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rs587776978

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776978(A;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position89351811
GeneDUSP6
is asnp
is mentioned by
dbSNPrs587776978
ebirs587776978
HLIrs587776978
Exacrs587776978
Varsomers587776978
Maprs587776978
PheGenIrs587776978
hapmaprs587776978
1000 genomesrs587776978
hgdprs587776978
ensemblrs587776978
gopubmedrs587776978
geneviewrs587776978
scholarrs587776978
googlers587776978
pharmgkbrs587776978
gwascentralrs587776978
openSNPrs587776978
23andMers587776978
23andMe allrs587776978
SNP Nexus

SNPshotrs587776978
SNPdbers587776978
MSV3drs587776978
GWAS Ctlgrs587776978
Max Magnitude0
ClinVar
Risk rs587776978(A;A)
Alt rs587776978(A;A)
Reference rs587776978(T;T)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 19 with or without anosmia
Variation info
Gene DUSP6
CLNDBN Hypogonadotropic hypogonadism 19 with or without anosmia
Reversed 1
HGVS NC_000012.11:g.89745588A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043597.2,