Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67250268
H2AC6
6 26135269 intron variant A/-;AA delins 4
rs9357371
MED20
6 41917581 5 prime UTR variant A/C snv 0.20 4
rs592423 6 139519556 intron variant A/C snv 0.50 3
rs3893275
LOC105374303
3 196192085 regulatory region variant A/C snv 0.13 1
rs11627546
SMOC1
14 69899207 intron variant A/C;G snv 1
rs7218708
SPECC1
17 20023523 intron variant A/C;G snv 1
rs131794
ODF3B
22 50533323 upstream gene variant A/C;G;T snv 2
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 2
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs1421312
TMPRSS6
22 37091770 intron variant A/G snv 0.45 4
rs2856646
H2AC6
6 26135270 intron variant A/G snv 0.73 4
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 3
rs7757054 6 135166476 intergenic variant A/G snv 0.13 3
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 2
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 2
rs11239550
MARCHF8
10 45529281 intron variant A/G snv 0.31 2
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs2340727 1 161976937 intergenic variant A/G snv 0.33 2
rs4657616
IFI16 ; PYDC5
1 159001296 intron variant A/G snv 0.31 2