Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 30
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 19
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 18
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 12
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10