Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25