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rs606231406

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs606231406(C;C)
Make rs606231406(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position67753944
GeneGNRHR, LOC105377264
is asnp
is mentioned by
dbSNPrs606231406
ebirs606231406
HLIrs606231406
Exacrs606231406
Varsomers606231406
Maprs606231406
PheGenIrs606231406
hapmaprs606231406
1000 genomesrs606231406
hgdprs606231406
ensemblrs606231406
gopubmedrs606231406
geneviewrs606231406
scholarrs606231406
googlers606231406
pharmgkbrs606231406
gwascentralrs606231406
openSNPrs606231406
23andMers606231406
23andMe allrs606231406
SNP Nexus

SNPshotrs606231406
SNPdbers606231406
MSV3drs606231406
GWAS Ctlgrs606231406
Max Magnitude0
ClinVar
Risk rs606231406(C;C)
Alt rs606231406(C;C)
Reference rs606231406(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 1
HGVS NC_000004.11:g.68619662A>G
CLNSRC
CLNACC RCV000128826.1,