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rs587777758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777758(-;-)
Make rs587777758(-;T)
Make rs587777758(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position25423313
GeneGNRH1
is asnp
is mentioned by
dbSNPrs587777758
ebirs587777758
HLIrs587777758
Exacrs587777758
Varsomers587777758
Maprs587777758
PheGenIrs587777758
hapmaprs587777758
1000 genomesrs587777758
hgdprs587777758
ensemblrs587777758
gopubmedrs587777758
geneviewrs587777758
scholarrs587777758
googlers587777758
pharmgkbrs587777758
gwascentralrs587777758
openSNPrs587777758
23andMers587777758
23andMe allrs587777758
SNP Nexus

SNPshotrs587777758
SNPdbers587777758
MSV3drs587777758
GWAS Ctlgrs587777758
Max Magnitude0
ClinVar
Risk rs587777758(T;T)
Alt rs587777758(T;T)
Reference rs587777758(;)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 12 with or without anosmia
Variation info
Gene GNRH1
CLNDBN Hypogonadotropic hypogonadism 12 with or without anosmia
Reversed 0
HGVS NC_000008.10:g.25280829dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000030900.29,