Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011019
ERCC3
2 127279984 intron variant A/G;T snv 0.75 2
rs1018503
NCOA6
20 34737712 intron variant T/A;G snv 2
rs1019842
MYO7B
2 127547621 intron variant T/C snv 0.86 2
rs10208529
C2orf16
0.925 0.120 2 27563321 intron variant A/T snv 0.28 5
rs1033797
MMP24-AS1-EDEM2 ; EDEM2
20 35131884 intron variant T/C snv 0.27 2
rs1033799
EDEM2 ; MMP24-AS1-EDEM2
20 35132230 intron variant C/A snv 0.17 2
rs1040552 20 33861523 regulatory region variant A/G snv 0.19 2
rs10485505
ITCH
1.000 0.080 20 34437762 intron variant C/G;T snv 2
rs10485508
TRPC4AP
20 35017295 intron variant C/T snv 8.0E-02 2
rs10496661
MAP3K2
2 127332568 intron variant G/T snv 0.24 2
rs1058003
TRPC4AP ; MYH7B
20 35002614 3 prime UTR variant G/A snv 0.58 2
rs10803588
LOC105373609 ; MYO7B
2 127570800 intron variant C/T snv 0.37 2
rs10875492
TRPC4AP
20 35043604 intron variant C/T snv 0.58 2
rs10928772
MYO7B
2 127584028 intron variant T/G snv 0.35 2
rs11167260
PROCR ; MMP24-AS1-EDEM2
20 35187397 intron variant G/A snv 9.1E-02 2
rs1124511
EDEM2 ; MMP24-AS1-EDEM2
20 35148894 upstream gene variant A/C snv 0.48 2
rs1158867
PROC
1.000 0.080 2 127419801 splice region variant C/T snv 0.51 3
rs1160297
LOC105369165
2 53010182 intergenic variant G/C snv 0.69 2
rs11679414
MAP3K2-DT
2 127393427 intron variant G/A snv 0.27 2
rs11680949
MAP3K2
2 127365986 intron variant C/G snv 0.25 2
rs11683427
CYP27C1
2 127198967 intron variant A/G snv 0.22 2
rs11683986
IWS1 ; LOC105373608
2 127438822 intron variant C/T snv 0.28 2
rs11691088
MAP3K2
2 127374277 non coding transcript exon variant A/G snv 0.27 2
rs11696652
TRPC4AP
20 35049257 intron variant T/G snv 0.19 2
rs11696967
MMP24-AS1-EDEM2
20 35155806 intergenic variant A/C snv 0.23 2