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
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
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
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10