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rs386352352

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs386352352(G;G)
Make rs386352352(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position14097604
GenePRKACA
is asnp
is mentioned by
dbSNPrs386352352
ebirs386352352
HLIrs386352352
Exacrs386352352
Varsomers386352352
Maprs386352352
PheGenIrs386352352
hapmaprs386352352
1000 genomesrs386352352
hgdprs386352352
ensemblrs386352352
gopubmedrs386352352
geneviewrs386352352
scholarrs386352352
googlers386352352
pharmgkbrs386352352
gwascentralrs386352352
openSNPrs386352352
23andMers386352352
23andMe allrs386352352
SNP Nexus

SNPshotrs386352352
SNPdbers386352352
MSV3drs386352352
GWAS Ctlgrs386352352
Max Magnitude0
ClinVar
Risk rs386352352(G;G)
Alt rs386352352(G;G)
Reference rs386352352(T;T)
Significance Pathogenic
Disease Pigmented nodular adrenocortical disease not provided
Variation info
Gene PRKACA
CLNDBN Pigmented nodular adrenocortical disease, primary, 4 not provided
Reversed 1
HGVS NC_000019.9:g.14208416A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000119834.5, RCV000122662.1,