Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs113809617
TMEM203 ; NDOR1
9 137205865 missense variant C/G snv 0.13 0.12 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5