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rs137853303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853303(C;T)
Make rs137853303(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position68522798
GenePRKAR1A
is asnp
is mentioned by
dbSNPrs137853303
ebirs137853303
HLIrs137853303
Exacrs137853303
Varsomers137853303
Maprs137853303
PheGenIrs137853303
hapmaprs137853303
1000 genomesrs137853303
hgdprs137853303
ensemblrs137853303
gopubmedrs137853303
geneviewrs137853303
scholarrs137853303
googlers137853303
pharmgkbrs137853303
gwascentralrs137853303
openSNPrs137853303
23andMers137853303
23andMe allrs137853303
SNP Nexus

SNPshotrs137853303
SNPdbers137853303
MSV3drs137853303
GWAS Ctlgrs137853303
Max Magnitude0
OMIM188830
Desc
Variant0013
Relatedalso
ClinVar
Risk rs137853303(T;T)
Alt rs137853303(T;T)
Reference rs137853303(C;C)
Significance Pathogenic
Disease Carney complex Carney complex
Variation info
Gene PRKAR1A
CLNDBN Carney complex, type 1 Carney complex
Reversed 0
HGVS NC_000017.10:g.66518939C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013510.17, RCV000148738.1,