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rs587777022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777022(C;G)
Make rs587777022(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position3118950
GeneGNA11
is asnp
is mentioned by
dbSNPrs587777022
ebirs587777022
HLIrs587777022
Exacrs587777022
Varsomers587777022
Maprs587777022
PheGenIrs587777022
hapmaprs587777022
1000 genomesrs587777022
hgdprs587777022
ensemblrs587777022
gopubmedrs587777022
geneviewrs587777022
scholarrs587777022
googlers587777022
pharmgkbrs587777022
gwascentralrs587777022
openSNPrs587777022
23andMers587777022
23andMe allrs587777022
SNP Nexus

SNPshotrs587777022
SNPdbers587777022
MSV3drs587777022
GWAS Ctlgrs587777022
Max Magnitude0
ClinVar
Risk rs587777022(G,T;G,T)
Alt rs587777022(G,T;G,T)
Reference rs587777022(C;C)
Significance Pathogenic
Disease Hypocalcemia
Variation info
Gene GNA11
CLNDBN Hypocalcemia, autosomal dominant 2
Reversed 0
HGVS NC_000019.9:g.3118948C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000054479.27,