Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs11814448 0.925 0.080 10 22026914 intergenic variant A/C snv 0.21 1
rs3734805
CCDC170 ; LOC107986528
0.925 0.080 6 151618215 3 prime UTR variant A/C snv 6.9E-02 1
rs6180
GHR
0.827 0.160 5 42719137 missense variant A/C snv 0.44 0.43 1
rs6815814
TLR1
1.000 0.080 4 38814717 intron variant A/C snv 0.43 1
rs9693444 0.925 0.080 8 29652100 intergenic variant A/C snv 0.66 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 2
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs7107217 0.882 0.160 11 129603795 intron variant A/C;G snv 2
rs11196174
TCF7L2
1.000 0.080 10 112974337 intron variant A/C;G snv 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs2543519
TMPRSS6
0.925 0.080 22 37084229 missense variant A/C;G snv 0.22 1
rs12906542
ADAMTS7P3
0.925 0.080 15 77977130 intron variant A/C;G;T snv 1
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 2
rs1316170
RAD51B
1.000 0.080 14 68231755 intron variant A/C;T snv 1
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 1
rs6913578 0.925 0.080 6 151628671 intergenic variant A/C;T snv 1
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 1
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3