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rs587777707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777707(G;T)
Make rs587777707(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position3110191
GeneGNA11
is asnp
is mentioned by
dbSNPrs587777707
ebirs587777707
HLIrs587777707
Exacrs587777707
Varsomers587777707
Maprs587777707
PheGenIrs587777707
hapmaprs587777707
1000 genomesrs587777707
hgdprs587777707
ensemblrs587777707
gopubmedrs587777707
geneviewrs587777707
scholarrs587777707
googlers587777707
pharmgkbrs587777707
gwascentralrs587777707
openSNPrs587777707
23andMers587777707
23andMe allrs587777707
SNP Nexus

SNPshotrs587777707
SNPdbers587777707
MSV3drs587777707
GWAS Ctlgrs587777707
Max Magnitude0
ClinVar
Risk rs587777707(T;T)
Alt rs587777707(T;T)
Reference rs587777707(G;G)
Significance Pathogenic
Disease Hypocalcemia
Variation info
Gene GNA11
CLNDBN Hypocalcemia, autosomal dominant 2
Reversed 0
HGVS NC_000019.9:g.3110189G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144048.2,