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rs724159972

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724159972(C;G)
Make rs724159972(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position69013871
GenePRKACG
is asnp
is mentioned by
dbSNPrs724159972
ebirs724159972
HLIrs724159972
Exacrs724159972
Varsomers724159972
Maprs724159972
PheGenIrs724159972
hapmaprs724159972
1000 genomesrs724159972
hgdprs724159972
ensemblrs724159972
gopubmedrs724159972
geneviewrs724159972
scholarrs724159972
googlers724159972
pharmgkbrs724159972
gwascentralrs724159972
openSNPrs724159972
23andMers724159972
23andMe allrs724159972
SNP Nexus

SNPshotrs724159972
SNPdbers724159972
MSV3drs724159972
GWAS Ctlgrs724159972
Max Magnitude0
ClinVar
Risk rs724159972(G;G)
Alt rs724159972(G;G)
Reference rs724159972(C;C)
Significance Pathogenic
Disease Platelet-type bleeding disorder 19
Variation info
Gene PRKACG
CLNDBN Platelet-type bleeding disorder 19
Reversed 1
HGVS NC_000009.11:g.71628787G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000149789.3,