Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs2908004
WNT16
1.000 0.040 7 121329715 missense variant G/A;T snv 0.44; 4.0E-06 4
rs3755955
IDUA
0.925 0.080 4 1000626 missense variant G/A;C snv 0.16; 8.0E-06 4
rs6831280
IDUA
0.925 0.080 4 1002377 missense variant G/A;C snv 0.17 4
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 3
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 3
rs2016266
SP7
1.000 0.080 12 53334171 intron variant G/A;C snv 3
rs6913578 0.925 0.080 6 151628671 intergenic variant A/C;T snv 3
rs10226308
EPDR1 ; NME8
7 37898820 intron variant A/C;G snv 2
rs10876432
SP7
12 53338107 intron variant G/A snv 2
rs118115924
LOC105369757
12 48985754 downstream gene variant G/A;T snv 2
rs1262476
LOC105377992
6 126665850 intron variant A/G;T snv 2
rs12741884 1 22268202 downstream gene variant G/A;C snv 2
rs12742784 1.000 0.080 1 22355873 intergenic variant C/A;T snv 2
rs13204965 6 126845927 intron variant A/C;T snv 2
rs1346004 2 165744536 downstream gene variant G/A;T snv 2
rs13469
POLDIP2
17 28349109 synonymous variant C/G;T snv 0.53 2
rs1471403 1.000 0.080 4 87854091 intergenic variant T/A;C snv 2
rs1871859
CCDC170
6 151577371 intron variant C/G;T snv 2
rs1905786
TNFRSF11B
1.000 0.040 8 118939453 intron variant T/A;C snv 2
rs227425
SMOC1
14 69989982 intron variant T/A;G snv 2