Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs12445050
PLCG2
16 81837364 intron variant C/T snv 9.6E-02 3
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs5758896
A4GALT
22 42719570 intron variant T/C snv 0.55 3
rs6088735
MMP24-AS1-EDEM2
20 35157873 intergenic variant C/T snv 0.25 3
rs643434
ABO
9 133266942 intron variant A/G;T snv 3
rs9390460
STXBP5
6 147373198 intron variant T/C snv 0.51 3
rs10498632
TC2N
14 91824400 intron variant A/G snv 0.29 2
rs13044899
NCOA6
20 34699274 intron variant G/A snv 0.41 2
rs1409338
PLXDC2
10 19938338 intron variant A/G snv 0.75 2
rs28446901
ADAMTS13
9 133443675 intron variant C/G snv 0.18 2
rs3002416 X 39850941 upstream gene variant C/T snv 0.33 2
rs4253417
F11
4 186277851 intron variant T/C;G snv 2
rs4253421
F11
4 186283783 intron variant A/C;G;T snv 2
rs4734879
ZFPM2-AS1 ; ZFPM2
8 105570896 intron variant A/G snv 0.31 2
rs9411377
ABO
9 133269992 intron variant A/C snv 0.62 2
rs10090114
MSRA
8 10147444 intron variant T/C snv 0.90 1
rs1018827
F5
1 169544768 intron variant A/G snv 0.92 1
rs1021230
EBF2
8 25928927 intron variant A/T snv 0.27 1
rs1048483
SMG6 ; HIC1
17 2063163 3 prime UTR variant C/T snv 0.43 1
rs10746487 1 9278630 intergenic variant T/A;C snv 1
rs10747514
PROCR ; MMP24-AS1-EDEM2
20 35187566 intron variant G/A snv 0.40 1
rs10919507 1 170885468 intron variant C/T snv 3.0E-02 1
rs11057270
SBNO1
12 123323526 intron variant T/C snv 0.28 1
rs11158204
LOC105370522
14 58377808 intron variant C/T snv 0.25 1