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rs10009228

From SNPedia

Orientationplus
Stabilizedplus
Make rs10009228(A;A)
Make rs10009228(A;G)
Make rs10009228(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position40354405
GeneCHRNA9
is asnp
is mentioned by
dbSNPrs10009228
ebirs10009228
HLIrs10009228
Exacrs10009228
Varsomers10009228
Maprs10009228
PheGenIrs10009228
hapmaprs10009228
1000 genomesrs10009228
hgdprs10009228
ensemblrs10009228
gopubmedrs10009228
geneviewrs10009228
scholarrs10009228
googlers10009228
pharmgkbrs10009228
gwascentralrs10009228
openSNPrs10009228
23andMers10009228
23andMe allrs10009228
SNP Nexus

SNPshotrs10009228
SNPdbers10009228
MSV3drs10009228
GWAS Ctlgrs10009228
GMAF0.242
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22125646OA-icon.png] Naturally occurring variants of human ?9 nicotinic receptor differentially affect bronchial cell proliferation and transformation


[PMID 22406075OA-icon.png] Association of single nucleotide polymorphisms of nicotinic acetylcholine receptor subunits with cervical neoplasia


GET Evidence
CHRNA9-N442S
aa_change Asn442Ser
aa_change_short N442S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.76873
summary