Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 19
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 17
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 17
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 17