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rs587776773

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776773(A;A)
Make rs587776773(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position68512549
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs587776773
ebirs587776773
HLIrs587776773
Exacrs587776773
Varsomers587776773
Maprs587776773
PheGenIrs587776773
hapmaprs587776773
1000 genomesrs587776773
hgdprs587776773
ensemblrs587776773
gopubmedrs587776773
geneviewrs587776773
scholarrs587776773
googlers587776773
pharmgkbrs587776773
gwascentralrs587776773
openSNPrs587776773
23andMers587776773
23andMe allrs587776773
SNP Nexus

SNPshotrs587776773
SNPdbers587776773
MSV3drs587776773
GWAS Ctlgrs587776773
Max Magnitude0
ClinVar
Risk rs587776773(A;A)
Alt rs587776773(A;A)
Reference rs587776773(G;G)
Significance Pathogenic
Disease Pigmented nodular adrenocortical disease
Variation info
Gene PRKAR1A
CLNDBN Pigmented nodular adrenocortical disease, primary, 1
Reversed 0
HGVS NC_000017.10:g.66508690G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013506.25,