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rs10483774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10483774(A;A)
Make rs10483774(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position64296881
GeneESR2
is asnp
is mentioned by
dbSNPrs10483774
dbSNP (classic)rs10483774
ClinGenrs10483774
ebirs10483774
HLIrs10483774
Exacrs10483774
Gnomadrs10483774
Varsomers10483774
LitVarrs10483774
Maprs10483774
PheGenIrs10483774
Biobankrs10483774
1000 genomesrs10483774
hgdprs10483774
ensemblrs10483774
geneviewrs10483774
scholarrs10483774
googlers10483774
pharmgkbrs10483774
gwascentralrs10483774
openSNPrs10483774
23andMers10483774
SNPshotrs10483774
SNPdbers10483774
MSV3drs10483774
GWAS Ctlgrs10483774
GMAF0.04591
Max Magnitude0
? (A;A) (A;G) (G;G) 28


OMIM601663
DescESTROGEN RECEPTOR 2; ESR2
Variant
Relatedalso

[PMID 17579196] Risk factors for hypospadias in the estrogen receptor 2 gene.

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