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rs281864782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864782(C;T)
Make rs281864782(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position68515523
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864782
ClinGenrs281864782
ebirs281864782
HLIrs281864782
Exacrs281864782
Varsomers281864782
Maprs281864782
PheGenIrs281864782
hapmaprs281864782
1000 genomesrs281864782
hgdprs281864782
ensemblrs281864782
gopubmedrs281864782
geneviewrs281864782
scholarrs281864782
googlers281864782
pharmgkbrs281864782
gwascentralrs281864782
openSNPrs281864782
23andMers281864782
23andMe allrs281864782
SNP Nexus

SNPshotrs281864782
SNPdbers281864782
MSV3drs281864782
GWAS Ctlgrs281864782
Max Magnitude0
ClinVar
Risk rs281864782(G;G) rs281864782(T;T)
Alt rs281864782(G;G) rs281864782(T;T)
Reference Rs281864782(C;C)
Significance Pathogenic
Disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1
Reversed 0
HGVS NC_000017.10:g.66511664C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034284.2,