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rs281864799

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281864799(A;G)
Make rs281864799(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position68528994
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864799
ebirs281864799
HLIrs281864799
Exacrs281864799
Varsomers281864799
Maprs281864799
PheGenIrs281864799
hapmaprs281864799
1000 genomesrs281864799
hgdprs281864799
ensemblrs281864799
gopubmedrs281864799
geneviewrs281864799
scholarrs281864799
googlers281864799
pharmgkbrs281864799
gwascentralrs281864799
openSNPrs281864799
23andMers281864799
23andMe allrs281864799
SNP Nexus

SNPshotrs281864799
SNPdbers281864799
MSV3drs281864799
GWAS Ctlgrs281864799
Max Magnitude0
ClinVar
Risk rs281864799(G;G)
Alt rs281864799(G;G)
Reference rs281864799(A;A)
Significance Pathogenic
Disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1
Reversed 0
HGVS NC_000017.10:g.66525135A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013500.24,