Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 4
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 4
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 3
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 3
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 3
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 3
rs11668878
FKRP
0.925 0.200 19 46765116 intron variant G/T snv 5.1E-02 2
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 2
rs391525
IRF8
0.882 0.200 16 85910833 intron variant A/G;T snv 0.35 2
rs11688943
PPIL3
1.000 0.120 2 200875545 intron variant T/C snv 0.30 1
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 1
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 1
rs1679013 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 1
rs2003869
LEF1
0.925 0.120 4 108105258 intron variant A/C;G;T snv 1
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 1
rs2147420
FAS
1.000 0.120 10 88999856 intron variant A/G snv 0.50 1
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 1
rs2466035
PCAT1 ; CASC19
0.925 0.120 8 127198984 intron variant T/C snv 0.43 1
rs2521269
TSPAN32 ; C11orf21
0.925 0.120 11 2299865 intron variant C/A;T snv 1
rs35748167 1.000 0.120 18 60370200 intron variant G/C;T snv 1
rs3769825
CASP8
0.925 0.120 2 201246657 intron variant A/G snv 0.46 1