Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 1
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 1
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 4
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 3
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 2
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 1
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 2