Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1451724
RHOG
1.000 0.080 11 3835438 intron variant G/A snv 0.39 1
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs1475839
KCNJ6
1.000 0.080 21 37649639 intron variant C/T snv 0.31 3
rs1515050
KCNJ6
1.000 0.080 21 37630840 intron variant T/C snv 0.75 3
rs1515056
LOC107985507 ; KCNJ6
1.000 0.080 21 37710283 intron variant C/G;T snv 0.28 3
rs1612735
ADH1B ; ADH1C
1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1614972
ADH1B ; ADH1C
0.925 0.160 4 99336998 intron variant C/T snv 0.38 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81 3
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
rs17028719 1.000 0.080 1 5734948 intergenic variant A/G snv 4.8E-02 1
rs1709817
KCNJ6
1.000 0.080 21 37664047 intron variant T/A;C snv 3
rs1709818
KCNJ6
1.000 0.080 21 37663909 intron variant T/C snv 0.57 3
rs1709819
KCNJ6
1.000 0.080 21 37663813 intron variant A/C snv 0.59 3
rs1709820
KCNJ6
1.000 0.080 21 37663669 intron variant A/C snv 0.57 3
rs1709826
KCNJ6
1.000 0.080 21 37677171 intron variant G/A;C snv 3
rs1709832
KCNJ6
1.000 0.080 21 37665865 intron variant T/G snv 0.57 3
rs1709833
KCNJ6
1.000 0.080 21 37665503 intron variant A/G snv 0.57 3
rs1709835
KCNJ6
1.000 0.080 21 37665334 intron variant A/C;G snv 0.57 3
rs17125651 1.000 0.080 10 109063325 intergenic variant T/C snv 0.14 3
rs17536732
FSTL5
1.000 0.080 4 161903214 intron variant G/T snv 4.7E-02 3
rs17616845 1.000 0.080 7 12741918 intron variant T/C snv 0.15 1
rs17754467
NRXN3
1.000 0.080 14 78156180 intergenic variant A/G snv 0.18 1
rs17814920
KCNJ6
1.000 0.080 21 37643595 intron variant G/A snv 0.27 3