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rs281864785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs281864785(CT;CT)
Make rs281864785(CT;GG)
ReferenceGRCh38 38.1/141
Chromosome17
Position68528886
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864785
ebirs281864785
HLIrs281864785
Exacrs281864785
Varsomers281864785
Maprs281864785
PheGenIrs281864785
hapmaprs281864785
1000 genomesrs281864785
hgdprs281864785
ensemblrs281864785
gopubmedrs281864785
geneviewrs281864785
scholarrs281864785
googlers281864785
pharmgkbrs281864785
gwascentralrs281864785
openSNPrs281864785
23andMers281864785
23andMe allrs281864785
SNP Nexus

SNPshotrs281864785
SNPdbers281864785
MSV3drs281864785
GWAS Ctlgrs281864785
Max Magnitude0
ClinVar
Risk rs281864785(CT;CT)
Alt rs281864785(CT;CT)
Reference rs281864785(GG;GG)
Significance Pathogenic
Disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1
Reversed 0
HGVS NC_000017.10:g.66525027_66525028delGGinsCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000013499.25,