Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 2
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 2
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 2
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 2
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 1
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs965469
C20orf194
1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 1
rs11697186
DDRGK1
1.000 0.080 20 3204477 intron variant A/C;T snv 7.0E-02 1