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rs515726219

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs515726219(C;C)
Make rs515726219(C;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position67754242
GeneGNRHR
is asnp
is mentioned by
dbSNPrs515726219
ClinGenrs515726219
ebirs515726219
HLIrs515726219
Exacrs515726219
Varsomers515726219
Maprs515726219
PheGenIrs515726219
hapmaprs515726219
1000 genomesrs515726219
hgdprs515726219
ensemblrs515726219
gopubmedrs515726219
geneviewrs515726219
scholarrs515726219
googlers515726219
pharmgkbrs515726219
gwascentralrs515726219
openSNPrs515726219
23andMers515726219
23andMe allrs515726219
SNP Nexus

SNPshotrs515726219
SNPdbers515726219
MSV3drs515726219
GWAS Ctlgrs515726219
Max Magnitude0
ClinVar
Risk rs515726219(C;C)
Alt rs515726219(C;C)
Reference Rs515726219(T;T)
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.68619960T>C
CLNSRC ClinVar Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000114425.1,