Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11263654 1.000 0.120 11 69423355 upstream gene variant C/T snv 0.11 1
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 1
rs13376700 1.000 0.120 1 51011971 intergenic variant T/A snv 0.48 1
rs7765284 1.000 0.120 6 85068104 intergenic variant C/A snv 0.13 1
rs78971134 1.000 0.120 12 107258753 intergenic variant A/G snv 7.7E-02 1
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs7913447
ANAPC16
1.000 0.120 10 72232282 intron variant C/A;T snv 1
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs375129361
BAP1
0.925 0.120 3 52408056 missense variant T/A;C snv 4.1E-06 1
rs3206824
DKK3
0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 1
rs4903064
DPF3
0.925 0.120 14 72812712 intron variant T/C snv 0.23 1
rs1057519973
ELOC
1.000 0.120 8 73946733 missense variant T/A;G snv 1
rs1057519974
ELOC
1.000 0.120 8 73946734 missense variant A/T snv 1
rs10211665
EPAS1
1.000 0.120 2 46298957 intron variant T/C snv 0.58 1
rs11125068
EPAS1
1.000 0.120 2 46300677 intron variant A/G snv 0.62 1
rs11684885
EPAS1
1.000 0.120 2 46306413 intron variant T/C;G snv 1
rs17034950
EPAS1
1.000 0.120 2 46311655 intron variant G/A snv 0.25 1
rs1867784
EPAS1
1.000 0.120 2 46307081 intron variant T/C snv 0.40 1
rs1867785
EPAS1
1.000 0.120 2 46307199 intron variant A/G snv 0.52 1
rs1867787
EPAS1
1.000 0.120 2 46298252 intron variant G/C;T snv 1
rs2034327
EPAS1
1.000 0.120 2 46321901 intron variant G/C snv 0.59 1
rs2044456
EPAS1
1.000 0.120 2 46319177 intron variant A/G snv 0.26 1
rs2121266
EPAS1
1.000 0.120 2 46308785 intron variant C/A snv 0.61 1
rs2346417
EPAS1
1.000 0.120 2 46301822 intron variant T/A snv 0.39 1
rs4952818
EPAS1
1.000 0.120 2 46309917 intron variant C/T snv 0.39 1