Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 13
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs503464
CHRNA5
0.851 0.080 15 78565554 5 prime UTR variant T/A snv 0.28 6
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs11637635
CHRNA5
0.882 0.080 15 78584808 intron variant A/G snv 0.68 3
rs17408276
CHRNA5
0.882 0.080 15 78589276 non coding transcript exon variant T/C snv 0.28 3
rs3829787
CHRNA5
0.882 0.080 15 78563924 upstream gene variant C/T snv 0.27 3
rs481134
CHRNA5
0.882 0.080 15 78585221 intron variant A/G snv 0.64 3