Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10221243
rs10221243
1 17 46134944 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs10514897
rs10514897
1 17 46040031 non coding transcript exon variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10514898
rs10514898
1 17 46042270 non coding transcript exon variant A/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10514901
rs10514901
1 17 46117369 intron variant G/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10514903
rs10514903
1 17 46129280 intron variant C/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs10514904
rs10514904
1 17 46130521 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1076222
rs1076222
2 1.000 0.080 17 46032403 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1107820
rs1107820
1 17 46057993 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs11079729
rs11079729
2 1.000 0.080 17 46038203 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1117253
rs1117253
1 17 46071931 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1122380
rs1122380
1 17 46128713 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1122381
rs1122381
1 17 46128473 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150064
rs12150064
1 17 46051041 intron variant C/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150087
rs12150087
1 17 46133622 intron variant C/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150090
rs12150090
2 1.000 0.080 17 46038520 non coding transcript exon variant C/G;T snv 8.0E-06; 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150447
rs12150447
2 1.000 0.080 17 46050759 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs12150542
rs12150542
1 17 46038364 non coding transcript exon variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12185243
rs12185243
1 17 46037985 non coding transcript exon variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1468241
rs1468241
1 17 46118787 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs1476554
rs1476554
1 17 46081736 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17574228
rs17574228
3 0.925 0.120 17 46027143 3 prime UTR variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17574361
rs17574361
2 1.000 0.040 17 46030836 3 prime UTR variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17574425
rs17574425
1 17 46031822 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17574604
rs17574604
3 0.925 0.120 17 46034247 synonymous variant A/G snv 0.15 0.14 0.700 1.000 1 2012 2012
dbSNP: rs17574796
rs17574796
1 17 46037708 non coding transcript exon variant T/C snv 0.14 0.700 1.000 1 2012 2012