Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4549631 6 126645162 intron variant T/C;G snv 2
rs7846385 8 77247943 intergenic variant T/C snv 0.23 2
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs4272
CDK6
1.000 0.120 7 92607515 3 prime UTR variant A/G;T snv 2
rs12982744
DOT1L
0.925 0.040 19 2177194 intron variant C/A;G;T snv 2
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 2
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs314268
LIN28B
6 104970103 intron variant G/A snv 0.64 2
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 2
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 2
rs4337252
LOXL1
1.000 0.040 15 73934424 intron variant G/C snv 0.52 2
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 2
rs12145922
PKN2-AS1
1 88680551 intron variant C/A snv 0.57 2
rs879882
POU5F1
1.000 0.160 6 31171675 intron variant T/C;G snv 2
rs1344674
ZBTB38
3 141406344 intron variant A/G snv 0.55 2
rs1991431
ZBTB38
3 141414608 intron variant G/A snv 0.50 2
rs2871960
ZBTB38
3 141402972 5 prime UTR variant A/C snv 0.55 2
rs6763931
ZBTB38
0.925 0.080 3 141383991 intron variant G/A snv 0.54 2
rs1013209 8 24258791 intergenic variant C/T snv 0.28 1
rs10231759 7 150815084 regulatory region variant T/C snv 0.41 1
rs10472828 5 32888712 non coding transcript exon variant C/T snv 0.40 1
rs1052483 2 219069626 non coding transcript exon variant G/T snv 0.13 1
rs10748128 12 69433878 intergenic variant G/T snv 0.42 1