Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs10483038
KCNJ6
1.000 0.080 21 37652469 intron variant T/C snv 0.26 3
rs11075992
FTO
1.000 0.080 16 53786154 intron variant T/C snv 0.41 3
rs111372083
KCNJ6
1.000 0.080 21 37638374 intron variant C/A;T snv 0.27 3
rs111576572
KCNJ6
1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32 3
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs115460205
FSTL5
1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 3
rs12482570
LOC107985507 ; KCNJ6
1.000 0.080 21 37705475 intron variant A/G snv 0.30 3
rs12639833
ADH1C ; ADH1B
1.000 0.080 4 99346215 intron variant C/T snv 0.31 3
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs1316543
GRK5
1.000 0.080 10 119445148 intron variant G/A snv 0.15 3
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3