Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2836441
ERG
21 38498386 5 prime UTR variant G/A snv 0.87 0.89 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 1
rs513349
GGNBP1 ; BAK1
1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 1
rs2932536
CAPZA1
1 112659795 intron variant G/A snv 0.50 0.51 1
rs2235989
DDO
6 110393381 intron variant A/T snv 0.45 0.47 1
rs41315846
GCSAML
1 247549001 intron variant T/C snv 0.44 0.52 3
rs7833924
PLEC
8 143921861 missense variant A/G snv 0.40 0.53 1
rs399604
HLA-DOA
1.000 0.120 6 33007237 non coding transcript exon variant T/C snv 0.40 0.40 1
rs8073060
SLFN14 ; LOC107985032
17 35548243 missense variant T/A snv 0.32 0.34 3
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs2297067
EXOC3L4
1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 2
rs10512472
SLFN14
17 35557785 missense variant T/C snv 0.21 0.19 1
rs9462031
UHRF1BP1
6 34863984 intron variant G/T snv 0.19 0.23 1
rs7811142
TSC22D4
7 100467820 synonymous variant A/C;T snv 0.16 1
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs151233
CLN3 ; APOBR
16 28495107 synonymous variant C/T snv 0.14 0.13 2
rs1704413
PLA2G4E-AS1 ; EHD4
15 41972233 intron variant A/G snv 0.13 0.17 1
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 1
rs75501914
LOC105374354 ; HGFAC
4 3448054 intron variant G/A snv 7.9E-02 5.6E-02 2