Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs762679
MCM4
8 47972876 missense variant T/A snv 0.87 0.88 4
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs4936675
PPP2R1B
11 111752364 intron variant T/A snv 0.71 0.75 1
rs2243558
NIBAN2
9 127527336 intron variant C/A;G;T snv 2.4E-05; 0.63 1
rs470119
TYMP
22 50528485 non coding transcript exon variant T/C;G snv 0.61; 8.2E-06 2
rs8012
SYCE2 ; GCDH
19 12899706 3 prime UTR variant A/G snv 0.61 0.64 2
rs131804
TYMP ; SCO2
22 50526433 missense variant G/A snv 0.61 0.51 1
rs11042023
TRIM66
1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 3
rs1134634
CC2D2A
4 15601446 3 prime UTR variant G/C;T snv 0.58; 9.4E-06 2
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs8432
BBS1 ; ZDHHC24
11 66532044 3 prime UTR variant A/G snv 0.55 0.66 1
rs2227930
ATR
3 142558733 synonymous variant A/T snv 0.55 0.63 2
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs6532835
LAMTOR3
4 99884050 intron variant C/A snv 0.47 0.54 1
rs11671654
ZNF69
19 11903540 intron variant C/G snv 0.46 0.37 1
rs13006529
CASP10
0.851 0.080 2 201217736 missense variant T/A snv 0.41 0.42 1
rs1064351
HOMER3 ; HOMER3-AS1
19 18938389 synonymous variant G/A snv 0.40 0.34 1
rs7193541
RFWD3
1.000 0.160 16 74630845 missense variant T/C snv 0.37 0.43 2
rs595982
PPP1R15A
19 48874988 synonymous variant T/C snv 0.33 0.39 3
rs2072153
ZNF652
17 49312652 intron variant G/A;C snv 3.7E-04; 0.33 2
rs11135695
LOC286059 ; TNFRSF10B
8 23068985 5 prime UTR variant G/A;C snv 0.33; 4.4E-06 1
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