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: rs2832407
rs2832407
2 0.925 0.080 21 29595188 intron variant C/A;T snv 0.040 1.000 4 2014 2014
dbSNP: rs13273672
rs13273672
2 0.925 0.080 8 11754872 intron variant T/C snv 0.34 0.010 1.000 1 2016 2016
dbSNP: rs141696414
rs141696414
1 1.000 12 111783258 missense variant G/A;T snv 9.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2019 2019
dbSNP: rs1876831
rs1876831
4 0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 0.010 1.000 1 2008 2008
dbSNP: rs2073478
rs2073478
2 0.925 0.040 9 38396068 missense variant G/A;T snv 2.0E-05; 0.51 0.010 1.000 1 2014 2014
dbSNP: rs3027172
rs3027172
2 0.925 0.080 17 8152405 missense variant A/G snv 0.38 0.17 0.010 1.000 1 2011 2011