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rs587777019

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777019(A;A)
Make rs587777019(A;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position3113412
GeneGNA11
is asnp
is mentioned by
dbSNPrs587777019
ebirs587777019
HLIrs587777019
Exacrs587777019
Varsomers587777019
Maprs587777019
PheGenIrs587777019
hapmaprs587777019
1000 genomesrs587777019
hgdprs587777019
ensemblrs587777019
gopubmedrs587777019
geneviewrs587777019
scholarrs587777019
googlers587777019
pharmgkbrs587777019
gwascentralrs587777019
openSNPrs587777019
23andMers587777019
23andMe allrs587777019
SNP Nexus

SNPshotrs587777019
SNPdbers587777019
MSV3drs587777019
GWAS Ctlgrs587777019
Max Magnitude0
ClinVar
Risk rs587777019(A;A)
Alt rs587777019(A;A)
Reference rs587777019(T;T)
Significance Pathogenic
Disease Hypocalciuric hypercalcemia
Variation info
Gene GNA11
CLNDBN Hypocalciuric hypercalcemia, familial, type II
Reversed 0
HGVS NC_000019.9:g.3113410T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054475.26,