant | AMFR | GRCh38.p7 | 16:56384824 | TTTTTTTTTTGAGAC[-/AG]AGTTTCACTCTTGTT | 267 |
| rs760408487 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377119 | GGGATACTTCCTAAT[A/T]CATACTATAAGGTCA | 267 |
| rs760448090 | snp | C/G | 1.64822e-05 | 0.00287068 | missense | AMFR | GRCh38.p7 | 16:56389242 | TCCCTTCGGCTGCTG[C/G]TACAGGAACCAAATT | 267 |
| rs760507535 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56414384 | GTTTATTTCTTCCTG[A/C]TGAAAAATAAAAGCA | 267 |
| rs760529496 | snp | G/T | 1.77046e-05 | 0.00297523 | missense | AMFR | GRCh38.p7 | 16:56364104 | AGTGGCACACGCTCG[G/T]TCTGGACACGGGGCA | 267 |
| rs760549594 | in-del | -/AC | | | intron-variant | AMFR | GRCh38.p7 | 16:56365595 | TGTAGGTACATACAC[-/AC]ACACACGCACACACA | 267 |
| rs760561443 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56364561 | CTCTGAAAACAGAGG[A/T]AAAAAGGAAAACTGC | 267 |
| rs760582271 | snp | A/G | 8.9191e-05 | 0.00667739 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362487 | CAGATGTTACCCCAC[A/G]ACGTGGGGGCGGGCT | 267 |
| rs760641374 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56377920 | ATGAGGAAAATTACA[A/G]AATCTTGATAAATGA | 267 |
| rs760677206 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56401340 | GGCTTCTTTTGGGCA[G/T]GTACAAAATGCAAAA | 267 |
| rs760742820 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415613 | CAAGGAAGTATGTAA[C/T]ACATTTTTAAAGGAT | 267 |
| rs760743134 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383071 | CTACTGCTCTGTGTC[C/T]TTCTTCATAACATAC | 267 |
| rs760771342 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402104 | GCACTTTCGGAGGCC[A/G]AGGTAGGGGGATCAT | 267 |
| rs760830003 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383870 | GAAGCAAAATCATTC[C/T]GTTAAATATCCTGTC | 267 |
| rs760866634 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422581 | CACTGTCCTCCCCAC[A/G]CCAGACCGAGCTCCA | 267 |
| rs760906789 | snp | A/C | 6.58946e-05 | 0.0057396 | missense | AMFR | GRCh38.p7 | 16:56402989 | TGCTTCCTTACCTGG[A/C]CTCCATGTTTCCAAC | 267 |
| rs761011245 | snp | G/T | 3.3151e-05 | 0.00407117 | intron-variant | AMFR | GRCh38.p7 | 16:56405168 | AATCAACTGTATGAG[G/T]AGGCCTCCATCACCT | 267 |
| rs761015771 | snp | C/T | 1.73084e-05 | 0.00294175 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362889 | GGGCGCAGGAGGCAG[C/T]TGAGGAAGGCAAGGG | 267 |
| rs761031202 | snp | C/T | 0.000295639 | 0.0121545 | missense, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425234 | TGAGCGCGCGGTAGG[C/T]GCTGATGATGGTGCC | 267 |
| rs761033918 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56423492 | TTAGAATCTGAACAT[A/G]GCTTTTATCAAAATA | 267 |
| rs761050843 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56411718 | CTATCCATCAAAAGG[A/G]CAGAGACACCCTAGT | 267 |
| rs761117811 | snp | C/T | 3.38782e-05 | 0.00411557 | missense | AMFR | GRCh38.p7 | 16:56385954 | TGCTGGCCTGCGTAA[C/T]GCCAAGAATGTTGGT | 267 |
| rs761149855 | snp | A/G | 1.78713e-05 | 0.00298921 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362238 | GCACCAGAGTTCACG[A/G]AAATCAAGCCGGCTT | 267 |
| rs761165730 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388132 | GGTGATTTCATTGTT[G/T]TGCGAACATCATAGA | 267 |
| rs761172267 | snp | A/C | | | missense | AMFR | GRCh38.p7 | 16:56364023 | GCCTCGAAGTCTTCC[A/C]CCTCACTGGGCTCCA | 267 |
| rs761176885 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56400930 | AGCACTCAGCACATT[-/A]AAAAAAAAAAAAAAA | 267 |
| rs761186274 | in-del | -/C | 1.71631e-05 | 0.00292938 | frameshift-variant | AMFR | GRCh38.p7 | 16:56405241 | CACTGTCACAAGAAG[-/C]AGACTATAAAAAAGG | 267 |
| rs761252402 | in-del | -/CACT | | | intron-variant | AMFR | GRCh38.p7 | 16:56384735 | ACACACACACACACA[-/CACT]CAATTTTTGGAGGTG | 267 |
| rs761262070 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379246 | ATCTTACATGGATGG[C/T]GGCAGGCAAAGAGAG | 267 |
| rs761293987 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390797 | CTTTTTATAAGCAAA[A/T]CTAAATTTATTTCAC | 267 |
| rs761320091 | snp | C/T | 3.29451e-05 | 0.00405851 | missense | AMFR | GRCh38.p7 | 16:56367479 | CTTCCTGGTCACTGC[C/T]TGGCCTTTCCACAGG | 267 |
| rs761455536 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378902 | ACACCACTACATATA[C/T]ATTAGAATAGCCAAA | 267 |
| rs761464113 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416611 | CTACCACACTAATTT[C/T]TGAATTTTTTTATAG | 267 |
| rs761497043 | snp | A/C | 0.000206292 | 0.010154 | synonymous-codon, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425076 | CGCCTCGCTCACCCA[A/C]ACGAAGAGGCTGTCT | 267 |
| rs761520723 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378183 | TTGACACTGCCTGTC[G/T]AAAAGATTTATTACA | 267 |
| rs761521200 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56392520 | AGAGAAGTCCTTAAA[G/T]GACCTGACGGAGCTG | 267 |
| rs761585749 | snp | A/C | 1.65669e-05 | 0.00287805 | missense | AMFR | GRCh38.p7 | 16:56401839 | CTGGAGTTGCAACTG[A/C]AAACCTGTGGAAACA | 267 |
| rs761624970 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395654 | TCACCACTCCTATTC[A/T]ACACAGTGTTGGAAT | 267 |
| rs761654949 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56367007 | TATCTGGAAATCCTG[A/C]GTTTGACAAGTGAGG | 267 |
| rs761694034 | snp | C/G/T | 0.000105588 | 0.00726526 | missense | AMFR | GRCh38.p7 | 16:56364102 | CCAGTGGCACACGCT[C/G/T]GGTCTGGACACGGGG | 267 |
| rs761731383 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56422912 | TTATTCTAAACTGTG[C/T]TCTAAAAAGATAAGT | 267 |
| rs761769788 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367743 | AAGTTTGAGAGTCAG[C/T]AACTGGTCCCACTTT | 267 |
| rs761782040 | snp | G/T | 1.64741e-05 | 0.00286998 | intron-variant | AMFR | GRCh38.p7 | 16:56402972 | TAGGCAACATCAACT[G/T]GTGCTTCCTTACCTG | 267 |
| rs761815566 | snp | A/C | 1.65274e-05 | 0.00287462 | missense | AMFR | GRCh38.p7 | 16:56369327 | CTTGAATCTGATGAG[A/C]CTACAGGAATACAAA | 267 |
| rs761840656 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56384152 | TCCATCTCATCCTTC[A/G]TGTTTTAGCTTACAT | 267 |
| rs761841277 | snp | C/T | | | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423733 | AGTTGAGTTCTTTCG[C/T]TTCTCCCTTCTTTAG | 267 |
| rs761843259 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56411807 | CGTGAACTAGGAATC[A/G]TTGGTGAAATGTCTG | 267 |
| rs761858107 | in-del | -/GGGACAGGCCTCCTCCAGTCAGTCG | 7.01262e-05 | 0.005921 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362842 | GGAGCGGGCAGAATT[-/GGGACAGGCCTCCTCCAGTCAGTCG]GGGACAGGCCTCCTC | 267 |
| rs761894003 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402197 | AAAAATTAGCCGGGC[A/G]TGGTGACAGGCGCCT | 267 |
| rs761919954 | snp | C/G | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362132 | AAACCATAAACCAAA[C/G]CTTGCTGCCTAACCA | 267 |
| rs761928338 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56391171 | CTCAACCCGAGGCAG[A/G]TAAGTGTTTTAAAAT | 267 |
| rs761930447 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385805 | CCCTAAAAATCCTTC[C/T]ACTCTGCCAGAGCAG | 267 |
| rs762027541 | snp | G/T | 1.65203e-05 | 0.002874 | synonymous-codon | AMFR | GRCh38.p7 | 16:56414269 | GTCTCTCACTCACTC[G/T]AAGAGGGCCAAACAC | 267 |
| rs762069947 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56411894 | GTTTTGAATGACACT[A/G]CCACTTGGCTCTGCC | 267 |
| rs762102510 | snp | A/C | 1.76711e-05 | 0.00297241 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362803 | GCTTTATACAGCGGC[A/C]ATGCAGTCAAGCCCG | 267 |
| rs762158280 | snp | C/T | 3.49266e-05 | 0.00417876 | missense | AMFR | GRCh38.p7 | 16:56385926 | GACCTTACCATTGCA[C/T]TGAGCTGGGAGTTGC | 267 |
| rs762189916 | snp | C/T | 1.65737e-05 | 0.00287864 | intron-variant | AMFR | GRCh38.p7 | 16:56405155 | TGCTACATCTTAAAA[C/T]CAACTGTATGAGTAG | 267 |
| rs762194044 | snp | C/T | 1.78992e-05 | 0.00299153 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362234 | AGGAGCACCAGAGTT[C/T]ACGGAAATCAAGCCG | 267 |
| rs762194372 | snp | A/T | 1.77599e-05 | 0.00297987 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362719 | TCTAAGGGGAAGAGA[A/T]ATGTCACATAGAAAG | 267 |
| rs762197886 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56380824 | TCCATATCATTATCA[A/G]TATTTTGGTTAAAGC | 267 |
| rs762269918 | snp | A/T | 7.23912e-05 | 0.00601584 | intron-variant | AMFR | GRCh38.p7 | 16:56363085 | AAGACTTTTTCTCTC[A/T]CATAGGAGAGATGGG | 267 |
| rs762380239 | snp | A/T | | | missense | AMFR | GRCh38.p7 | 16:56369323 | ATCTCTTGAATCTGA[A/T]GAGCCTACAGGAATA | 267 |
| rs762395972 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56373421 | CCAGAGCATGGGCTC[-/A]ACTAAAAGACGGAGC | 267 |
| rs762438311 | snp | A/C | 5.93807e-05 | 0.00544856 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362152 | CTGCCTAACCACTCC[A/C]CAGGTCCAGACGGGA | 267 |
| rs762476827 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56376062 | GGCTCTGTCTCCAAA[A/G]CATAAATAAATTAAA | 267 |
| rs762482818 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390408 | ATGTGTAGATATAAA[A/G]TTATAAAGGAAAACC | 267 |
| rs762496132 | snp | C/T | 1.77363e-05 | 0.00297789 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362338 | TAGCCCTGGACTTTC[C/T]CCTCCTCTGCTCCAG | 267 |
| rs762500304 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56400019 | CAACCTGCATAACTA[A/G]AGAAACGCTGGTACC | 267 |
| rs762540065 | snp | C/G | 1.65455e-05 | 0.00287619 | missense | AMFR | GRCh38.p7 | 16:56364010 | GCGGCTCCCACGAGC[C/G]TCGAAGTCTTCCACC | 267 |
| rs762710661 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56369067 | GGAAAGTTAGAGAGT[G/T]TATAGAAACCCTTCA | 267 |
| rs762746113 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417732 | TTTCATGTTTACATT[C/T]GGGTCCCATCCCCAA | 267 |
| rs762776771 | snp | G/T | 0.000136505 | 0.00826037 | missense | AMFR | GRCh38.p7 | 16:56362925 | TAGGAGGTCTGCTGC[G/T]TCTGAAGCCTCCGTT | 267 |
| rs762797072 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56389967 | CAGGTCCTTACCTCC[C/T]TGTTCCCCTGGCTCA | 267 |
| rs762843736 | snp | C/G/T | 1.84337e-05 | 0.00303587 | synonymous-codon | AMFR | GRCh38.p7 | 16:56386009 | ACTCGGCAGCCAGCT[C/G/T]GCAATCCGAGACCCT | 267 |
| rs762850802 | snp | A/G | 7.10202e-05 | 0.00595861 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362710 | TGCAGTGTTTCTAAG[A/G]GGAAGAGAAATGTCA | 267 |
| rs762853925 | snp | A/G | | | intron-variant, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56423859 | TAATCTACAGCCCAC[A/G]GAGTCCATAAATCCC | 267 |
| rs762926660 | snp | G/T | 3.31044e-05 | 0.0040683 | missense | AMFR | GRCh38.p7 | 16:56414254 | AGTGTAGACTTACCT[G/T]TCTCTCACTCACTCG | 267 |
| rs762929684 | snp | A/G | 4.95086e-05 | 0.00497512 | missense | AMFR | GRCh38.p7 | 16:56404985 | GTGTAATAGACATAC[A/G]TCCCCTTTCCTTCCC | 267 |
| rs762970734 | in-del | -/CGTCT | 1.74127e-05 | 0.0029506 | intron-variant | AMFR | GRCh38.p7 | 16:56405250 | AAGAAGAGACTATAA[-/CGTCT]AAAAGGATATTTTCT | 267 |
| rs762978772 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56374242 | ACTGTGGGACAACTA[C/T]AAAAGGTGTAAACGC | 267 |
| rs762995273 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56397854 | ATTTATAATATATAA[A/C]TGTATCATTTATAAT | 267 |
| rs763037282 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56412969 | ATACAAAATAGTCCT[C/G]TTCACAATGGCATCC | 267 |
| rs763053426 | snp | C/G | 2.23366e-05 | 0.00334183 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362111 | ATTTACTTCACCAAT[C/G]AATGAAAACCATAAA | 267 |
| rs763068693 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375312 | AGTAACAAGTATACT[A/G]ATATGCTAAGAAAGG | 267 |
| rs763096167 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426076 | AATGGTGCAGCTGTC[C/T]TGGAAAATAACCTGT | 267 |
| rs763145862 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379974 | TCTGGAGGACAGTGG[C/T]CCTCTTCTCATAGCT | 267 |
| rs763214771 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56396081 | ATGGATAGGAAGAAT[C/G]AATATCGTGAAAATG | 267 |
| rs763219003 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369319 | AAACATCTCTTGAAT[C/T]TGATGAGCCTACAGG | 267 |
| rs763222767 | snp | A/T | 3.54799e-05 | 0.00421173 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362584 | ACGTACGCATGAGGC[A/T]GGAGTAGAAGCTGCC | 267 |
| rs763234592 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56381388 | ACTTACGTCTACATA[A/G]AAACCTGCACATAAA | 267 |
| rs763245519 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56392215 | AAAACCCCATCTGTA[C/T]GTCACCATCATCAAA | 267 |
| rs763250321 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56367184 | GTGGCAGGGCTGGCC[A/C]CGGGGAACACAACCC | 267 |
| rs763269973 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56374400 | AAGCAGGACAAAGGT[-/A]AAAAAAAAAAAAAAA | 267 |
| rs763278523 | snp | C/T | 1.65452e-05 | 0.00287616 | intron-variant | AMFR | GRCh38.p7 | 16:56405069 | GAGAAAACACCTTAG[C/T]AATTTACTGTTACTA | 267 |
| rs763337546 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56371517 | GACCCCAAAGAACCC[A/C]TGTAATGCCTGCCAT | 267 |
| rs763349779 | snp | C/T | 1.88884e-05 | 0.00307309 | missense | AMFR | GRCh38.p7 | 16:56363054 | CTTTTGTTCAAGAAA[C/T]GTCTAGAAAAAACAG | 267 |
| rs763379269 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56406219 | TTTTTTTTTTTTTTT[-/G]TAGAGACAAGGTCTT | 267 |
| rs763484736 | snp | C/G | 1.7809e-05 | 0.00298398 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362255 | AATCAAGCCGGCTTT[C/G]GACTGGAGGCTCGGA | 267 |
| rs763502701 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56409616 | AATGTTTATGAAGGT[A/G]AGTACCATCACACCT | 267 |
| rs763570636 | snp | C/T | 1.65493e-05 | 0.00287652 | missense | AMFR | GRCh38.p7 | 16:56364012 | GGCTCCCACGAGCCT[C/T]GAAGTCTTCCACCTC | 267 |
| rs763598020 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402511 | ATCTTGCACCTCCAG[A/G]CGTGGCTTAGCCCCA | 267 |
| rs763658354 | in-del | -/T | 1.77288e-05 | 0.00297726 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362776 | GCTGTCCAAACACTA[-/T]TAAGACCACATGCTT | 267 |
| rs763795086 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375779 | AAGTATATACACCTG[C/T]TGGGCACAGTGGCTC | 267 |
| rs763812198 | snp | A/G | 6.61857e-05 | 0.00575226 | intron-variant | AMFR | GRCh38.p7 | 16:56407941 | AAATACAATCTGAGC[A/G]AGTCCTGCATCCAGT | 267 |
| rs763827808 | snp | C/T | 1.65485e-05 | 0.00287645 | missense | AMFR | GRCh38.p7 | 16:56414256 | TGTAGACTTACCTGT[C/T]TCTCACTCACTCGAA | 267 |
| rs763828151 | snp | A/T | 1.65485e-05 | 0.00287645 | intron-variant | AMFR | GRCh38.p7 | 16:56401704 | TGGACAGAACACCTG[A/T]CCCACATGGCCCTTC | 267 |
| rs763834426 | snp | C/T | 0.000124194 | 0.00787918 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362348 | CTTTCCCCTCCTCTG[C/T]TCCAGGTATCGAACC | 267 |
| rs763916056 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | AMFR | GRCh38.p7 | 16:56409517 | CACCTCTTCCACTGT[C/T]TGGACATTCAGCACA | 267 |
| rs763951839 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390112 | GCCTTAATTATGGTA[A/G]ACATTCAATAAATAC | 267 |
| rs763976405 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56400058 | TCCTCACTTTCCCTC[A/G]GCCGGTCTGGCATCA | 267 |
| rs764024142 | snp | G/T | 4.96192e-05 | 0.00498067 | missense | AMFR | GRCh38.p7 | 16:56401818 | CATTGTTGACAGCCA[G/T]CTCCTCTGGAGTTGC | 267 |
| rs764027760 | in-del | -/AT | | | intron-variant | AMFR | GRCh38.p7 | 16:56365950 | CCATTATATATACAT[-/AT]ATATATATATAAAAT | 267 |
| rs764062585 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56371885 | GTCATTATTCCTAAA[C/T]AATACAGTGTATAAC | 267 |
| rs764100167 | snp | C/T | 1.67663e-05 | 0.00289532 | intron-variant | AMFR | GRCh38.p7 | 16:56363913 | GGTGGTCTGGAGAAG[C/T]GACTCACTTGCGAGC | 267 |
| rs764155747 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56422669 | TCCAAGCTGGTTCAA[A/C]CACCACCTTCCATGA | 267 |
| rs764177299 | in-del | -/A | 5.07112e-05 | 0.00503518 | intron-variant | AMFR | GRCh38.p7 | 16:56409401 | GGTGACTAAGCAAGC[-/A]AAAAGCTTGGCTAAA | 267 |
| rs764241536 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423583 | GTTCCTTCTCAAAGG[C/T]TTATTTATATCTTAG | 267 |
| rs764248023 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56369181 | TATCATGCTTTAAAA[A/G]CCCAGTTTTACCTGT | 267 |
| rs764320105 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56410815 | TGAACCTGGGAGGTC[A/G]AGGTTGCAGGGAGCC | 267 |
| rs764338868 | snp | C/T | 1.6777e-05 | 0.00289624 | synonymous-codon | AMFR | GRCh38.p7 | 16:56362990 | CACGGGGTCAGAGGA[C/T]GCACCTTCCGAGGGG | 267 |
| rs764354351 | snp | A/G | 1.77587e-05 | 0.00297977 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362717 | TTTCTAAGGGGAAGA[A/G]AAATGTCACATAGAA | 267 |
| rs764396324 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411727 | AAAAGGGCAGAGACA[C/T]CCTAGTGGTAATGAG | 267 |
| rs764444677 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56372912 | AATTGCTTGAACCTG[A/G]GAGGTGGAGGTTGCA | 267 |
| rs764446255 | in-del | -/CAAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56399339 | GTGAGAACAAGTCCT[-/CAAA]CAGATACTTCTTACA | 267 |
| rs764446288 | snp | C/T | 1.6504e-05 | 0.00287258 | missense | AMFR | GRCh38.p7 | 16:56369320 | AACATCTCTTGAATC[C/T]GATGAGCCTACAGGA | 267 |
| rs764446412 | snp | A/G | 1.77404e-05 | 0.00297824 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362585 | CGTACGCATGAGGCA[A/G]GAGTAGAAGCTGCCT | 267 |
| rs764451640 | in-del | -/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56380583 | CTTTTAAAACTGAAT[-/G]CCTTTAACAGCATCC | 267 |
| rs764461507 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56417001 | CTACAAAGGATTGAA[A/C]GCAATCCTTATTTTA | 267 |
| rs764470756 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56392302 | AATTCTAAAAATCAG[A/C]GTGCCTCTCCTCCTC | 267 |
| rs764581795 | snp | G/T | 1.7117e-05 | 0.00292544 | missense | AMFR | GRCh38.p7 | 16:56362917 | GGGAGCGCTAGGAGG[G/T]CTGCTGCTTCTGAAG | 267 |
| rs764613831 | snp | C/G | 1.64925e-05 | 0.00287158 | missense | AMFR | GRCh38.p7 | 16:56389235 | CGAGGTCTCCCTTCG[C/G]CTGCTGCTACAGGAA | 267 |
| rs764617193 | snp | A/G | 1.74069e-05 | 0.00295011 | intron-variant | AMFR | GRCh38.p7 | 16:56389166 | TTAGGTATAGTTTCA[A/G]AGGTTGAAACCAACT | 267 |
| rs764652331 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56409847 | TTAGCTATTCAAAGG[A/G]TAGCGATATTAGTTT | 267 |
| rs764736879 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415717 | GCCCAAACTAGTTGC[C/T]CCAAATATCCTAATC | 267 |
| rs764757053 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379272 | GAGAGAGAGCTTGTG[C/T]AGGTGAACTCCTCTT | 267 |
| rs764808221 | snp | C/G | 1.69178e-05 | 0.00290837 | intron-variant | AMFR | GRCh38.p7 | 16:56363898 | ATCTGGATTATGCCA[C/G]GTGGTCTGGAGAAGC | 267 |
| rs764853494 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378222 | GTAATCAAGACAATG[C/T]GGTATTGGCAAAAGA | 267 |
| rs764892916 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56397329 | GTGGCACATATATAC[C/T]ATGGAATACCATGCA | 267 |
| rs764912503 | snp | C/T | 1.78452e-05 | 0.00298702 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362247 | TTCACGGAAATCAAG[C/T]CGGCTTTGGACTGGA | 267 |
| rs764926190 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56365054 | GCCAGGGTCAGCCCA[C/T]TGCCCGCTTCTAGGC | 267 |
| rs764962608 | snp | A/C/T | 8.27446e-05 | 0.00643169 | missense | AMFR | GRCh38.p7 | 16:56364005 | GAGAAGCGGCTCCCA[A/C/T]GAGCCTCGAAGTCTT | 267 |
| rs764967834 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56401506 | CCATACCCAGAAACT[A/G]AGATGGCAAACTATG | 267 |
| rs765000209 | snp | A/G | 1.90842e-05 | 0.00308897 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362164 | TCCCCAGGTCCAGAC[A/G]GGACAAGGAAATGCT | 267 |
| rs765034044 | in-del | -/T | 1.75799e-05 | 0.00296474 | frameshift-variant | AMFR | GRCh38.p7 | 16:56363039 | CATCATCTTCAGAAC[-/T]TTTTGTTCAAGAAAC | 267 |
| rs765054761 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402243 | CAGGAGGCTGAGGCA[A/G]GAGACTTACTTCAAC | 267 |
| rs765107949 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416655 | CCATGCTGCCCAGGC[A/T]GGTCTCGAACTCCTG | 267 |
| rs765166104 | snp | C/T | 1.64874e-05 | 0.00287113 | stop-gained | AMFR | GRCh38.p7 | 16:56409493 | GGCAAACCAGAGGCA[C/T]CACATGACCACCTCT | 267 |
| rs765184003 | snp | A/G/T | 4.9847e-05 | 0.00499214 | intron-variant | AMFR | GRCh38.p7 | 16:56369178 | ATTTATCATGCTTTA[A/G/T]AAGCCCAGTTTTACC | 267 |
| rs765222433 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | AMFR | GRCh38.p7 | 16:56389288 | TCCTTGATGTTCTTC[C/G]CTGACACGATTATTG | 267 |
| rs765224634 | in-del | -/T | 1.72674e-05 | 0.00293827 | splice-acceptor-variant | AMFR | GRCh38.p7 | 16:56405244 | TGTCACAAGAAGAGA[-/T]CTATAAAAAAGGATA | 267 |
| rs765284910 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56411895 | TTTTGAATGACACTG[A/C]CACTTGGCTCTGCCA | 267 |
| rs765315943 | snp | A/G | 1.78194e-05 | 0.00298486 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362496 | CCCCACGACGTGGGG[A/G]CGGGCTCACACTGTG | 267 |
| rs765408220 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56377080 | TCAATTCTCTACAAT[-/C]TCTTTCAGAGGACAG | 267 |
| rs765477204 | snp | C/T | 6.58979e-05 | 0.00573974 | missense | AMFR | GRCh38.p7 | 16:56403027 | AGATAGTTCTTGTGC[C/T]GACGAATTCGACGTT | 267 |
| rs765497157 | snp | C/G | 1.6537e-05 | 0.00287545 | intron-variant | AMFR | GRCh38.p7 | 16:56386072 | GCCCTGACTCTTTCC[C/G]CCGTCATCTGCTCTC | 267 |
| rs765553064 | snp | G/T | 3.51556e-05 | 0.00419244 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362834 | CTTTTCCATGGAGCG[G/T]GCAGAATTGGGACAG | 267 |
| rs765553200 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416607 | GAGCTACCACACTAA[-/T]TTTTTGAATTTTTTT | 267 |
| rs765561836 | snp | C/T | 0.000160995 | 0.00897058 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362236 | GAGCACCAGAGTTCA[C/T]GGAAATCAAGCCGGC | 267 |
| rs765585471 | snp | A/G | 1.64885e-05 | 0.00287123 | intron-variant | AMFR | GRCh38.p7 | 16:56367531 | GCTATCTGACCGCTG[A/G]AAGAGAAACAGTACC | 267 |
| rs765621235 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386765 | ACACATTTAAGGCTG[C/T]TTTTCATTCCTTCAC | 267 |
| rs765677317 | snp | C/G | 0.000270819 | 0.0116334 | missense, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425309 | GCCAGGGGAAGCGCT[C/G]GAGGAAGAGCAGCGG | 267 |
| rs765736232 | in-del | -/AAAAAAAAAAAAAAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56382510 | GATAGCTGATGAGCT[-/AAAAAAAAAAAAAAA]AAAAAAAAAAGGCAA | 267 |
| rs765829301 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56423365 | TGATAAACCTGCCAG[A/G]GGTAAGACCTCTACT | 267 |
| rs765849433 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56393010 | ATCAGACTAACAGCT[C/G]ATCTCTCAGCAGACA | 267 |
| rs765874411 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416745 | CTGCGCCCAGCCTAA[A/G]TAAGTCTTTGAATTC | 267 |
| rs765875650 | snp | A/G | 1.9615e-05 | 0.00313163 | intron-variant | AMFR | GRCh38.p7 | 16:56408133 | TGAAATGCACACAGT[A/G]GGAAACTGCTCATTC | 267 |
| rs765887156 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56367118 | AGGCACCCTCACGGT[C/T]CCGAGCCCAGCTTCC | 267 |
| rs765945127 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378353 | GCAAAGGCAATACAA[G/T]AGAGAAAAGATAGAC | 267 |
| rs765961894 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | AMFR | GRCh38.p7 | 16:56389245 | CTTCGGCTGCTGCTA[C/T]AGGAACCAAATTCTC | 267 |
| rs766104777 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56384455 | ATCAATAAAGATTAA[C/G]TAATTAACGAATGAA | 267 |
| rs766118689 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372371 | CAGGTTCATTCATGC[C/T]GCAGCATGCAACAGG | 267 |
| rs766159010 | snp | A/G | 1.84742e-05 | 0.0030392 | intron-variant | AMFR | GRCh38.p7 | 16:56389426 | CTTGATTGTTCCTTA[A/G]CATACTTTGTGAGAA | 267 |
| rs766159022 | snp | A/G | 3.35852e-05 | 0.00409774 | missense | AMFR | GRCh38.p7 | 16:56363000 | GAGGACGCACCTTCC[A/G]AGGGGAGGAAGCTCT | 267 |
| rs766164120 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386098 | CTCTCACGGTAGCCA[C/T]TGTAATGGCTGGTGT | 267 |
| rs766192767 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380128 | ATCCAGGTGTTTCCA[C/T]ACATCTTCTGAAATC | 267 |
| rs766252601 | snp | C/T | 1.72841e-05 | 0.00293969 | intron-variant | AMFR | GRCh38.p7 | 16:56403154 | AACACACGGTAAAAG[C/T]GAACGTGAACTTGCT | 267 |
| rs766277340 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411998 | TCTTATAATAACAGC[A/T]TATACCTCATAGAAT | 267 |
| rs766344144 | in-del | -/CATACC | 1.7475e-05 | 0.00295588 | intron-variant | AMFR | GRCh38.p7 | 16:56405252 | GAAGAGACTATAAAA[-/CATACC]AAGGATATTTTCTTT | 267 |
| rs766364042 | snp | C/T | 1.72898e-05 | 0.00294017 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362890 | GGCGCAGGAGGCAGC[C/T]GAGGAAGGCAAGGGA | 267 |
| rs766482198 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374250 | ACAACTACAAAAGGT[A/G]TAAACGCACTTAATG | 267 |
| rs766511582 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | AMFR | GRCh38.p7 | 16:56403009 | ATGTTTCCAACCACA[C/T]GTAGATAGTTCTTGT | 267 |
| rs766513051 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363319 | CACAGAACTCCCACA[A/G]TCACAGGGTCTGCCA | 267 |
| rs766522805 | snp | C/T | 0.000286903 | 0.0119737 | missense, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425236 | AGCGCGCGGTAGGCG[C/T]TGATGATGGTGCCCA | 267 |
| rs766527862 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380020 | CTAGCAGGCATTCTG[C/T]GTAGGGGCTCTGATC | 267 |
| rs766570254 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375482 | ATAATCACTTTGAAC[A/G]TCAATGGCCTAAATG | 267 |
| rs766571337 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56414829 | GGGGTAGGAGTGTGG[A/G]TGGTCACAAAAAAGT | 267 |
| rs766602701 | snp | A/C | 1.65023e-05 | 0.00287244 | missense | AMFR | GRCh38.p7 | 16:56414298 | ACAATACACTGGATG[A/C]GCTTAGCCACCAACA | 267 |
| rs766630194 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370497 | GGGTGCGGATCAAAC[C/T]GTTGTACATCTTGTT | 267 |
| rs766703557 | snp | C/T | 9.97738e-05 | 0.00706236 | intron-variant | AMFR | GRCh38.p7 | 16:56369351 | ATACAAATACAGAGT[C/T]CACAGAAACGTTCAC | 267 |
| rs766705536 | snp | A/G | 1.93171e-05 | 0.00310776 | intron-variant | AMFR | GRCh38.p7 | 16:56405291 | ATGTAGCATTGCTCA[A/G]GCCAAACTTTTTATA | 267 |
| rs766734473 | in-del | -/CAAAAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56401131 | AAGGTCCATCAACAT[-/CAAAAC]ACCAAACCTATACAC | 267 |
| rs766793327 | snp | A/G | 1.6577e-05 | 0.00287893 | intron-variant | AMFR | GRCh38.p7 | 16:56405169 | ATCAACTGTATGAGT[A/G]GGCCTCCATCACCTC | 267 |
| rs766834662 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56420886 | CACTTAATTTGCATA[A/G]TTAAGTCAGAACCTT | 267 |
| rs766847539 | snp | C/T | 0.000123323 | 0.00785152 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362827 | AAGCCCGCTTTTCCA[C/T]GGAGCGGGCAGAATT | 267 |
| rs766887950 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419383 | TAAAATTTTTTTAAA[G/T]TTTAGAATCTACTAA | 267 |
| rs766901764 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | AMFR | GRCh38.p7 | 16:56385955 | GCTGGCCTGCGTAAT[A/G]CCAAGAATGTTGGTG | 267 |
| rs766922511 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56409013 | ATTCAGTCCTGGCCC[A/G]GGGTGGAAATAGTAT | 267 |
| rs767008064 | snp | C/T | 1.78497e-05 | 0.00298739 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362484 | TAACAGATGTTACCC[C/T]ACGACGTGGGGGCGG | 267 |
| rs767084338 | snp | C/G | 1.65649e-05 | 0.00287788 | missense | AMFR | GRCh38.p7 | 16:56408037 | ACGGCCGCCAGTCCA[C/G]AGCAGGAAAGCAGCA | 267 |
| rs767096866 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417864 | ATACTGAAAGAAACA[C/T]AACTGGAGCATTCCT | 267 |
| rs767143282 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56368026 | GTATTTCATTGCCTG[A/T]GGACTTTCTCTGGCT | 267 |
| rs767207219 | snp | A/G | 0.000194269 | 0.00985377 | intron-variant, missense | AMFR | GRCh38.p7 | 16:56388766 | AGCCTACACAGGTCA[A/G]GAGCATCAGTATCAC | 267 |
| rs767244594 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374620 | AAAAGACTCACCAAC[A/G]GAGAATTCTATACCC | 267 |
| rs767281747 | snp | C/T | 1.656e-05 | 0.00287745 | missense | AMFR | GRCh38.p7 | 16:56364021 | GAGCCTCGAAGTCTT[C/T]CACCTCACTGGGCTC | 267 |
| rs767323826 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56375561 | ACTGAATGTTGTTTA[A/C]CCACTTTAAAATAAA | 267 |
| rs767325734 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | AMFR | GRCh38.p7 | 16:56402977 | AACATCAACTTGTGC[C/T]TCCTTACCTGGCCTC | 267 |
| rs767386077 | snp | A/G | 0.000106487 | 0.00729603 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362359 | TCTGCTCCAGGTATC[A/G]AACCAAGAGTTCCTT | 267 |
| rs767433990 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56392738 | CAAATCTATGTCTGA[C/T]TGGTGTACCTGAAAG | 267 |
| rs767443433 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421076 | GCTGACTCTTATTTT[A/T]AAAAGCCTATTTTCA | 267 |
| rs767463408 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56381725 | GGCAGAGTGCATACA[A/G]AATCTTTAGGGCAGT | 267 |
| rs767507090 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413979 | GTAAAAATGCCTTTG[C/T]TCTTAGAAAATACAA | 267 |
| rs767512226 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56364482 | CTGTTCACTTCTACT[A/G]ATTGCTCAAACATTT | 267 |
| rs767514536 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399688 | ACTATGGGGCACTAT[C/T]GTGGAGTGATAAAAA | 267 |
| rs767560937 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363487 | GTACAATGCTCAGCT[A/G]AAAGGCAGAGTGGTC | 267 |
| rs767603580 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56401335 | CTTAAGGCTTCTTTT[A/G]GGCATGTACAAAATG | 267 |
| rs767605756 | snp | C/T | 1.77603e-05 | 0.0029799 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362721 | TAAGGGGAAGAGAAA[C/T]GTCACATAGAAAGTA | 267 |
| rs767653584 | snp | A/G | 1.76468e-05 | 0.00297037 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362813 | GCGGCAATGCAGTCA[A/G]GCCCGCTTTTCCATG | 267 |
| rs767697771 | snp | A/C | 1.65726e-05 | 0.00287855 | intron-variant | AMFR | GRCh38.p7 | 16:56369339 | GAGCCTACAGGAATA[A/C]AAATACAGAGTCCAC | 267 |
| rs767760738 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56414031 | GGGTAATGATGTCCA[-/C]CAACTTACTCTCAAA | 267 |
| rs767768093 | snp | A/C/G | 3.84071e-05 | 0.00438205 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362162 | ACTCCCCAGGTCCAG[A/C/G]CGGGACAAGGAAATG | 267 |
| rs767812780 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56422366 | ATGCCAGAGGTCCAC[A/C]TTTTGAGAAAGAAAC | 267 |
| rs767986187 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388368 | TGCATAGGGCACTTA[C/T]CAGGAATGAAGCTTG | 267 |
| rs768020438 | snp | C/T | 3.3157e-05 | 0.00407154 | intron-variant | AMFR | GRCh38.p7 | 16:56405156 | GCTACATCTTAAAAT[C/T]AACTGTATGAGTAGG | 267 |
| rs768026126 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56408725 | AAATGAGGGTTGAAT[C/G]TGAAAGAAATAAAGG | 267 |
| rs768037225 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409172 | ACAAAACAGTCTGCA[C/T]AGGTGAAGTGACCCC | 267 |
| rs768075244 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383536 | ACCCAAATAGAACAC[C/T]GCGACCCATCCTCAT | 267 |
| rs768078060 | snp | A/G | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56389363 | TTGTTCTAGCCAGGA[A/G]CGAAGACAGGAGCTA | 267 |
| rs768109155 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374414 | AAAAAAAAAAAAAAA[-/C]AAAAAAAAACACTAC | 267 |
| rs768126600 | snp | A/C | 1.65064e-05 | 0.00287279 | missense | AMFR | GRCh38.p7 | 16:56403091 | AGATGACCAGGCTGG[A/C]CATGGATAACCAGAT | 267 |
| rs768128041 | snp | C/T | 1.78704e-05 | 0.00298913 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362461 | CCACAACAACGACAG[C/T]AGTTTGATAACAGAT | 267 |
| rs768168824 | in-del | -/TAGATCACTG | 1.69931e-05 | 0.00291483 | frameshift-variant | AMFR | GRCh38.p7 | 16:56405235 | AGTCCTCACTGTCAC[-/TAGATCACTG]AAGAAGAGACTATAA | 267 |
| rs768293820 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56420357 | TTAAGGACAATTCAC[C/G]TATTGTTACCTCTCT | 267 |
| rs768309021 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56420696 | CTAAAACCTAGGAAG[A/T]CACTTTCAGCTCTTA | 267 |
| rs768334761 | snp | A/C | 2.18072e-05 | 0.00330198 | intron-variant | AMFR | GRCh38.p7 | 16:56386038 | CTGAAACAAACAAGA[A/C]TCCAGTGTAAGTTTC | 267 |
| rs768394386 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378019 | AGATGTCCATTCTTC[C/T]CAACTTGATGTACAG | 267 |
| rs768395114 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56372385 | CTGCAGCATGCAACA[C/G]GATTCCCTTCCTTTT | 267 |
| rs768417928 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56410214 | TTTTAATGCACAATG[A/G]AAAAGAATGGCAAGG | 267 |
| rs768527670 | snp | C/G | | | missense | AMFR | GRCh38.p7 | 16:56408059 | AAAGCAGCATGGCAA[C/G]CAACAGGGACAGGAC | 267 |
| rs768568190 | snp | A/G | 1.76877e-05 | 0.00297381 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362797 | CCACATGCTTTATAC[A/G]GCGGCAATGCAGTCA | 267 |
| rs768584699 | snp | C/T | 3.39749e-05 | 0.00412144 | intron-variant | AMFR | GRCh38.p7 | 16:56414392 | CTTCCTGCTGAAAAA[C/T]AAAAGCAGCTCTAAA | 267 |
| rs768598355 | snp | C/T | 3.30863e-05 | 0.00406719 | intron-variant | AMFR | GRCh38.p7 | 16:56405072 | AAAACACCTTAGTAA[C/T]TTACTGTTACTACTG | 267 |
| rs768600503 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56406432 | AAAATTAGCCAGGCA[C/T]GGTGGTTCATGCCTG | 267 |
| rs768602498 | snp | A/G | 1.79738e-05 | 0.00299776 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362221 | ACTCATGAGATGCAG[A/G]AGCACCAGAGTTCAC | 267 |
| rs768644320 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56378901 | GACACCACTACATAT[A/G]TATTAGAATAGCCAA | 267 |
| rs768680941 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368538 | TCATACACAAATTCC[A/G]CGGTCCTGCCAGAAG | 267 |
| rs768734279 | snp | C/T | 9.88989e-05 | 0.00703134 | missense | AMFR | GRCh38.p7 | 16:56367526 | CTGATGCTATCTGAC[C/T]GCTGGAAGAGAAACA | 267 |
| rs768831343 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385620 | CTCCAGAAAAAAAAA[A/T]TTTTTTTTTTTTTGG | 267 |
| rs768876732 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56417475 | TCAGTTAACAAAGGC[C/T]TGAAAAATTGTAAAT | 267 |
| rs768882993 | in-del | -/TAAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56369113 | TATTCAGCTGTTAAG[-/TAAC]TAAAACAGTTAACCT | 267 |
| rs768917016 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373790 | CAGAAACACCAACAC[G/T]AGTGAAGAATTCCCG | 267 |
| rs768957397 | snp | A/G | 6.88314e-05 | 0.00586609 | synonymous-codon | AMFR | GRCh38.p7 | 16:56405242 | CACTGTCACAAGAAG[A/G]GACTATAAAAAAGGA | 267 |
| rs768985676 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427274 | CACTTTGGTTCTCTT[C/T]CCACAGCCATGCAAT | 267 |
| rs769027151 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56375208 | TTAGCTATCATTATT[A/G]TTAGTGTATTTTATG | 267 |
| rs769038909 | snp | A/G | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424672 | TTGAACCTGCCCTCT[A/G]AGATCTTCTAGTTTC | 267 |
| rs769041132 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412603 | AGTGGCTCACACCTA[C/T]AATTCCAGCACTTTG | 267 |
| rs769141548 | snp | C/G | 2.16574e-05 | 0.00329063 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362128 | ATGAAAACCATAAAC[C/G]AAAGCTTGCTGCCTA | 267 |
| rs769160636 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386494 | ACATGAGCTTTGGCT[C/T]CTCTTTCACAAGCTA | 267 |
| rs769197251 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56372427 | ACTATTCTACTGTAC[A/C]GGTTTGCCATATCTT | 267 |
| rs769202162 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363125 | AACACAGCCAGAAGG[G/T]TGATTTCACATCTCC | 267 |
| rs769231179 | snp | C/T | 1.9371e-05 | 0.0031121 | splice-acceptor-variant | AMFR | GRCh38.p7 | 16:56363058 | TGTTCAAGAAACGTC[C/T]AGAAAAAACAGAAGA | 267 |
| rs769271570 | snp | A/C | 1.66219e-05 | 0.00288283 | intron-variant | AMFR | GRCh38.p7 | 16:56414368 | AAATCAGAGAAAGGA[A/C]GTTTATTTCTTCCTG | 267 |
| rs769274825 | snp | A/G | 1.69689e-05 | 0.00291275 | missense | AMFR | GRCh38.p7 | 16:56364075 | GCGTCTCCTCCAGGC[A/G]AGGACTGAGGTCCAG | 267 |
| rs769305833 | snp | A/G | 1.64969e-05 | 0.00287196 | missense | AMFR | GRCh38.p7 | 16:56401766 | CAGGGCAGTTTCCGC[A/G]CAGCCTGCATGGAGT | 267 |
| rs769316964 | snp | C/T | 1.65181e-05 | 0.00287381 | missense | AMFR | GRCh38.p7 | 16:56401800 | AACAGATGGCACAGT[C/T]GTCATTGTTGACAGC | 267 |
| rs769340178 | in-del | -/AAAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56372986 | CAAGACTCGGTGTTA[-/AAAC]AAACAAACAAACAAC | 267 |
| rs769466764 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56417688 | CTTCAGGGTATGTGT[A/C]TGAATGAGATGTATA | 267 |
| rs769479078 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56392022 | GAGACAAAACCTCCA[C/G]AGGAACCATCAGACA | 267 |
| rs769654904 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375975 | AGGGAGGAGAATCGC[C/T]TGAACCCAGGAGGTG | 267 |
| rs769682574 | snp | C/G | 1.67663e-05 | 0.00289532 | missense | AMFR | GRCh38.p7 | 16:56405225 | ATCACATGAGCAGTC[C/G]TCACTGTCACAAGAA | 267 |
| rs769682683 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369304 | GTATGGAACCTGGGG[A/G]AACATCTCTTGAATC | 267 |
| rs769694613 | in-del | -/CCA | | | intron-variant | AMFR | GRCh38.p7 | 16:56412489 | TGGTGCCAGATCAAT[-/CCA]CCACCAAGCCTGCCT | 267 |
| rs769709750 | snp | A/C | 1.77206e-05 | 0.00297657 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362779 | TGTCCAAACACTATA[A/C]GACCACATGCTTTAT | 267 |
| rs769769657 | snp | A/G | 1.65304e-05 | 0.00287488 | intron-variant | AMFR | GRCh38.p7 | 16:56405049 | TTACGTATCTGTAAT[A/G]AAGAGAGAAAACACC | 267 |
| rs769818941 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56393874 | CTAATAGACATCTAC[A/G]GAACTCTCCACCACA | 267 |
| rs769875610 | snp | A/C | 2.11714e-05 | 0.0032535 | intron-variant | AMFR | GRCh38.p7 | 16:56385880 | GTTCTTTCCCTCCTA[A/C]TTCCCAGTGATCTTC | 267 |
| rs769943492 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56405433 | GAAACCCAACTTTTA[C/T]TGAGGAAAAGTCCTG | 267 |
| rs769969830 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56386621 | TTTTTAAATTGTTCT[A/G]TTCTACAAAAAGGCT | 267 |
| rs770033124 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56422206 | CACTCTAGCCTCTTC[A/C]TAGGTCAGTTTTTCA | 267 |
| rs770051170 | snp | C/G | 8.99746e-05 | 0.00670665 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362104 | CTGCCTAATTTACTT[C/G]ACCAATGAATGAAAA | 267 |
| rs770126380 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415175 | CACCTAAACGCCAAA[C/T]CTTAATGCTTACAAA | 267 |
| rs770126534 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399200 | AGAAACTAGACCCCT[C/T]AGGTATTGTTGGGGG | 267 |
| rs770145425 | snp | A/C | 1.69097e-05 | 0.00290768 | intron-variant | AMFR | GRCh38.p7 | 16:56389378 | ACGAAGACAGGAGCT[A/C]CCAAAAAGTCCAAAA | 267 |
| rs770150044 | in-del | -/AAAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56382510 | GATAGCTGATGAGCT[-/AAAA]AAAAAAAAAAAAAAA | 267 |
| rs770163241 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56413703 | TATGCTTTTAGAACA[A/G]TGATTCTTAATTCAC | 267 |
| rs770171181 | snp | C/T | 1.64999e-05 | 0.00287222 | missense | AMFR | GRCh38.p7 | 16:56404982 | TCTGTGTAATAGACA[C/T]ACGTCCCCTTTCCTT | 267 |
| rs770172374 | snp | C/T | 1.77584e-05 | 0.00297974 | missense | AMFR | GRCh38.p7 | 16:56408098 | GGCTGCTCATCGGCG[C/T]GGTGGGCGAGAAGGA | 267 |
| rs770182849 | snp | A/G | 1.77593e-05 | 0.00297982 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362542 | CTTCCCACTGGGTGT[A/G]GTGCTCAGGACACCT | 267 |
| rs770203982 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56375247 | AAGACAATTCTTCTT[C/T]CAATGTGGCCCAGGG | 267 |
| rs770205578 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387541 | TAGCACTACTGCTAA[C/T]AAAATTCCAGGGATG | 267 |
| rs770233294 | snp | C/T | 5.02828e-05 | 0.00501387 | intron-variant | AMFR | GRCh38.p7 | 16:56409412 | AAGCAAAAAGCTTGG[C/T]TAAAAACTCACATAT | 267 |
| rs770361851 | snp | C/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362790 | TATAAGACCACATGC[C/T]TTATACAGCGGCAAT | 267 |
| rs770366707 | snp | C/T | 3.29968e-05 | 0.00406169 | missense | AMFR | GRCh38.p7 | 16:56389233 | AGCGAGGTCTCCCTT[C/T]GGCTGCTGCTACAGG | 267 |
| rs770370591 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56412460 | TTTAGGGAAAAGAAA[G/T]TATATAAAGCCCACT | 267 |
| rs770421431 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383256 | TGTAAGAATTCCACA[C/T]GCTTGACTCTTCCCT | 267 |
| rs770497688 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385269 | CTGTGCCCAGCCTCA[C/T]AAAATTTTTAATAAA | 267 |
| rs770523750 | snp | A/T | 6.24181e-05 | 0.00558616 | intron-variant | AMFR | GRCh38.p7 | 16:56414203 | CATAATACAAAGTTT[A/T]AAAAAAAAAATCTAG | 267 |
| rs770595113 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56370068 | CACTCTTTAGGTGAC[A/G]GTAACACTAAAAGCC | 267 |
| rs770621744 | snp | A/G | 1.74763e-05 | 0.00295598 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362091 | ACAGGCTTTAGCACT[A/G]CCTAATTTACTTCAC | 267 |
| rs770691120 | in-del | -/TA | | | intron-variant | AMFR | GRCh38.p7 | 16:56399082 | CTTAAGAATTATTAC[-/TA]AAAAAAAAAACAAAA | 267 |
| rs770719189 | in-del | -/CC | | | intron-variant | AMFR | GRCh38.p7 | 16:56365593 | CATGTAGGTACATAC[-/CC]ACACACACGCACACA | 267 |
| rs770744053 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56418611 | TCAGGAGATCGAGAC[C/T]ATCCTGGTTAACTCA | 267 |
| rs770775751 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56369084 | ATAGAAACCCTTCAT[G/T]AAGTCATAAATGATA | 267 |
| rs770784743 | snp | A/G | 1.77517e-05 | 0.00297919 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362569 | ACCTGCATTTGTGGG[A/G]CGTACGCATGAGGCA | 267 |
| rs770832855 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369264 | CAACTGAGCGTGTCA[A/G]CTGGAGGTCCTGCAG | 267 |
| rs770862376 | snp | C/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426616 | TCTCTCCAGTAGCTG[C/G]GATTACAGGCGTATG | 267 |
| rs770921967 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56408490 | TCTTTCTCAATCTTG[C/T]TCTAGTCCTCCTCTC | 267 |
| rs770995709 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56415285 | GACCTTGATAAAAAC[A/G]GTACAGATGACTTGT | 267 |
| rs771033009 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413863 | GAAGAAAAACAGCTA[C/T]AAAAAACAATATTGG | 267 |
| rs771076863 | snp | A/C/G | 6.84619e-05 | 0.00585038 | synonymous-codon, missense | AMFR | GRCh38.p7 | 16:56363026 | GCTCTCTGAGGCCGC[A/C/G]TCATCTTCAGAACTT | 267 |
| rs771262909 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56401914 | AACACCACTTGATAG[A/C]CTGCGCCTGTATCAC | 267 |
| rs771284283 | snp | C/G | 5.18059e-05 | 0.00508923 | missense | AMFR | GRCh38.p7 | 16:56408087 | GACTCGACCGTGGCT[C/G]CTCATCGGCGTGGTG | 267 |
| rs771312642 | in-del | -/TT | 2.02821e-05 | 0.00318444 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362146 | GCTTGCTGCCTAACC[-/TT]ACTCCCCAGGTCCAG | 267 |
| rs771314193 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56401221 | ATCTGGAAGGATTAC[A/G]GAAGAGACTATTTGT | 267 |
| rs771371041 | in-del | -/ACAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56365592 | AACATGTAGGTACAT[-/ACAC]ACACACGCACACACA | 267 |
| rs771396268 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56388915 | CTGAGGCTGCTTTAC[A/G]GTAAATTTTTTTTGT | 267 |
| rs771401040 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391952 | CGAGTAGCCTAACTG[C/T]GAGGCACCCCCCAGT | 267 |
| rs771421788 | snp | C/T | 0.000159599 | 0.00893162 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362323 | CTTCATCACACCCTA[C/T]AGCCCTGGACTTTCC | 267 |
| rs771479216 | in-del | -/GA | | | intron-variant | AMFR | GRCh38.p7 | 16:56385407 | GATCACTAAGGCCAG[-/GA]GAGTTCGAGACCAGA | 267 |
| rs771490348 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56398672 | AACAAAACCACAACA[C/T]ATCCAAACTTATGAG | 267 |
| rs771491275 | in-del | -/TT | | | intron-variant | AMFR | GRCh38.p7 | 16:56370561 | GTTAAAAAGGGTAAA[-/TT]TTTACTCTATTTCAA | 267 |
| rs771493279 | in-del | -/AGAG | 0.000100184 | 0.00707685 | intron-variant | AMFR | GRCh38.p7 | 16:56403122 | GTTGCCAAATAACTT[-/AGAG]AGAAAGAGAATAAAA | 267 |
| rs771501323 | snp | C/T | 0.000116195 | 0.00762129 | missense | AMFR | GRCh38.p7 | 16:56408023 | CGGTGATGGAGCAGA[C/T]GGCCGCCAGTCCACA | 267 |
| rs771618340 | snp | A/G | 1.78525e-05 | 0.00298763 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362453 | ACATGCTTCCACAAC[A/G]ACGACAGCAGTTTGA | 267 |
| rs771627756 | in-del | -/CC | | | intron-variant | AMFR | GRCh38.p7 | 16:56384735 | CACACACACACACAC[-/CC]ACTCAATTTTTGGAG | 267 |
| rs771659353 | in-del | -/AA | | | intron-variant | AMFR | GRCh38.p7 | 16:56364899 | CCTAAGGATCTTTTG[-/AA]AAAAGACACAGGATG | 267 |
| rs771672088 | snp | C/G | 5.32212e-05 | 0.00515827 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362638 | CTTCCTCCTGATCGT[C/G]CCCCACCCCAAGCAG | 267 |
| rs771734866 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379856 | CCCCTGTGGCTGTGC[A/T]GGGTACAGCCTCCCT | 267 |
| rs771747469 | in-del | -/CAGTC | 0.000248319 | 0.0111399 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362651 | GTCCCCCACCCCAAG[-/CAGTC]CAGTCAACACCAGAA | 267 |
| rs771750137 | snp | A/G | 0.000118804 | 0.00770636 | missense | AMFR | GRCh38.p7 | 16:56362943 | TGAAGCCTCCGTTCC[A/G]CGGCGGCAGCCAGCA | 267 |
| rs771759884 | snp | C/T | 7.10152e-05 | 0.0059584 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362557 | GGTGCTCAGGACACC[C/T]GCATTTGTGGGACGT | 267 |
| rs771797238 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56395895 | CCAATAACAGACAAA[C/T]AGAGAGCCAAATCAT | 267 |
| rs771818944 | in-del | -/AGTA | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425973 | TTTCTGCTGTTTGCT[-/AGTA]AGTAGCCTCCAGCAG | 267 |
| rs771833136 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387741 | CTGCCGGGAGGCAGA[A/T]CATTTATATTTTATG | 267 |
| rs771838908 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56371160 | GTCCATAAAAACCTC[G/T]AAAATCAGATAAAAC | 267 |
| rs771891961 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370193 | TTAAAGCTCAAAATA[G/T]CTTGGGTATAAAAAT | 267 |
| rs771935701 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | AMFR | GRCh38.p7 | 16:56367484 | TGGTCACTGCTTGGC[C/T]TTTCCACAGGACTGT | 267 |
| rs771980439 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423156 | GGAAGGCTTTTGAGA[C/T]TGTCACTTCTACTCA | 267 |
| rs771983647 | snp | A/G | 1.65326e-05 | 0.00287507 | missense | AMFR | GRCh38.p7 | 16:56404932 | GAATATGGTGCATGA[A/G]GTCCAGGGACAGGAG | 267 |
| rs772102828 | in-del | -/ATAT | | | intron-variant | AMFR | GRCh38.p7 | 16:56397688 | ATAATAAATACATAC[-/ATAT]ATTTTATATATAATC | 267 |
| rs772111343 | snp | C/T | 1.65559e-05 | 0.00287709 | missense | AMFR | GRCh38.p7 | 16:56408014 | GGGTGTAGCCGGTGA[C/T]GGAGCAGACGGCCGC | 267 |
| rs772155176 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56365869 | TGTTATTCAAGGACT[C/T]TGTATTTCTTCACAA | 267 |
| rs772193298 | snp | A/G | 3.53213e-05 | 0.00420231 | intron-variant | AMFR | GRCh38.p7 | 16:56405257 | AGACTATAAAAAAGG[A/G]TATTTTCTTTTTAGT | 267 |
| rs772265820 | snp | A/G | 1.73366e-05 | 0.00294415 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362882 | GGGCACAGGGCGCAG[A/G]AGGCAGCTGAGGAAG | 267 |
| rs772267574 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372090 | ATTCATGGATTTTGG[C/T]ATCTGAAGGAGGGGG | 267 |
| rs772309307 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56415548 | CTTAAGGGCAGCCCT[C/G]ATTCATTACAAATGA | 267 |
| rs772415642 | snp | C/T | 1.7736e-05 | 0.00297787 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362318 | GGTGACTTCATCACA[C/T]CCTATAGCCCTGGAC | 267 |
| rs772480077 | in-del | -/AATAA | 1.68597e-05 | 0.00290337 | intron-variant | AMFR | GRCh38.p7 | 16:56403134 | CTTAGAGAGAAAGAG[-/AATAA]AACACACGGTAAAAG | 267 |
| rs772504579 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385852 | TCATATACCCGGCAC[A/T]CACGCTCTAGCTGTT | 267 |
| rs772556860 | snp | G/T | 1.65135e-05 | 0.00287341 | missense | AMFR | GRCh38.p7 | 16:56363978 | ATGCGCTGTCTCTCA[G/T]CAGCAGACTTGGAGA | 267 |
| rs772565599 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411484 | CCTGGGCTCAAGTGA[A/T]CCCACCTTGGTCTCC | 267 |
| rs772611146 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56373660 | GGGAATTTAAAACTA[G/T]GATTAATATGCAAAG | 267 |
| rs772660134 | snp | C/T | 1.77543e-05 | 0.0029794 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362559 | TGCTCAGGACACCTG[C/T]ATTTGTGGGACGTAC | 267 |
| rs772753394 | snp | C/T | 8.39074e-05 | 0.00647662 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364061 | CTCGCCGAAGTCCAG[C/T]GTCTCCTCCAGGCGA | 267 |
| rs772787732 | snp | A/G | 5.8148e-05 | 0.00539172 | intron-variant | AMFR | GRCh38.p7 | 16:56408128 | AAAGCTGAAATGCAC[A/G]CAGTAGGAAACTGCT | 267 |
| rs772843549 | snp | A/G | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56389266 | CCAAATTCTCATCCA[A/G]GTTCTCTCCTTGATG | 267 |
| rs772907883 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | AMFR | GRCh38.p7 | 16:56402985 | CTTGTGCTTCCTTAC[C/G]TGGCCTCCATGTTTC | 267 |
| rs772931294 | in-del | -/CTT | | | intron-variant | AMFR | GRCh38.p7 | 16:56367916 | GCTGCTGTTACCGTC[-/CTT]CTTCTAGCCAGTTTA | 267 |
| rs772964592 | in-del | -/CGACACCG | 1.74139e-05 | 0.0029507 | intron-variant | AMFR | GRCh38.p7 | 16:56405247 | CACAAGAAGAGACTA[-/CGACACCG]TAAAAAAGGATATTT | 267 |
| rs772985387 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56405625 | CTGCTATCCTAGACA[C/G]GAGGACCTGCTCTCT | 267 |
| rs772989699 | snp | C/T | 5.09074e-05 | 0.00504491 | intron-variant | AMFR | GRCh38.p7 | 16:56403141 | AGAAAGAGAATAAAA[C/T]ACACGGTAAAAGCGA | 267 |
| rs772990754 | snp | C/T | 1.65949e-05 | 0.00288048 | synonymous-codon | AMFR | GRCh38.p7 | 16:56409427 | CTAAAAACTCACATA[C/T]TCAAATCGATCCTTG | 267 |
| rs772998892 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389237 | AGGTCTCCCTTCGGC[C/T]GCTGCTACAGGAACC | 267 |
| rs773108149 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379683 | GTTCCAAATGGGAGA[A/G]ATTGGCCAAAACAAA | 267 |
| rs773117196 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | AMFR | GRCh38.p7 | 16:56367490 | CTGCTTGGCCTTTCC[A/G]CAGGACTGTTCAATG | 267 |
| rs773128761 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56417711 | GATGTATATGAAACA[C/G]AGGAATTTCATGTTT | 267 |
| rs773202299 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403650 | AACAACCAAATATAA[C/T]CTAAATAACCCATTG | 267 |
| rs773228441 | snp | C/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425985 | TGCTAGTAGCCTCCA[C/G]CAGAAACTAAAAAAT | 267 |
| rs773233341 | snp | C/G/T | 0.000208582 | 0.0102105 | intron-variant | AMFR | GRCh38.p7 | 16:56386045 | AAACAAGAATCCAGT[C/G/T]TAAGTTTCAGAGCCC | 267 |
| rs773271833 | snp | C/T | 0.000681663 | 0.018449 | missense, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425225 | CGGGCTGGCTGAGCG[C/T]GCGGTAGGCGCTGAT | 267 |
| rs773301574 | snp | C/T | 5.29638e-05 | 0.00514578 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362817 | CAATGCAGTCAAGCC[C/T]GCTTTTCCATGGAGC | 267 |
| rs773316722 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56372256 | ATTTCGCCTCGCCTC[A/G]CCCCAGCCCTCCTGC | 267 |
| rs773320652 | snp | A/G | 1.73117e-05 | 0.00294203 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362888 | AGGGCGCAGGAGGCA[A/G]CTGAGGAAGGCAAGG | 267 |
| rs773332021 | snp | C/G | 1.65507e-05 | 0.00287664 | missense | AMFR | GRCh38.p7 | 16:56408016 | GTGTAGCCGGTGATG[C/G]AGCAGACGGCCGCCA | 267 |
| rs773352248 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56414713 | TCATTTCCGACATTA[-/T]TTTTGACAGCCTTGA | 267 |
| rs773463953 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419021 | TCTGTATCCCTTAAC[-/T]TTTTTTTTTTTTTTT | 267 |
| rs773550929 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363149 | CATCTCCCCATGTCC[A/T]GGCACCTTCATGAAG | 267 |
| rs773628738 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56399207 | AGACCCCTCAGGTAT[C/T]GTTGGGGGAATATCA | 267 |
| rs773657871 | snp | A/G | 3.57603e-05 | 0.00422834 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362237 | AGCACCAGAGTTCAC[A/G]GAAATCAAGCCGGCT | 267 |
| rs773695075 | snp | A/G | 1.77454e-05 | 0.00297866 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362356 | TCCTCTGCTCCAGGT[A/G]TCGAACCAAGAGTTC | 267 |
| rs773701831 | snp | A/T | 1.77745e-05 | 0.00298109 | intron-variant | AMFR | GRCh38.p7 | 16:56405260 | CTATAAAAAAGGATA[A/T]TTTCTTTTTAGTAAA | 267 |
| rs773724208 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382630 | CCTGCAGGTTGGACA[A/G]GCTTGGTACAAAGTT | 267 |
| rs773751728 | snp | A/G | 1.65222e-05 | 0.00287417 | synonymous-codon | AMFR | GRCh38.p7 | 16:56363989 | CTCATCAGCAGACTT[A/G]GAGAAGCGGCTCCCA | 267 |
| rs773814282 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | AMFR | GRCh38.p7 | 16:56367472 | TCTCCCTCTTCCTGG[C/T]CACTGCTTGGCCTTT | 267 |
| rs773819308 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56420854 | CCAAGCAGCTAGGAC[C/T]ACAGCACAGGCCACT | 267 |
| rs773857891 | snp | C/T | 1.77357e-05 | 0.00297784 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362321 | GACTTCATCACACCC[C/T]ATAGCCCTGGACTTT | 267 |
| rs773904261 | snp | C/G | 1.65444e-05 | 0.00287609 | missense | AMFR | GRCh38.p7 | 16:56403102 | CTGGCCATGGATAAC[C/G]AGATGTTGCCAAATA | 267 |
| rs773948305 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56422865 | ATTGTGTTTGTTCAT[A/G]AAAAACCTCCTGTGA | 267 |
| rs773963727 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56404098 | AGAGTACAGTGGCGC[C/G]ATCTCAGCTCACTGC | 267 |
| rs773986657 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379770 | TCCAAAATGATCTCC[A/G]CTGAATCCATGTCTC | 267 |
| rs774023312 | snp | A/C/G | 3.31001e-05 | 0.00406807 | missense | AMFR | GRCh38.p7 | 16:56408028 | ATGGAGCAGACGGCC[A/C/G]CCAGTCCACAGCAGG | 267 |
| rs774043243 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379126 | GCTGATAAAGATATA[A/T]CCGAGACTGGCAATT | 267 |
| rs774044432 | snp | C/T | 1.65261e-05 | 0.0028745 | missense | AMFR | GRCh38.p7 | 16:56414266 | CCTGTCTCTCACTCA[C/T]TCGAAGAGGGCCAAA | 267 |
| rs774049418 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56405744 | TTTAATCCCAGCACT[C/T]TGGGAGACCGAGGCA | 267 |
| rs774068358 | snp | C/G | 1.78694e-05 | 0.00298905 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362472 | ACAGCAGTTTGATAA[C/G]AGATGTTACCCCACG | 267 |
| rs774115765 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387710 | AGTGTGGTTTTCATT[A/G]CAACTCCTTTTAACA | 267 |
| rs774135705 | snp | A/C | 1.71314e-05 | 0.00292667 | intron-variant | AMFR | GRCh38.p7 | 16:56414396 | CTGCTGAAAAATAAA[A/C]GCAGCTCTAAAAATC | 267 |
| rs774172277 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402513 | CTTGCACCTCCAGGC[A/G]TGGCTTAGCCCCAGC | 267 |
| rs774193091 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56392309 | AAAATCAGAGTGCCT[C/G]TCCTCCTCCAAAGGA | 267 |
| rs774236186 | snp | C/T | 1.74151e-05 | 0.0029508 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362877 | CAGTCGGGCACAGGG[C/T]GCAGGAGGCAGCTGA | 267 |
| rs774269890 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant | AMFR | GRCh38.p7 | 16:56402965 | GTAAACTTAGGCAAC[A/G]TCAACTTGTGCTTCC | 267 |
| rs774276090 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56408511 | TCCTCCTCTCTGAAA[C/T]TGGCATTCCTAGTCT | 267 |
| rs774330019 | snp | G/T | 1.76852e-05 | 0.0029736 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362801 | ATGCTTTATACAGCG[G/T]CAATGCAGTCAAGCC | 267 |
| rs774341020 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56376970 | AATAGACAATGTGAA[A/G]TTGTATAGATAATTA | 267 |
| rs774356174 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379848 | CAGCTCCACCCCTGT[A/G]GCTGTGCAGGGTACA | 267 |
| rs774358413 | snp | A/C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386869 | TTTGGGAGGCTAAGG[A/C/T]GGGCAGATCACAAGG | 267 |
| rs774427539 | snp | A/G | 1.65198e-05 | 0.00287395 | missense | AMFR | GRCh38.p7 | 16:56369324 | TCTCTTGAATCTGAT[A/G]AGCCTACAGGAATAC | 267 |
| rs774515029 | snp | A/G | 1.65477e-05 | 0.00287638 | intron-variant | AMFR | GRCh38.p7 | 16:56405081 | TAGTAATTTACTGTT[A/G]CTACTGAATTTGGTT | 267 |
| rs774552973 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56371998 | GTTATATACAAACAG[C/T]ATCCTTCCCCCATCT | 267 |
| rs774648036 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56415340 | AATTCAATGTAAAGC[C/T]GCTTCTGCCTCTGAT | 267 |
| rs774659322 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56365670 | GACCCTAGAGCAGGT[C/T]AGAAAAAATGGTGAG | 267 |
| rs774682028 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371616 | CACTCTCTGTTGGCA[A/G]TCCAGCTGAGGTTTA | 267 |
| rs774682390 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383594 | CAGTACGTGGTACCA[C/G]TGTCAACTCAGCTGC | 267 |
| rs774732352 | snp | A/G | 2.14337e-05 | 0.00327359 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362131 | AAAACCATAAACCAA[A/G]GCTTGCTGCCTAACC | 267 |
| rs774737447 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56382899 | ACCCAGGCTGTTAAG[A/G]GGGCGTGGGAGCTGG | 267 |
| rs774757134 | in-del | -/GAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56412553 | TTTGAAGAGAAACTT[-/GAA]GAAGTATCAAAAGAA | 267 |
| rs774770138 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56372462 | ATCCATCCATCTCCA[A/G]TAGACATTTCAGTTG | 267 |
| rs774830072 | in-del | -/GA | 3.70199e-05 | 0.00430216 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362180 | GGACAAGGAAATGCT[-/GA]GAGGGGAGGGGACCC | 267 |
| rs774851278 | in-del | -/TAGA | | | intron-variant | AMFR | GRCh38.p7 | 16:56390876 | GTGAGTACAACTAGT[-/TAGA]TAGATATAGTTTTCT | 267 |
| rs774858942 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402319 | CCAGCCTGGGTGAGT[A/G]AGACTCCATCTCCAA | 267 |
| rs774895041 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56423374 | TGCCAGAGGTAAGAC[C/G]TCTACTGAAAATGCT | 267 |
| rs774902188 | snp | G/T | 1.78258e-05 | 0.00298539 | intron-variant | AMFR | GRCh38.p7 | 16:56389413 | ATACGTCAGCATCCT[G/T]GATTGTTCCTTAGCA | 267 |
| rs774911930 | snp | A/C/T | 4.95727e-05 | 0.00497838 | missense | AMFR | GRCh38.p7 | 16:56401805 | ATGGCACAGTCGTCA[A/C/T]TGTTGACAGCCAGCT | 267 |
| rs774970088 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56410396 | AAATGCTGCCTTAAC[A/G]TTTTTATGAATTTTC | 267 |
| rs774999426 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | AMFR | GRCh38.p7 | 16:56402938 | TCTGCTGTTATTAAA[A/G]AACTAAAATGAGTAA | 267 |
| rs775062351 | in-del | -/CAG | 1.77413e-05 | 0.00297831 | utr-variant-3-prime, cds-indel | AMFR | GRCh38.p7 | 16:56362666 | CAGTCCAGTCAACAC[-/CAG]AAGAGATCATACCTA | 267 |
| rs775118308 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380734 | TTTGCTAAAACATGA[C/T]AAGAGTCACCCTTGC | 267 |
| rs775195940 | snp | C/T | 1.71284e-05 | 0.00292642 | missense | AMFR | GRCh38.p7 | 16:56364086 | AGGCGAGGACTGAGG[C/T]CCAGTGGCACACGCT | 267 |
| rs775201893 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56370848 | TCTAATAACTATAAC[-/A]AAAAAAGGAAGAAAA | 267 |
| rs775303143 | snp | C/G | 1.77052e-05 | 0.00297528 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362789 | CTATAAGACCACATG[C/G]TTTATACAGCGGCAA | 267 |
| rs775306108 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56387898 | TGAGCTAATTAAGTG[A/T]GCTCCTTGAAGGCAT | 267 |
| rs775343224 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377027 | GCCCACATGAGTTCG[C/T]TAGTGAATTCTGCCA | 267 |
| rs775402199 | snp | G/T | 1.65784e-05 | 0.00287905 | intron-variant | AMFR | GRCh38.p7 | 16:56414242 | ATCCATCCTTTCAGT[G/T]TAGACTTACCTGTCT | 267 |
| rs775420765 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56375981 | GAGAATCGCTTGAAC[A/C]CAGGAGGTGGAGGTT | 267 |
| rs775435309 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56364555 | AATTGACTCTGAAAA[C/T]AGAGGTAAAAAGGAA | 267 |
| rs775459215 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56368746 | GAAGGCCAAGTTCAC[C/T]ACTCTATTTATTTTT | 267 |
| rs775475238 | snp | C/T | 1.64914e-05 | 0.00287149 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369310 | AACCTGGGGAAACAT[C/T]TCTTGAATCTGATGA | 267 |
| rs775499421 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56401336 | TTAAGGCTTCTTTTG[C/G]GCATGTACAAAATGC | 267 |
| rs775500202 | snp | A/G | 1.74708e-05 | 0.00295552 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362109 | TAATTTACTTCACCA[A/G]TGAATGAAAACCATA | 267 |
| rs775512874 | snp | C/T | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56404909 | TCTGAGGAAACTTAC[C/T]AACATGTGAATATGG | 267 |
| rs775589387 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56383048 | TACACCCTATCAAGC[C/T]ACCACCTCTACTGCT | 267 |
| rs775652347 | snp | A/G/T | 6.59767e-05 | 0.00574324 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389234 | GCGAGGTCTCCCTTC[A/G/T]GCTGCTGCTACAGGA | 267 |
| rs775653247 | snp | C/T | 4.9516e-05 | 0.00497549 | synonymous-codon | AMFR | GRCh38.p7 | 16:56404984 | TGTGTAATAGACATA[C/T]GTCCCCTTTCCTTCC | 267 |
| rs775682761 | snp | A/T | 1.82427e-05 | 0.0030201 | missense | AMFR | GRCh38.p7 | 16:56363046 | CTTCAGAACTTTTGT[A/T]CAAGAAACGTCTAGA | 267 |
| rs775766832 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56409137 | TATTGTTTATGTATC[A/C]AGGTTTCCTTGCACT | 267 |
| rs775767188 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56385414 | TAAGGCCAGGAGTTC[A/G]AGACCAGACTGGCCA | 267 |
| rs775787360 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56423454 | ACAGCTTTTATGTAA[C/T]GTTTTCTGAAGAGAT | 267 |
| rs775823332 | in-del | -/AAT | | | intron-variant | AMFR | GRCh38.p7 | 16:56403134 | CTTAGAGAGAAAGAG[-/AAT]AAAACACACGGTAAA | 267 |
| rs775848543 | snp | A/G | 6.705e-05 | 0.00578969 | missense | AMFR | GRCh38.p7 | 16:56362985 | AGGGTCACGGGGTCA[A/G]AGGACGCACCTTCCG | 267 |
| rs775851488 | snp | A/G | 1.65433e-05 | 0.002876 | intron-variant | AMFR | GRCh38.p7 | 16:56405068 | AGAGAAAACACCTTA[A/G]TAATTTACTGTTACT | 267 |
| rs775875230 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56411666 | TTTTGTAGAGAACAA[A/C]ATAAAGTGGAAAAAA | 267 |
| rs775875920 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56389814 | CCACCAGCACAGTCA[C/T]CACCTTGGCTTGTCT | 267 |
| rs775902676 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56420312 | AGCACCACTCCCCTG[A/C]GCCCCCTACCATTTG | 267 |
| rs775934391 | snp | C/G/T | 3.3177e-05 | 0.00407279 | intron-variant | AMFR | GRCh38.p7 | 16:56401684 | CACAAAGCACACACA[C/G/T]GCCCTGGACAGAACA | 267 |
| rs776069517 | snp | A/C | 1.77432e-05 | 0.00297847 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362655 | CCCACCCCAAGCAGT[A/C]CAGTCAACACCAGAA | 267 |
| rs776226257 | in-del | -/GGGCCAACCAAT | 1.70525e-05 | 0.00291992 | cds-indel | AMFR | GRCh38.p7 | 16:56405237 | TCCTCACTGTCACAA[-/GGGCCAACCAAT]GAAGAGACTATAAAA | 267 |
| rs776362709 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388057 | CACTTTCAATTAAAA[C/T]TGAAATACAGTCAAT | 267 |
| rs776404932 | snp | C/G | 1.6552e-05 | 0.00287676 | intron-variant | AMFR | GRCh38.p7 | 16:56363100 | TCATAGGAGAGATGG[C/G]GAGCTGTGGAACACA | 267 |
| rs776407814 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56366901 | GGCACCCAAAGTGGG[C/T]CAACAAACAGATCTG | 267 |
| rs776445103 | snp | G/T | 1.64749e-05 | 0.00287005 | synonymous-codon | AMFR | GRCh38.p7 | 16:56369268 | TGAGCGTGTCAGCTG[G/T]AGGTCCTGCAGTACC | 267 |
| rs776461190 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56378048 | AGATTCAATGCAATC[C/T]CAATTAATATCCCAG | 267 |
| rs776570670 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56399659 | AGGAAGGAATGGAGA[A/G]CACTTACTTAGTGAC | 267 |
| rs776615377 | snp | A/C/G | 3.30018e-05 | 0.00406202 | missense | AMFR | GRCh38.p7 | 16:56404974 | TGACAAAGTCTGTGT[A/C/G]ATAGACATACGTCCC | 267 |
| rs776641323 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416531 | GCTCACTGCAACCTC[A/G]GCCTTCCAGGTTCAA | 267 |
| rs776641329 | snp | C/T | 3.55063e-05 | 0.0042133 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362570 | CCTGCATTTGTGGGA[C/T]GTACGCATGAGGCAG | 267 |
| rs776654452 | snp | A/G | 1.68202e-05 | 0.00289996 | stop-gained | AMFR | GRCh38.p7 | 16:56362965 | CAGCCAGCATCCTTC[A/G]ACGCAGGGTCACGGG | 267 |
| rs776730284 | snp | G/T | 1.72782e-05 | 0.00293918 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362891 | GCGCAGGAGGCAGCT[G/T]AGGAAGGCAAGGGAG | 267 |
| rs776742401 | snp | C/T | 0.000116781 | 0.00764046 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389210 | GAAGAAGTGATTGTG[C/T]TGGTTTAAGCGAGGT | 267 |
| rs776801722 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56411849 | GGTGCAGGGAAAGTA[C/T]AAGGTGAACTTAGGA | 267 |
| rs776853946 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363214 | CAGCCCCCAACAGAT[A/G]GGCGCAAATTCTCTC | 267 |
| rs776895139 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56403386 | CCATGCAATTATAAA[A/G]CAGAAAATATGAAAA | 267 |
| rs776968147 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379831 | GTTTCCGTGGTCTTG[A/G]GCAGCTCCACCCCTG | 267 |
| rs777037216 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56412670 | TTTGAGACCAACCTG[A/G]GCAGCATGGTGAAAT | 267 |
| rs777065135 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56405942 | GCAGTAAGCAGAGAT[C/T]GCACCACAGCACTCC | 267 |
| rs777077526 | snp | C/T | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361888 | GATTTGGGACCTGGG[C/T]CCTCTCCAAGGCAGG | 267 |
| rs777108965 | snp | A/G | 5.27677e-05 | 0.00513625 | intron-variant | AMFR | GRCh38.p7 | 16:56386057 | AGTGTAAGTTTCAGA[A/G]CCCTGACTCTTTCCC | 267 |
| rs777179216 | snp | G/T | 3.54704e-05 | 0.00421117 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362336 | TATAGCCCTGGACTT[G/T]CCCCTCCTCTGCTCC | 267 |
| rs777186880 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56411083 | TTACACAGAGGGCTT[-/C]CCAGTTTTAACAATC | 267 |
| rs777235519 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56374993 | TTGTTTTGTTATCAA[A/G]AGGTACTCACACTTC | 267 |
| rs777286921 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386314 | CCAAGATCACACAGT[G/T]TAACTATGATGGCCA | 267 |
| rs777288075 | snp | C/T | 4.94214e-05 | 0.00497074 | missense | AMFR | GRCh38.p7 | 16:56369257 | GTTATTTCAACTGAG[C/T]GTGTCAGCTGGAGGT | 267 |
| rs777323090 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56412919 | CCTCTAGAGTCGATA[A/C]TGGAGAAAGTGCTGA | 267 |
| rs777381552 | snp | C/G | 1.65127e-05 | 0.00287334 | missense | AMFR | GRCh38.p7 | 16:56405028 | GGTTGAGGTCCCAGA[C/G]GTGAATTACGTATCT | 267 |
| rs777403160 | snp | A/G | 1.85834e-05 | 0.00304817 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362177 | ACGGGACAAGGAAAT[A/G]CTGAGAGGGGAGGGG | 267 |
| rs777403660 | snp | A/C | 1.77407e-05 | 0.00297826 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362642 | CTCCTGATCGTCCCC[A/C]ACCCCAAGCAGTCCA | 267 |
| rs777406344 | snp | C/T | 8.51158e-05 | 0.00652309 | missense | AMFR | GRCh38.p7 | 16:56363022 | GGAAGCTCTCTGAGG[C/T]CGCATCATCTTCAGA | 267 |
| rs777424747 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380375 | GCCTCTGGGCCTGTG[A/T]TGAGAGGGGGCTGCT | 267 |
| rs777487630 | snp | A/G | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56426987 | CTCAGCCCAGAGTAG[A/G]TGCTCTGTAAATATT | 267 |
| rs777648221 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56419902 | CCAAATGCCTTTTTT[G/T]TCCAGTCTACACAAA | 267 |
| rs777689853 | snp | A/G | 1.69591e-05 | 0.00291191 | synonymous-codon | AMFR | GRCh38.p7 | 16:56362945 | AAGCCTCCGTTCCGC[A/G]GCGGCAGCCAGCATC | 267 |
| rs777705255 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56418386 | GTGCTCTCCTGTAAT[C/T]CCAGCTAGTCAGGAG | 267 |
| rs777711748 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56409358 | GCTGTGGCTCATTCA[C/T]ATTACACAATTCAAA | 267 |
| rs777791437 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388473 | CAGACTTTATAAACA[C/T]TGTACACTTAGGCTA | 267 |
| rs777802901 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56387148 | AAGGTCTTGAGATGG[A/G]TACAAACAAAACGTA | 267 |
| rs777855851 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385019 | ATGGGCCAGGCTGGT[C/T]TCGAACTCTTGACCT | 267 |
| rs777942592 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56370921 | TAGCTCCTAGGGACA[C/T]GTTGTTCTGACTATA | 267 |
| rs777980740 | snp | A/G | 7.11491e-05 | 0.00596401 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362513 | GGGCTCACACTGTGC[A/G]CCTCCCCCACACTCT | 267 |
| rs777983546 | snp | C/T | 1.73628e-05 | 0.00294637 | intron-variant | AMFR | GRCh38.p7 | 16:56389170 | GTATAGTTTCAGAGG[C/T]TGAAACCAACTAACC | 267 |
| rs778038146 | snp | C/T | 1.67024e-05 | 0.0028898 | intron-variant | AMFR | GRCh38.p7 | 16:56401876 | GCCCAGCAGGAACCT[C/T]AGTCAGTTCCACACG | 267 |
| rs778069364 | snp | G/T | 1.78484e-05 | 0.00298728 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362444 | GCACAGTCTACATGC[G/T]TCCACAACAACGACA | 267 |
| rs778073862 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56376758 | TGAGAGCAGACATCA[A/G]TGAAACTGAAAATAA | 267 |
| rs778150651 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | AMFR | GRCh38.p7 | 16:56403040 | GCCGACGAATTCGAC[A/G]TTGCACCTCATGAAA | 267 |
| rs778240879 | snp | C/G | 9.3769e-05 | 0.00684659 | utr-variant-5-prime, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56425337 | CGGCATGGCGGCAGC[C/G]GCGACCTCTGGCCCC | 267 |
| rs778334199 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413471 | AGTGAGCTGAGATTG[C/T]GCCACTGCACTGCAG | 267 |
| rs778351187 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416091 | ATGCCCCAGCTTTAT[A/T]ACGACGCAATTTCTT | 267 |
| rs778358370 | snp | A/T | 4.97385e-05 | 0.00498666 | missense | AMFR | GRCh38.p7 | 16:56404919 | CTTACCAACATGTGA[A/T]TATGGTGCATGAGGT | 267 |
| rs778374603 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56363746 | GACCAGTGGGGCCCA[A/G]TGTTACCAGATGCTC | 267 |
| rs778425901 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363067 | AACGTCTAGAAAAAA[C/T]AGAAGACTTTTTCTC | 267 |
| rs778439563 | snp | C/G | 2.08184e-05 | 0.00322626 | intron-variant | AMFR | GRCh38.p7 | 16:56364150 | GCTGTGAGCACAGGC[C/G]TCCCTCCTAAGCAGG | 267 |
| rs778479945 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56414736 | AGCCTTGAAGAAAAC[C/T]GTTCTAGAAATTGAA | 267 |
| rs778484637 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56367320 | TTGGGATGGATACAG[C/G]ACAGTTTCTTTTGTA | 267 |
| rs778522099 | snp | C/G | 1.74561e-05 | 0.00295428 | intron-variant | AMFR | GRCh38.p7 | 16:56389160 | CACCCCTTAGGTATA[C/G]TTTCAGAGGTTGAAA | 267 |
| rs778524108 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56385620 | CTCCAGAAAAAAAAA[-/T]TTTTTTTTTTTTTGG | 267 |
| rs778540995 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371047 | CATAAGCAGTGCCCA[A/G]GGCCCCCAGGGCCTC | 267 |
| rs778552647 | snp | A/C | 1.65168e-05 | 0.00287369 | intron-variant | AMFR | GRCh38.p7 | 16:56367574 | GAGTCACACAGAAAT[A/C]AAATCACAGACTCAG | 267 |
| rs778554215 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56398552 | TCTTTGATAATTTAA[C/G]TGAAATTTGCTCTTA | 267 |
| rs778557906 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56408251 | CATCCCATTACTATA[C/T]GGTCCTATTCTCCAA | 267 |
| rs778558679 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56403538 | AGTTCTGAAGGTCAA[-/T]TATGGGAAGATAGTA | 267 |
| rs778595777 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56393801 | TTAGACAGATCAACG[-/A]AGACAGAAAGTTAAC | 267 |
| rs778616404 | snp | C/T | 1.68301e-05 | 0.00290082 | synonymous-codon | AMFR | GRCh38.p7 | 16:56408069 | GGCAACCAACAGGGA[C/T]AGGACTCGACCGTGG | 267 |
| rs778619540 | snp | C/T | 5.07164e-05 | 0.00503544 | synonymous-codon | AMFR | GRCh38.p7 | 16:56363014 | CGAGGGGAGGAAGCT[C/T]TCTGAGGCCGCATCA | 267 |
| rs778643913 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400188 | TTGCCCAGGCTGGAG[A/T]ACAATGGCACGATCT | 267 |
| rs778659834 | in-del | -/AC | | | intron-variant | AMFR | GRCh38.p7 | 16:56384706 | CACATGCATACATAC[-/AC]ACACACACACACACA | 267 |
| rs778740312 | snp | C/T | | | | | GRCh38.p7 | 16:56420143 | AGGAAGGTGCATTTA[C/T]CACCATGTAACCCTA | 267 |
| rs778804937 | snp | A/C | 4.40917e-05 | 0.00469509 | intron-variant | AMFR | GRCh38.p7 | 16:56386040 | GAAACAAACAAGAAT[A/C]CAGTGTAAGTTTCAG | 267 |
| rs778835219 | snp | A/G | 1.77527e-05 | 0.00297927 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362286 | AAGTCAGTCCCAGAT[A/G]TAGTGGGACAGAAAG | 267 |
| rs778841402 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56400788 | CTTTAAAGCACTTAT[C/G]TCATTGATACTTTAA | 267 |
| rs778851293 | in-del | -/C | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362278 | GCTCGGAAAGTCAGT[-/C]CCCAGATGTAGTGGG | 267 |
| rs778855765 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56389859 | TCAAAATTCTCACTC[A/G]TTCACTCAAGCTCCT | 267 |
| rs778922910 | snp | A/G | 1.67175e-05 | 0.0028911 | synonymous-codon | AMFR | GRCh38.p7 | 16:56364052 | CACTTCCACCTCGCC[A/G]AAGTCCAGCGTCTCC | 267 |
| rs778963655 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56416122 | AAAATAATTCTTCCC[A/G]TTTTTACATGTAGTC | 267 |
| rs779003839 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56410613 | AGGGCCGGGCGTGGT[A/G]GCTCATGCACGAAAT | 267 |
| rs779027624 | snp | A/G | 1.82075e-05 | 0.00301719 | intron-variant | AMFR | GRCh38.p7 | 16:56364116 | TCGGTCTGGACACGG[A/G]GCAGGAAGCAAGGAG | 267 |
| rs779052758 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372178 | ACAGGCACATGGCTG[C/T]GCAACAGATCTGAAC | 267 |
| rs779099143 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388678 | TAAGAGTTTTTCTAT[G/T]TCTAAAAGTTTTAAT | 267 |
| rs779185046 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56401953 | TACAGAGAAAGCATG[C/T]TCAGCAAAACATTCT | 267 |
| rs779239673 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56416829 | CTCTTATAATCCCAT[C/T]ACCCATAGAACAACC | 267 |
| rs779252593 | in-del | -/C | 1.67349e-05 | 0.0028926 | intron-variant | AMFR | GRCh38.p7 | 16:56403122 | TTGCCAAATAACTTA[-/C]GAGAGAAAGAGAATA | 267 |
| rs779305070 | snp | A/G | 3.5517e-05 | 0.00421394 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362753 | TACAAAGAAGGATTA[A/G]ATTTATCAGCTGTCC | 267 |
| rs779323072 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56402871 | TCCAGAGCCTTTCCT[C/T]TCCACCACTCTATTA | 267 |
| rs779383697 | snp | A/G | 1.65211e-05 | 0.00287407 | synonymous-codon, utr-variant-5-prime | AMFR | GRCh38.p7 | 16:56414330 | CAAAACACAGCAAGC[A/G]GTATTTACTAGAACC | 267 |
| rs779400079 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56368144 | TGCGAGGGATATGTT[C/T]TGCACTGGATCCCAG | 267 |
| rs779454599 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56367384 | AGGAAGACCACTGTC[A/G]GGACCACATTCCCCC | 267 |
| rs779472861 | snp | C/T | 2.06639e-05 | 0.00321427 | intron-variant | AMFR | GRCh38.p7 | 16:56409629 | GTGAGTACCATCACA[C/T]CTACCCCATTTGAGG | 267 |
| rs779482214 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400586 | TTTACTCTCTGGGAT[C/T]GGCCACACAGCTTCT | 267 |
| rs779491672 | in-del | -/A | 0.001514 | 0.027472 | intron-variant | AMFR | GRCh38.p7 | 16:56414202 | CATAATACAAAGTTT[-/A]AAAAAAAAAAATCTA | 267 |
| rs779561530 | snp | A/G | 1.64779e-05 | 0.00287031 | missense | AMFR | GRCh38.p7 | 16:56403057 | TGCACCTCATGAAAC[A/G]GGTAACGCAGCTGCA | 267 |
| rs779573010 | snp | A/C | 1.66538e-05 | 0.00288559 | intron-variant | AMFR | GRCh38.p7 | 16:56401863 | GGAAACAAAACAAGC[A/C]CAGCAGGAACCTCAG | 267 |
| rs779587661 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56364193 | AGGGCACCCCAGACA[C/T]GGCTGTTCTGGACGC | 267 |
| rs779592691 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56415880 | ACAGCAAAACCTTGC[A/C]CCTACTGAAAAATAT | 267 |
| rs779635991 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390915 | AAAAAAAAAAATGCT[A/G]GAGTTCCTTAACTGA | 267 |
| rs779687659 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56388141 | ATTGTTGTGCGAACA[C/T]CATAGAGTATATTTA | 267 |
| rs779713102 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56421916 | GTAAAAACCCTGAAG[C/T]CTCCTCCCAAATCCT | 267 |
| rs779758485 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56422963 | AATATCTAGCAGGAC[C/T]TGCACTGGCAGAAGG | 267 |
| rs779780138 | snp | A/G | 1.7494e-05 | 0.00295748 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362869 | CCTCCAGTCAGTCGG[A/G]CACAGGGCGCAGGAG | 267 |
| rs779796513 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56371168 | AAACCTCTAAAATCA[C/G]ATAAAACTTCTCTTT | 267 |
| rs779881432 | snp | C/T | 1.77637e-05 | 0.00298019 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362278 | GGCTCGGAAAGTCAG[C/T]CCCAGATGTAGTGGG | 267 |
| rs779902209 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56390025 | CCTCAATGTCCTCCA[C/T]CCTCTTCTCTTTGCA | 267 |
| rs779945929 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56410036 | AAAATTAGCTGGGAA[C/T]GGTGGTGCACACCTG | 267 |
| rs779950173 | snp | A/G | 1.68007e-05 | 0.00289828 | missense | AMFR | GRCh38.p7 | 16:56405228 | ACATGAGCAGTCCTC[A/G]CTGTCACAAGAAGAG | 267 |
| rs779952471 | snp | A/C/T | 8.27033e-05 | 0.00643006 | missense, stop-gained | AMFR | GRCh38.p7 | 16:56363943 | CTTGCTGGAGGAGTT[A/C/T]GTCCTTACGCTGCAC | 267 |
| rs779957946 | snp | A/G | 2.0933e-05 | 0.00323513 | intron-variant | AMFR | GRCh38.p7 | 16:56385886 | TCCCTCCTAATTCCC[A/G]GTGATCTTCTTAAAG | 267 |
| rs780004281 | snp | A/G | | | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56361756 | GCTTTCAAAGAGTAA[A/G]AAAAAAAAAAAAAAA | 267 |
| rs780015147 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372274 | CCAGCCCTCCTGCAG[C/T]CATCATTCTGCTGTC | 267 |
| rs780042504 | snp | A/G | 1.64969e-05 | 0.00287196 | missense | AMFR | GRCh38.p7 | 16:56401764 | CACAGGGCAGTTTCC[A/G]CGCAGCCTGCATGGA | 267 |
| rs780079373 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379418 | TCAAGATGAGATTGG[A/G]GTGGGGACACAGTCA | 267 |
| rs780134330 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56391469 | AAAGCTGTGACAGAC[A/T]GCACCTGGAAAATCA | 267 |
| rs780153320 | snp | A/G | | | synonymous-codon | AMFR | GRCh38.p7 | 16:56367503 | CCACAGGACTGTTCA[A/G]TGCAGGTCTGATGCT | 267 |
| rs780200061 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56368327 | CCTTGTCCCAGGGTC[C/T]GCTTCTGGGGAAATC | 267 |
| rs780262112 | snp | C/G | 1.80879e-05 | 0.00300726 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362207 | GACCCATGGGGCACA[C/G]TCATGAGATGCAGGA | 267 |
| rs780371067 | snp | A/G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56418309 | AGGAGTTCAAGACCA[A/G/T]CCTGACCAACATGGT | 267 |
| rs780383915 | snp | C/T | | | upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56427244 | CAAGGTCTATATGAA[C/T]ACTAGACTTGAATTC | 267 |
| rs780426381 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56417359 | AGGCTGCAGGGAACC[A/G]TGATTGCACCACTGT | 267 |
| rs780442310 | in-del | -/T | 1.69143e-05 | 0.00290807 | intron-variant | AMFR | GRCh38.p7 | 16:56414392 | CTTCCTGCTGAAAAA[-/T]AAAAGCAGCTCTAAA | 267 |
| rs780460697 | snp | A/T | 1.6477e-05 | 0.00287024 | missense | AMFR | GRCh38.p7 | 16:56369228 | GAATCCGTCCTTCTA[A/T]AATATTGTCTGTTGT | 267 |
| rs780556191 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56375128 | ACACAGCTTTCAATG[A/C]AGCCCAATACAAATT | 267 |
| rs780612853 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56383523 | GCAACCCAGACTTAC[C/G]CAAATAGAACACCGC | 267 |
| rs780675300 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56385022 | GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCAG | 267 |
| rs780696416 | snp | A/C | 1.65433e-05 | 0.002876 | intron-variant | AMFR | GRCh38.p7 | 16:56414349 | TTTACTAGAACCTGT[A/C]AACAAATCAGAGAAA | 267 |
| rs780707336 | snp | C/T | 1.7736e-05 | 0.00297787 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362772 | TATCAGCTGTCCAAA[C/T]ACTATAAGACCACAT | 267 |
| rs780712483 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56398467 | GGATATAGATATATA[C/T]ATCCCTTGAAATGTA | 267 |
| rs780716975 | snp | A/G | 0.000105271 | 0.00725425 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362850 | GCAGAATTGGGACAG[A/G]CCTCCTCCAGTCAGT | 267 |
| rs780728279 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56402687 | GACAAATAAGAGCCT[A/G]ATACTGAGCACTATC | 267 |
| rs780797126 | snp | C/T | 2.1314e-05 | 0.00326444 | intron-variant | AMFR | GRCh38.p7 | 16:56385869 | ACGCTCTAGCTGTTC[C/T]TTCCCTCCTAATTCC | 267 |
| rs780831500 | snp | A/G | 1.82968e-05 | 0.00302457 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362190 | ATGCTGAGAGGGGAG[A/G]GGACCCATGGGGCAC | 267 |
| rs780953054 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56404537 | AAATCTGTGAAGTAG[C/T]TAACACTGCAGGAAT | 267 |
| rs781032837 | snp | C/T | 1.66443e-05 | 0.00288477 | missense | AMFR | GRCh38.p7 | 16:56363924 | GAAGCGACTCACTTG[C/T]GAGCTTGCTGGAGGA | 267 |
| rs781037190 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56379477 | CAAATCTCATGTCCT[C/T]ATGTTTCAGAACCAA | 267 |
| rs781077165 | snp | C/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56390156 | TAAAGAAAGGAAAGG[C/G]TACTAGAGTAAGAAG | 267 |
| rs781112290 | snp | C/T | 4.51091e-05 | 0.00474895 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362093 | AGGCTTTAGCACTGC[C/T]TAATTTACTTCACCA | 267 |
| rs781177548 | snp | A/G | 0.000118838 | 0.00770747 | intron-variant | AMFR | GRCh38.p7 | 16:56409387 | AAGTTGGCAAACGTG[A/G]TGACTAAGCAAGCAA | 267 |
| rs781209195 | snp | A/G | 1.65195e-05 | 0.00287393 | synonymous-codon | AMFR | GRCh38.p7 | 16:56389342 | GCATGTTGGACAGGA[A/G]GTGTCTTGTTCTAGC | 267 |
| rs781213397 | snp | G/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56369750 | ACAGTAGCAAAAATA[G/T]GGAATCAACCTAAGC | 267 |
| rs781218003 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56363781 | TTTTTCAAGAGAGGC[C/T]TGAAATCTGAGTTTT | 267 |
| rs781243460 | in-del | -/GCA | | | intron-variant, upstream-variant-2KB | AMFR | GRCh38.p7 | 16:56424354 | GAACATCAGGTAAAG[-/GCA]GCAGCAGAAAAGGAA | 267 |
| rs781262777 | snp | A/C | 1.65949e-05 | 0.00288048 | intron-variant | AMFR | GRCh38.p7 | 16:56405191 | CATCACCTCCCTCCC[A/C]AATTTCACTCACCGT | 267 |
| rs781266936 | in-del | -/AAA | | | intron-variant | AMFR | GRCh38.p7 | 16:56409725 | TCCTCAAGAAAACAG[-/AAA]AAAAAAAAAAAAAAA | 267 |
| rs781272447 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368587 | TTCTTATGCTCATCA[A/G]AGTAGAGATCTGAGC | 267 |
| rs781398150 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56407539 | GACGTGCGCCACCAC[A/G]CCCAACTAATTTTTT | 267 |
| rs781490599 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56377795 | ACATACTACAGTCAA[C/T]TGCTTTCCTATATAC | 267 |
| rs781521734 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56386508 | TCCTCTTTCACAAGC[C/T]ACACAAATGACTACT | 267 |
| rs781575370 | snp | C/G | 1.65127e-05 | 0.00287334 | intron-variant | AMFR | GRCh38.p7 | 16:56367567 | CAGTCCAGAGTCACA[C/G]AGAAATCAAATCACA | 267 |
| rs781579170 | in-del | -/C | 1.65975e-05 | 0.00288071 | intron-variant | AMFR | GRCh38.p7 | 16:56369182 | ATCATGCTTTAAAAG[-/C]CCAGTTTTACCTGTG | 267 |
| rs781596171 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56368042 | GGACTTTCTCTGGCT[A/G]CATGAGGTAGTTCAG | 267 |
| rs781612575 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56376236 | GCAGAAAATCAGTTA[A/T]GAACATAGCTGAACT | 267 |
| rs781624993 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56414878 | TAATATAAATATATA[C/T]ATACAGAGAGAATAT | 267 |
| rs781665563 | snp | A/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56413651 | ACTTTCCAATGTCAG[A/T]CAATCTCACCCAAAA | 267 |
| rs781681098 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56363872 | CAACGGCCTTCAGCC[A/C]CTAGTTTTTGATCTG | 267 |
| rs781720477 | snp | A/G | 0.000123967 | 0.00787199 | missense | AMFR | GRCh38.p7 | 16:56408094 | CCGTGGCTGCTCATC[A/G]GCGTGGTGGGCGAGA | 267 |
| rs781738792 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56380650 | TTCTACCAGATACTC[-/T]TAAATCATATGTCTC | 267 |
| rs781765810 | snp | A/C | 1.77637e-05 | 0.00298019 | utr-variant-3-prime | AMFR | GRCh38.p7 | 16:56362533 | CCCCACACTCTTCCC[A/C]CTGGGTGTGGTGCTC | 267 |
| rs796093331 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56372346 | TATTTCATGTAGCAT[-/T]AATGTCCTCCAGGTT | 267 |
| rs796128905 | in-del | -/AAT | | | intron-variant | AMFR | GRCh38.p7 | 16:56402356 | AATAATAATAATAAT[-/AAT]GGCTGCTGTTAGTGA | 267 |
| rs796172501 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56399093 | TTACTAAAAAAAAAA[-/A]CAAAATTCACCATAA | 267 |
| rs796344656 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374405 | GACAAAGGTAAAAAA[-/C]AAAAAAAAAAAAAAA | 267 |
| rs796408945 | multinucleotide-polymorphism | AA/TC | | | intron-variant | AMFR | GRCh38.p7 | 16:56392813 | TATCCAGAAGGACTT[AA/TC]CCAACCTAGGAAGGC | 267 |
| rs796415770 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56409748 | AAAAAAAAAAAAAAA[A/G]GCAGCCATCTGAAGA | 267 |
| rs796420508 | in-del | -/AAC | | | intron-variant | AMFR | GRCh38.p7 | 16:56374410 | AGGTAAAAAAAAAAA[-/AAC]AAAAAAAAAAAAACA | 267 |
| rs796452363 | in-del | -/GGAGAGAGGAGAGGAGAGAGGAGA | | | intron-variant | AMFR | GRCh38.p7 | 16:56406127 | GGGAGGGGGGAGAGG[-/GGAGAGAGGAGAGGAGAGAGGAGA]GGAGAGAGGAGAGGA | 267 |
| rs796585663 | snp | A/G | | | intron-variant | AMFR | GRCh38.p7 | 16:56379668 | TGGGTAAATACAGCT[A/G]TTCCAAATGGGAGAA | 267 |
| rs796627147 | in-del | -/TCTG | | | intron-variant | AMFR | GRCh38.p7 | 16:56390568 | TCCAAAATAATGTCA[-/TCTG]TCTGTATGTGTATAC | 267 |
| rs796685604 | in-del | -/A | | | intron-variant | AMFR | GRCh38.p7 | 16:56390910 | TAAAAAAAAAAAAAA[-/A]TGCTAGAGTTCCTTA | 267 |
| rs796783368 | in-del | -/CG | | | intron-variant | AMFR | GRCh38.p7 | 16:56365601 | GTACATACACACACA[-/CG]CACACACACGCTGGA | 267 |
| rs796796385 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56380336 | ACCCTGAGCATGACC[-/C]ACGAAACCATGTTTT | 267 |
| rs796832759 | in-del | -/ACG | | | intron-variant | AMFR | GRCh38.p7 | 16:56364434 | GAATACGCTACCAAC[-/ACG]ACAACCGTGAGTTTA | 267 |
| rs796854540 | in-del | -/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56384818 | AATTTTTTTTTTTTT[-/T]GAGACAGAGTTTCAC | 267 |
| rs796913195 | snp | C/T | | | intron-variant | AMFR | GRCh38.p7 | 16:56400224 | CACTGCAACCTCCAC[C/T]TCCCAGGTTGAAGCA | 267 |
| rs796926074 | snp | A/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374408 | CAAAGGTAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 267 |
| rs797000156 | in-del | -/C | | | intron-variant | AMFR | GRCh38.p7 | 16:56374411 | GGTAAAAAAAAAAAA[-/C]AAAAAAAAAAAACAC | 267 |