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rs9658667

From SNPedia

Orientationplus
Make rs9658667(A;A)
Make rs9658667(A;G)
Make rs9658667(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position92932705
GeneCHGA
is asnp
is mentioned by
dbSNPrs9658667
ebirs9658667
HLIrs9658667
Exacrs9658667
Varsomers9658667
Maprs9658667
PheGenIrs9658667
hapmaprs9658667
1000 genomesrs9658667
hgdprs9658667
ensemblrs9658667
gopubmedrs9658667
geneviewrs9658667
scholarrs9658667
googlers9658667
pharmgkbrs9658667
gwascentralrs9658667
openSNPrs9658667
23andMers9658667
23andMe allrs9658667
SNP Nexus

SNPshotrs9658667
SNPdbers9658667
MSV3drs9658667
GWAS Ctlgrs9658667
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 26556564] Analysis and validation of traits associated with a single nucleotide polymorphism Gly364Ser in catestatin using humanized chromogranin A mouse models