Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544935 0.925 0.160 6 39156672 intergenic variant T/G snv 0.18 3
rs6123359 1.000 0.080 20 54098167 regulatory region variant A/G snv 0.12 2
rs13006480 1.000 0.080 2 27764354 intergenic variant C/G;T snv 1
rs13041834 1.000 0.080 20 54086745 intergenic variant T/C snv 0.42 1
rs6667242 1.000 0.080 1 21500073 intergenic variant A/G snv 0.16 1
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 9
rs1801197
CALCR
0.851 0.240 7 93426441 missense variant A/G snv 0.39 0.36 5
rs1042138
CALCR
0.882 0.120 7 93426338 3 prime UTR variant G/A snv 0.15 0.11 3
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs756322971
CASR
0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs7328064
DGKH
1.000 0.080 13 42171982 intron variant A/C snv 0.11 1
rs6928986
EPB41L2
1.000 0.080 6 131002852 intron variant C/T snv 0.78 1
rs7206790
FTO
0.925 0.160 16 53763996 intron variant C/G snv 0.49 3
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs6975977
INMT-MINDY4 ; MINDY4
1.000 0.080 7 30878216 intron variant G/A snv 7.3E-02 1
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs9536314
KL
0.925 0.160 13 33054001 missense variant T/A;G snv 0.14 3
rs7277076
LOC105369301 ; CLDN14
1.000 0.080 21 36464675 intron variant T/C snv 0.52 2
rs35747824
PDILT
1.000 0.080 16 20381986 intron variant A/T snv 0.24 1
rs74956940
PKN1
1.000 0.080 19 14461154 intron variant C/G snv 0.15 1
rs11746443
RGS14
0.882 0.120 5 177371305 intron variant G/A snv 0.24 0.21 4
rs121907892
SLC22A12
0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs121907896
SLC22A12
0.851 0.200 11 64591825 missense variant G/A snv 1.8E-04 8.4E-05 5