Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9974023
RALY
20 34051022 intron variant A/C;G snv 2
rs17309872
ACSS2 ; GSS
0.925 0.080 20 34927985 downstream gene variant A/C;G;T snv 2
rs2378332
TRPC4AP
20 35029447 intron variant A/C;G;T snv 2
rs6088521
MAP1LC3A
20 34545380 upstream gene variant A/C;G;T snv 2
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs11906318
MMP24-AS1-EDEM2 ; EDEM2
20 35141639 intron variant A/C;T snv 2
rs2425047
FAM83C-AS1 ; EIF6
20 35283872 intron variant A/C;T snv 2
rs334144
IWS1
2 127502081 intron variant A/C;T snv 2
rs6119535
GGT7
20 34854335 intron variant A/C;T snv 2
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs1178977
BAZ1B
0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21 5
rs12478841
ZNF512
0.925 0.120 2 27588855 intron variant A/G snv 0.27 5
rs2384656
ZNF512
0.925 0.120 2 27609188 intron variant A/G snv 0.27 5
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 5
rs867186
PROCR ; MMP24-AS1-EDEM2
0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 5
rs2295888
EDEM2 ; MMP24-AS1-EDEM2
20 35135060 intron variant A/G snv 0.14 3
rs6088692
TRPC4AP
1.000 0.080 20 35050785 intron variant A/G snv 0.58 3
rs1040552 20 33861523 regulatory region variant A/G snv 0.19 2
rs11683427
CYP27C1
2 127198967 intron variant A/G snv 0.22 2
rs11691088
MAP3K2
2 127374277 non coding transcript exon variant A/G snv 0.27 2
rs11907022
NFS1
20 35695704 intron variant A/G snv 0.10 2
rs11908470
SCAND1 ; CNBD2
20 35957141 intron variant A/G snv 8.2E-02 2
rs12480555
ASIP
20 34196688 intron variant A/G snv 0.11 2
rs13041173 20 33955008 intergenic variant A/G snv 0.25 2