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rs515726220

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726220(A;A)
Make rs515726220(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position67740625
GeneGNRHR
is asnp
is mentioned by
dbSNPrs515726220
ebirs515726220
HLIrs515726220
Exacrs515726220
Varsomers515726220
Maprs515726220
PheGenIrs515726220
hapmaprs515726220
1000 genomesrs515726220
hgdprs515726220
ensemblrs515726220
gopubmedrs515726220
geneviewrs515726220
scholarrs515726220
googlers515726220
pharmgkbrs515726220
gwascentralrs515726220
openSNPrs515726220
23andMers515726220
23andMe allrs515726220
SNP Nexus

SNPshotrs515726220
SNPdbers515726220
MSV3drs515726220
GWAS Ctlgrs515726220
Max Magnitude0
ClinVar
Risk rs515726220(A;A)
Alt rs515726220(A;A)
Reference rs515726220(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.68606343G>A
CLNSRC ClinVar Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000114424.1,