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rs369176613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369176613(A;A)
Make rs369176613(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position67740661
GeneGNRHR
is asnp
is mentioned by
dbSNPrs369176613
ebirs369176613
HLIrs369176613
Exacrs369176613
Varsomers369176613
Maprs369176613
PheGenIrs369176613
hapmaprs369176613
1000 genomesrs369176613
hgdprs369176613
ensemblrs369176613
gopubmedrs369176613
geneviewrs369176613
scholarrs369176613
googlers369176613
pharmgkbrs369176613
gwascentralrs369176613
openSNPrs369176613
23andMers369176613
23andMe allrs369176613
SNP Nexus

SNPshotrs369176613
SNPdbers369176613
MSV3drs369176613
GWAS Ctlgrs369176613
Max Magnitude0
ClinVar
Risk rs369176613(A;A)
Alt rs369176613(A;A)
Reference rs369176613(G;G)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 7 with or without anosmia
Variation info
Gene GNRHR
CLNDBN Hypogonadotropic hypogonadism 7 with or without anosmia
Reversed 0
HGVS NC_000004.11:g.68606379G>A
CLNSRC ClinVar Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000128827.1, RCV000203470.1,