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rs199669878

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199669878(C;T)
Make rs199669878(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332658
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs199669878
ebirs199669878
HLIrs199669878
Exacrs199669878
Varsomers199669878
Maprs199669878
PheGenIrs199669878
hapmaprs199669878
1000 genomesrs199669878
hgdprs199669878
ensemblrs199669878
gopubmedrs199669878
geneviewrs199669878
scholarrs199669878
googlers199669878
pharmgkbrs199669878
gwascentralrs199669878
openSNPrs199669878
23andMers199669878
23andMe allrs199669878
SNP Nexus

SNPshotrs199669878
SNPdbers199669878
MSV3drs199669878
GWAS Ctlgrs199669878
Max Magnitude0
ClinVar
Risk rs199669878(T;T)
Alt rs199669878(T;T)
Reference rs199669878(C;C)
Significance Probable-non-pathogenic
Disease not specified not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified not provided Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47354209C>T
CLNSRC
CLNACC RCV000035594.5, RCV000172003.1, RCV000234600.1,