Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs2967951
LOC105369214 ; ROPN1L
5 10463995 intron variant C/T snv 0.19 2
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 2
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs7001819
LOC105379243
0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 2
rs308971
SYN2
3 12075120 intron variant G/A snv 0.82 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs7973683
CCDC92
12 123964676 intron variant C/A snv 0.39 2
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 2
rs146199292
OSBPL11
3 125594708 missense variant G/T snv 2.0E-05 5.6E-05 2
rs867559 9 126703046 non coding transcript exon variant A/G snv 0.26 2
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 2
rs2275215
LOC102723409
6 129540247 intron variant T/C snv 0.35 2
rs1542829
COL6A5
3 130418627 intron variant G/A snv 8.0E-02 2
rs1106683 7 131768766 intergenic variant G/A snv 0.14 2
rs146922831
LRGUK
7 134201557 missense variant G/T snv 3.2E-05 2.0E-04 2
rs2890652 2 142202362 intergenic variant T/C snv 0.21 2
rs200861231
FREM1
9 14859403 missense variant C/A;T snv 5.2E-05 2.8E-05 2
rs7708584
MFAP3
5 154163906 intron variant A/G snv 0.58 2
rs34572584 4 170869381 intergenic variant G/T snv 3.3E-02 2
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs516636 1 177886382 intron variant C/A snv 0.17 2
rs574367 1 177904075 intron variant G/T snv 0.16 2