Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7328064
DGKH
1.000 0.080 13 42171982 intron variant A/C snv 0.11 1
rs7076156
ZNF365 ; LOC105378327
0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 3
rs3798519
TFAP2B
1.000 0.080 6 50821065 intron variant A/C;G snv 2
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1801197
CALCR
0.851 0.240 7 93426441 missense variant A/G snv 0.39 0.36 5
rs6123359 1.000 0.080 20 54098167 regulatory region variant A/G snv 0.12 2
rs4252402
TRPV5
1.000 0.080 7 142930043 intron variant A/G snv 0.79 1
rs6667242 1.000 0.080 1 21500073 intergenic variant A/G snv 0.16 1
rs35747824
PDILT
1.000 0.080 16 20381986 intron variant A/T snv 0.24 1
rs756322971
CASR
0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs4236481
TRPV5
1.000 0.080 7 142929678 intron variant C/A;G snv 1
rs7206790
FTO
0.925 0.160 16 53763996 intron variant C/G snv 0.49 3
rs74956940
PKN1
1.000 0.080 19 14461154 intron variant C/G snv 0.15 1
rs1126616
SPP1
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs2286526
TBX2-AS1
1.000 0.080 17 61394696 non coding transcript exon variant C/G;T snv 2
rs13006480 1.000 0.080 2 27764354 intergenic variant C/G;T snv 1
rs6928986
EPB41L2
1.000 0.080 6 131002852 intron variant C/T snv 0.78 1
rs121907896
SLC22A12
0.851 0.200 11 64591825 missense variant G/A snv 1.8E-04 8.4E-05 5
rs11746443
RGS14
0.882 0.120 5 177371305 intron variant G/A snv 0.24 0.21 4
rs1042138
CALCR
0.882 0.120 7 93426338 3 prime UTR variant G/A snv 0.15 0.11 3
rs1207568
KL
0.925 0.120 13 33016046 upstream gene variant G/A snv 0.17 3
rs4252417
TRPV5
1.000 0.080 7 142928163 synonymous variant G/A snv 5.1E-02 9.2E-02 1
rs6975977
INMT-MINDY4 ; MINDY4
1.000 0.080 7 30878216 intron variant G/A snv 7.3E-02 1
rs121907892
SLC22A12
0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13