Gene: CHRNB3 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13280604
rs13280604
CHRNB3 ; LOC105379396
7 0.851 0.160 8 42704443 5 prime UTR variant G/A snv 0.62 0.700 1.000 1 2010 2010
dbSNP: rs1530848
rs1530848
CHRNB3 ; LOC105379396
1 8 42697765 intron variant G/T snv 0.60 0.700 1.000 1 2010 2010
dbSNP: rs16891561
rs16891561
CHRNB3
1 8 42724596 intron variant T/C snv 0.60 0.700 1.000 1 2010 2010
dbSNP: rs6474414
rs6474414
CHRNB3
1 8 42705193 intron variant A/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs6474415
rs6474415
CHRNB3
1 8 42707795 intron variant G/A snv 0.60 0.700 1.000 1 2010 2010
dbSNP: rs6997909
rs6997909
CHRNB3 ; LOC105379396
1 8 42705106 intron variant A/G snv 0.60 0.700 1.000 1 2010 2010
dbSNP: rs7004381
rs7004381
CHRNB3 ; LOC105379396
1 8 42696018 upstream gene variant A/C;G snv 0.700 1.000 1 2010 2010