Source: ALL
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: rs2231142
rs2231142
56 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 0.820 1.000 12 2008 2019
dbSNP: rs10011796
rs10011796
4 0.882 0.160 4 88169725 intron variant T/C;G snv 0.800 1.000 4 2010 2015
dbSNP: rs3775948
rs3775948
4 0.882 0.160 4 9993558 intron variant G/A;C snv 0.800 1.000 4 2010 2016
dbSNP: rs734553
rs734553
7 0.851 0.240 4 9921380 intron variant G/A;T snv 0.800 1.000 4 2010 2013
dbSNP: rs737267
rs737267
7 0.851 0.240 4 9933120 intron variant G/A;T snv 0.700 1.000 4 2008 2013
dbSNP: rs10001106
rs10001106
3 0.925 0.120 4 10125817 intergenic variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs10516200
rs10516200
3 0.925 0.120 4 10080532 intron variant C/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1071988
rs1071988
3 0.925 0.120 4 9973014 intron variant A/G;T snv 0.700 1.000 3 2010 2013
dbSNP: rs10939650
rs10939650
3 0.925 0.120 4 9996816 synonymous variant C/G;T snv 1.2E-05; 0.70 0.700 1.000 3 2010 2013
dbSNP: rs10939669
rs10939669
3 0.925 0.120 4 10044203 intron variant A/G;T snv 0.700 1.000 3 2010 2013
dbSNP: rs1109472
rs1109472
3 0.925 0.120 4 10132824 intergenic variant G/A;C;T snv 0.700 1.000 3 2010 2013
dbSNP: rs115810
rs115810
5 0.925 0.120 6 25975655 intron variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs1165205
rs1165205
4 0.925 0.120 6 25870314 intron variant T/A;G snv 0.700 1.000 3 2008 2013
dbSNP: rs11722229
rs11722229
3 0.925 0.120 4 9979073 intron variant C/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs11722930
rs11722930
3 0.925 0.120 4 10033830 intron variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs1179087
rs1179087
3 0.925 0.120 6 25858476 intron variant G/C;T snv 0.700 1.000 3 2010 2013
dbSNP: rs12501597
rs12501597
3 0.925 0.120 4 10130513 intergenic variant G/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs12502556
rs12502556
3 0.925 0.120 4 10128881 intergenic variant C/A;G snv 0.700 1.000 3 2010 2013
dbSNP: rs12505410
rs12505410
3 0.925 0.120 4 88109689 intron variant T/C;G snv 0.700 1.000 3 2010 2013
dbSNP: rs12507586
rs12507586
3 0.925 0.120 4 10146951 upstream gene variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs12508413
rs12508413
3 0.925 0.120 4 10147047 upstream gene variant G/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs13103879
rs13103879
3 0.925 0.120 4 9971255 intron variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs13115193
rs13115193
3 0.925 0.120 4 9980567 intron variant C/G;T snv 0.47 0.700 1.000 3 2010 2013
dbSNP: rs13131257
rs13131257
3 0.925 0.120 4 9980265 intron variant T/C;G snv 0.700 1.000 3 2010 2013
dbSNP: rs13145758
rs13145758
3 0.925 0.120 4 9980373 intron variant G/A;T snv 0.700 1.000 3 2010 2013