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

rs281864784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281864784(C;T)
Make rs281864784(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position68525886
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864784
dbSNP (classic)rs281864784
ClinGenrs281864784
ebirs281864784
HLIrs281864784
Exacrs281864784
Gnomadrs281864784
Varsomers281864784
LitVarrs281864784
Maprs281864784
PheGenIrs281864784
Biobankrs281864784
1000 genomesrs281864784
hgdprs281864784
ensemblrs281864784
geneviewrs281864784
scholarrs281864784
googlers281864784
pharmgkbrs281864784
gwascentralrs281864784
openSNPrs281864784
23andMers281864784
SNPshotrs281864784
SNPdbers281864784
MSV3drs281864784
GWAS Ctlgrs281864784
Max Magnitude0
ClinVar
Risk rs281864784(T;T)
Alt rs281864784(T;T)
Reference Rs281864784(C;C)
Significance Pathogenic
Disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1
Reversed 0
HGVS NC_000017.10:g.66522027C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034293.2,