rs16862847

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs16862847(A;G)

Make rs16862847(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

174764872

Gene

CHRNA1

is a	snp
is	mentioned by
dbSNP	rs16862847
dbSNP (classic)	rs16862847
ClinGen	rs16862847
ebi	rs16862847
HLI	rs16862847
Exac	rs16862847
Gnomad	rs16862847
Varsome	rs16862847
LitVar	rs16862847
Map	rs16862847
PheGenI	rs16862847
Biobank	rs16862847
1000 genomes	rs16862847
hgdp	rs16862847
ensembl	rs16862847
geneview	rs16862847
scholar	rs16862847
google	rs16862847
pharmgkb	rs16862847
gwascentral	rs16862847
openSNP	rs16862847
23andMe	rs16862847
SNPshot	rs16862847
SNPdbe	rs16862847
MSV3d	rs16862847
GWAS Ctlg	rs16862847

GMAF

0.1093

Max Magnitude

0

OMIM	100690
Desc	CHOLINERGIC RECEPTOR, NICOTINIC, ALPHA POLYPEPTIDE 1; CHRNA1
Variant
Related	also

ClinVar
Risk	rs16862847(G;G)
Alt	rs16862847(G;G)
Reference	Rs16862847(A;A)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	CHRNA1
CLNDBN	not specified
Reversed	1
HGVS	NC_000002.11:g.175629600T>C
CLNSRC
CLNACC	RCV000249329.1,