Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 4
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 3
rs419076
MECOM
3 169383098 intron variant T/A;C snv 3
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 3
rs1717027
ULK4
1.000 0.160 3 41946428 intron variant T/A;C snv 2
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 2
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 2
rs11160059
SLC24A4
14 92340986 intron variant T/A;C snv 1
rs12098941 11 55898967 downstream gene variant T/A;G snv 1
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 1
rs13149993 4 80237391 regulatory region variant G/A;C snv 1
rs1401454
SOX6
11 16228637 intron variant C/A;G;T snv 1
rs1421811
NPR3
5 32714164 intron variant C/G;T snv 1
rs1492840 4 45764988 intergenic variant A/C;G;T snv 1
rs16877320 6 15922795 TF binding site variant T/A;C snv 1
rs17511601
OR5W2
11 55913899 missense variant T/C;G snv 1.6E-05; 6.1E-02 1
rs17527788
OR7E5P
11 55979537 non coding transcript exon variant C/G;T snv 6.9E-06; 5.9E-02 1