Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 4
rs10799590
CNIH3
1 224634780 intron variant G/A snv 0.56 1