Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 5
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs13077101
RABL3
3 120706484 intron variant T/C snv 3
rs139761834
CD36
7 80545045 intron variant T/C snv 2.8E-04 3
rs16840760 2 204118831 intergenic variant T/C snv 3.6E-02 3
rs1818782
DAB2 ; C9
5 39424526 intron variant A/C snv 0.56 3
rs2078087
NMNAT2
1 183389270 intron variant C/T snv 0.16 3
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv 3
rs34010237
FCGRT
19 49509317 intron variant G/A snv 0.13 3
rs4949718
ST6GALNAC3
1 76433779 intron variant T/A;C snv 3
rs74913549
PANX1
11 94180526 intron variant T/A;C snv 3
rs75759936 4 78698045 intergenic variant C/A snv 5.0E-03 3
rs892295
CHL1
3 355870 intron variant A/G snv 0.87 3
rs11067592 12 109631385 intergenic variant G/T snv 1.2E-03 2
rs4598207 7 50218883 intron variant A/T snv 0.34 2
rs10165093
EFHD1
2 232639279 intron variant G/A snv 0.41 1
rs10198552
ACMSD ; CCNT2-AS1
2 134842306 intron variant T/C snv 6.2E-02 1
rs10509735
CNNM1
10 99372525 intron variant A/C snv 0.56 1
rs10827785 10 17933413 intergenic variant T/C snv 0.25 1
rs11292716
PON1
7 95305887 intron variant A/- delins 1
rs114059064 6 33108491 upstream gene variant T/C snv 1