Have questions? Visit https://www.reddit.com/r/SNPedia

rs16862847

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs16862847(A;G)
Make rs16862847(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position174764872
GeneCHRNA1
is asnp
is mentioned by
dbSNPrs16862847
dbSNP (old)rs16862847
ClinGenrs16862847
ebirs16862847
HLIrs16862847
Exacrs16862847
Gnomadrs16862847
Varsomers16862847
Maprs16862847
PheGenIrs16862847
Biobankrs16862847
1000 genomesrs16862847
hgdprs16862847
ensemblrs16862847
gopubmedrs16862847
geneviewrs16862847
scholarrs16862847
googlers16862847
pharmgkbrs16862847
gwascentralrs16862847
openSNPrs16862847
23andMers16862847
23andMe allrs16862847
SNP Nexus

SNPshotrs16862847
SNPdbers16862847
MSV3drs16862847
GWAS Ctlgrs16862847
GMAF0.1093
Max Magnitude0
OMIM100690
DescCHOLINERGIC RECEPTOR, NICOTINIC, ALPHA POLYPEPTIDE 1; CHRNA1
Variant
Relatedalso


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,