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rs727505367

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727505367(G;G)
Make rs727505367(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position67753986
GeneGNRHR, LOC105377264
is asnp
is mentioned by
dbSNPrs727505367
ebirs727505367
HLIrs727505367
Exacrs727505367
Varsomers727505367
Maprs727505367
PheGenIrs727505367
hapmaprs727505367
1000 genomesrs727505367
hgdprs727505367
ensemblrs727505367
gopubmedrs727505367
geneviewrs727505367
scholarrs727505367
googlers727505367
pharmgkbrs727505367
gwascentralrs727505367
openSNPrs727505367
23andMers727505367
23andMe allrs727505367
SNP Nexus

SNPshotrs727505367
SNPdbers727505367
MSV3drs727505367
GWAS Ctlgrs727505367
Max Magnitude0
ClinVar
Risk rs727505367(G;G)
Alt rs727505367(G;G)
Reference rs727505367(T;T)
Significance Probable-Pathogenic
Disease Delayed puberty
Variation info
Gene GNRHR
CLNDBN Delayed puberty
Reversed 1
HGVS NC_000004.11:g.68619704A>C
CLNSRC
CLNACC RCV000156945.1,