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rs797044452

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044452(A;A)
Make rs797044452(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position67744788
GeneGNRHR
is asnp
is mentioned by
dbSNPrs797044452
ebirs797044452
HLIrs797044452
Exacrs797044452
Varsomers797044452
Maprs797044452
PheGenIrs797044452
hapmaprs797044452
1000 genomesrs797044452
hgdprs797044452
ensemblrs797044452
gopubmedrs797044452
geneviewrs797044452
scholarrs797044452
googlers797044452
pharmgkbrs797044452
gwascentralrs797044452
openSNPrs797044452
23andMers797044452
23andMe allrs797044452
SNP Nexus

SNPshotrs797044452
SNPdbers797044452
MSV3drs797044452
GWAS Ctlgrs797044452
Max Magnitude0
ClinVar
Risk rs797044452(A;A)
Alt rs797044452(A;A)
Reference rs797044452(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 1
HGVS NC_000004.11:g.68610506C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030917.29,