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rs587777020

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777020(A;A)
Make rs587777020(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position3115009
GeneGNA11
is asnp
is mentioned by
dbSNPrs587777020
ebirs587777020
HLIrs587777020
Exacrs587777020
Varsomers587777020
Maprs587777020
PheGenIrs587777020
hapmaprs587777020
1000 genomesrs587777020
hgdprs587777020
ensemblrs587777020
gopubmedrs587777020
geneviewrs587777020
scholarrs587777020
googlers587777020
pharmgkbrs587777020
gwascentralrs587777020
openSNPrs587777020
23andMers587777020
23andMe allrs587777020
SNP Nexus

SNPshotrs587777020
SNPdbers587777020
MSV3drs587777020
GWAS Ctlgrs587777020
Max Magnitude0
ClinVar
Risk rs587777020(A;A)
Alt rs587777020(A;A)
Reference rs587777020(G;G)
Significance Pathogenic
Disease Hypocalcemia
Variation info
Gene GNA11
CLNDBN Hypocalcemia, autosomal dominant 2
Reversed 0
HGVS NC_000019.9:g.3115007G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054476.27,