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rs13138607

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs13138607(A;A)
Make rs13138607(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position67755832
GeneGNRHR
is asnp
is mentioned by
dbSNPrs13138607
dbSNP (classic)rs13138607
ClinGenrs13138607
ebirs13138607
HLIrs13138607
Exacrs13138607
Gnomadrs13138607
Varsomers13138607
LitVarrs13138607
Maprs13138607
PheGenIrs13138607
Biobankrs13138607
1000 genomesrs13138607
hgdprs13138607
ensemblrs13138607
geneviewrs13138607
scholarrs13138607
googlers13138607
pharmgkbrs13138607
gwascentralrs13138607
openSNPrs13138607
23andMers13138607
SNPshotrs13138607
SNPdbers13138607
MSV3drs13138607
GWAS Ctlgrs13138607
GMAF0.4536
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22710726] Single nucleotide polymorphisms in the regulatory region of gonadotropin-releasing hormone receptor gene and breast cancer susceptibility


[PMID 19640273OA-icon.png] Genetic polymorphisms of the GNRH1 and GNRHR genes and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).


ClinVar
Risk rs13138607(A;A)
Alt rs13138607(A;A)
Reference Rs13138607(G;G)
Significance Probable-non-pathogenic
Disease Isolated GnRH Deficiency
Variation info
Gene GNRHR
CLNDBN Isolated GnRH Deficiency
Reversed 0
HGVS NC_000004.11:g.68621550G>A
CLNSRC
CLNACC RCV000291948.1,