Have questions? Visit https://www.reddit.com/r/SNPedia

rs281864797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281864797(C;C)
Make rs281864797(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position68522927
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864797
ebirs281864797
HLIrs281864797
Exacrs281864797
Varsomers281864797
Maprs281864797
PheGenIrs281864797
hapmaprs281864797
1000 genomesrs281864797
hgdprs281864797
ensemblrs281864797
gopubmedrs281864797
geneviewrs281864797
scholarrs281864797
googlers281864797
pharmgkbrs281864797
gwascentralrs281864797
openSNPrs281864797
23andMers281864797
23andMe allrs281864797
SNP Nexus

SNPshotrs281864797
SNPdbers281864797
MSV3drs281864797
GWAS Ctlgrs281864797
Max Magnitude0
ClinVar
Risk rs281864797(C;C)
Alt rs281864797(C;C)
Reference rs281864797(G;G)
Significance Pathogenic
Disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1
Reversed 0
HGVS NC_000017.10:g.66519068G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034289.2,