Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801020
GRK6 ; F12 ; SLC34A1
1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 3
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 3
rs2545801
GRK6
5 177414338 intron variant T/C snv 0.56 3
rs2469184
AGBL1
15 86648746 intron variant A/G snv 0.54 1
rs710446
KNG1
0.925 0.120 3 186742138 missense variant T/C snv 0.42 0.44 1
rs266723
KNG1
3 186729258 intron variant A/C snv 0.44 1
rs9898
HRG ; LOC105374258
0.925 0.160 3 186672838 missense variant C/T snv 0.38 0.43 2
rs5030091
KNG1
3 186743088 3 prime UTR variant T/C snv 0.42 1
rs1624230
KNG1
3 186721146 intron variant C/A snv 0.42 1
rs1624569
KNG1
3 186732280 intron variant T/C snv 0.38 1
rs2304595
KLKB1
1.000 0.040 4 186251126 non coding transcript exon variant G/A snv 0.36 1
rs4253304
KLKB1
4 186252417 intron variant G/C snv 0.36 1
rs2050190
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32371299 intron variant A/G snv 0.35 2
rs5030062
KNG1
3 186736391 non coding transcript exon variant A/C snv 0.35 1
rs2289252
F11-AS1 ; F11
1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35 2
rs1621816
KNG1
3 186721384 non coding transcript exon variant T/C snv 0.32 1
rs3856930
KNG1
3 186740533 intron variant C/T snv 0.27 1
rs12644950 4 154616169 upstream gene variant G/A snv 0.25 2
rs5030028
KNG1
3 186727965 intron variant C/T snv 0.23 1
rs6028
F5
1 169582444 synonymous variant T/C snv 0.29 0.23 1
rs5030023
KNG1
3 186726855 intron variant G/A snv 0.20 1
rs2062632
KNG1
3 186743392 3 prime UTR variant T/C snv 0.19 1
rs13177732
GRK6
5 177429924 intron variant T/G snv 0.16 1
rs7381103
GRK6 ; SLC34A1 ; F12
5 177411311 intron variant C/G snv 0.11 1
rs2287694
GRK6
5 177433292 intron variant T/C snv 8.5E-02 2