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rs587777021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777021(C;T)
Make rs587777021(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position3110190
GeneGNA11
is asnp
is mentioned by
dbSNPrs587777021
ebirs587777021
HLIrs587777021
Exacrs587777021
Varsomers587777021
Maprs587777021
PheGenIrs587777021
hapmaprs587777021
1000 genomesrs587777021
hgdprs587777021
ensemblrs587777021
gopubmedrs587777021
geneviewrs587777021
scholarrs587777021
googlers587777021
pharmgkbrs587777021
gwascentralrs587777021
openSNPrs587777021
23andMers587777021
23andMe allrs587777021
SNP Nexus

SNPshotrs587777021
SNPdbers587777021
MSV3drs587777021
GWAS Ctlgrs587777021
Max Magnitude0
ClinVar
Risk rs587777021(T;T)
Alt rs587777021(T;T)
Reference rs587777021(C;C)
Significance Pathogenic
Disease Hypocalcemia
Variation info
Gene GNA11
CLNDBN Hypocalcemia, autosomal dominant 2
Reversed 0
HGVS NC_000019.9:g.3110188C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054478.27,