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rs587776774

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776774(A;A)
Make rs587776774(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position68529919
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs587776774
ebirs587776774
HLIrs587776774
Exacrs587776774
Varsomers587776774
Maprs587776774
PheGenIrs587776774
hapmaprs587776774
1000 genomesrs587776774
hgdprs587776774
ensemblrs587776774
gopubmedrs587776774
geneviewrs587776774
scholarrs587776774
googlers587776774
pharmgkbrs587776774
gwascentralrs587776774
openSNPrs587776774
23andMers587776774
23andMe allrs587776774
SNP Nexus

SNPshotrs587776774
SNPdbers587776774
MSV3drs587776774
GWAS Ctlgrs587776774
Max Magnitude0
ClinVar
Risk rs587776774(A;A)
Alt rs587776774(A;A)
Reference rs587776774(G;G)
Significance Pathogenic
Disease Adrenocortical tumor
Variation info
Gene PRKAR1A
CLNDBN Adrenocortical tumor, somatic
Reversed 0
HGVS NC_000017.10:g.66526060G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013509.5,