Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9981885 21 18958319 intron variant A/C snv 0.22 1
rs983309 8 9320222 intron variant T/G snv 0.82 2
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 3
rs895636 2 44961214 non coding transcript exon variant C/T snv 0.23 1
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 3
rs853787
ABCB11
2 168945742 intron variant G/A;T snv 2
rs853778
ABCB11
2 168954714 intron variant T/C snv 0.53 1
rs8020333
FOXN3
14 89568505 intron variant C/G;T snv 0.52 2
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs7867224
GLIS3
9 4292152 intron variant A/C;G snv 0.37 2
rs780110
IFT172
0.925 0.120 2 27462521 intron variant G/A snv 0.56 4
rs780095
GCKR
2 27518238 intron variant A/G snv 0.60 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 4
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 2
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 3
rs753993
MADD
11 47328418 non coding transcript exon variant C/A snv 0.33 2
rs749067
MADD
11 47296606 intron variant T/C snv 0.26 2
rs7173964 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 2
rs7118178
MTCH2
11 47637583 intron variant G/A snv 0.20 2
rs7101470
C11orf49
11 47032897 intron variant A/G snv 7.4E-02 2
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 1