Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1876831
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 4
rs2073478
ALDH1B1
0.925 0.040 9 38396068 missense variant G/A;T snv 2.0E-05; 0.51 2
rs13273672
GATA4
0.925 0.080 8 11754872 intron variant T/C snv 0.34 2
rs2832407
GRIK1 ; GRIK1-AS2 ; BACH1
0.925 0.080 21 29595188 intron variant C/A;T snv 2
rs3027172
PER1
0.925 0.080 17 8152405 missense variant A/G snv 0.38 0.17 2
rs141696414
ALDH2
1.000 12 111783258 missense variant G/A;T snv 9.2E-05 1