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rs587776981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776981(C;T)
Make rs587776981(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position142315063
GeneSPRY4
is asnp
is mentioned by
dbSNPrs587776981
ebirs587776981
HLIrs587776981
Exacrs587776981
Varsomers587776981
Maprs587776981
PheGenIrs587776981
hapmaprs587776981
1000 genomesrs587776981
hgdprs587776981
ensemblrs587776981
gopubmedrs587776981
geneviewrs587776981
scholarrs587776981
googlers587776981
pharmgkbrs587776981
gwascentralrs587776981
openSNPrs587776981
23andMers587776981
23andMe allrs587776981
SNP Nexus

SNPshotrs587776981
SNPdbers587776981
MSV3drs587776981
GWAS Ctlgrs587776981
Max Magnitude0
ClinVar
Risk rs587776981(C,T;C,T)
Alt rs587776981(C,T;C,T)
Reference rs587776981(G;G)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 17 with or without anosmia
Variation info
Gene SPRY4
CLNDBN Hypogonadotropic hypogonadism 17 with or without anosmia
Reversed 1
HGVS NC_000005.9:g.141694628C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043617.2,