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rs281864798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281864798(G;T)
Make rs281864798(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position68525913
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs281864798
dbSNP (classic)rs281864798
ClinGenrs281864798
ebirs281864798
HLIrs281864798
Exacrs281864798
Gnomadrs281864798
Varsomers281864798
LitVarrs281864798
Maprs281864798
PheGenIrs281864798
Biobankrs281864798
1000 genomesrs281864798
hgdprs281864798
ensemblrs281864798
geneviewrs281864798
scholarrs281864798
googlers281864798
pharmgkbrs281864798
gwascentralrs281864798
openSNPrs281864798
23andMers281864798
SNPshotrs281864798
SNPdbers281864798
MSV3drs281864798
GWAS Ctlgrs281864798
Max Magnitude0
ClinVar
Risk rs281864798(T;T)
Alt rs281864798(T;T)
Reference Rs281864798(G;G)
Significance Pathogenic
Disease Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1
Reversed 0
HGVS NC_000017.10:g.66522054G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013508.19,