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rs534345197

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs534345197(C;T)
Make rs534345197(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47338630
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs534345197
ebirs534345197
HLIrs534345197
Exacrs534345197
Varsomers534345197
Maprs534345197
PheGenIrs534345197
hapmaprs534345197
1000 genomesrs534345197
hgdprs534345197
ensemblrs534345197
gopubmedrs534345197
geneviewrs534345197
scholarrs534345197
googlers534345197
pharmgkbrs534345197
gwascentralrs534345197
openSNPrs534345197
23andMers534345197
23andMe allrs534345197
SNP Nexus

SNPshotrs534345197
SNPdbers534345197
MSV3drs534345197
GWAS Ctlgrs534345197
Max Magnitude0
ClinVar
Risk rs534345197(A,T;A,T)
Alt rs534345197(A,T;A,T)
Reference rs534345197(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47360181C>T
CLNSRC
CLNACC RCV000158442.2,