Source: GWASCAT ×
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 24
rs35747
LOC105369944
12 102518780 intergenic variant G/A snv 0.70 3
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 10
rs2967951
LOC105369214 ; ROPN1L
5 10463995 intron variant C/T snv 0.19 1
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 1
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs308971
SYN2
3 12075120 intron variant G/A snv 0.82 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs7973683
CCDC92
12 123964676 intron variant C/A snv 0.39 1
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 1
rs867559 9 126703046 non coding transcript exon variant A/G snv 0.26 1
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 3
rs2275215
LOC102723409
6 129540247 intron variant T/C snv 0.35 1
rs1542829
COL6A5
3 130418627 intron variant G/A snv 8.0E-02 1
rs1106683 7 131768766 intergenic variant G/A snv 0.14 1
rs2890652 2 142202362 intergenic variant T/C snv 0.21 1
rs7708584
MFAP3
5 154163906 intron variant A/G snv 0.58 1
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs516636 1 177886382 intron variant C/A snv 0.17 1
rs574367 1 177904075 intron variant G/T snv 0.16 1
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 1