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rs724160013

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs724160013(-;-)
Make rs724160013(-;GTG)
Make rs724160013(GTG;GTG)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position14097621
GenePRKACA
is asnp
is mentioned by
dbSNPrs724160013
ebirs724160013
HLIrs724160013
Exacrs724160013
Varsomers724160013
Maprs724160013
PheGenIrs724160013
hapmaprs724160013
1000 genomesrs724160013
hgdprs724160013
ensemblrs724160013
gopubmedrs724160013
geneviewrs724160013
scholarrs724160013
googlers724160013
pharmgkbrs724160013
gwascentralrs724160013
openSNPrs724160013
23andMers724160013
23andMe allrs724160013
SNP Nexus

SNPshotrs724160013
SNPdbers724160013
MSV3drs724160013
GWAS Ctlgrs724160013
Max Magnitude0
ClinVar
Risk rs724160013(GTG;GTG)
Alt rs724160013(GTG;GTG)
Reference rs724160013(;)
Significance Pathogenic
Disease Pigmented nodular adrenocortical disease
Variation info
Gene PRKACA
CLNDBN Pigmented nodular adrenocortical disease, primary, 4
Reversed 1
HGVS NC_000019.9:g.14208434_14208436dupCAC
CLNSRC
CLNACC RCV000149856.1,