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rs111437311

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111437311(A;T)
Make rs111437311(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342576
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs111437311
ebirs111437311
HLIrs111437311
Exacrs111437311
Varsomers111437311
Maprs111437311
PheGenIrs111437311
hapmaprs111437311
1000 genomesrs111437311
hgdprs111437311
ensemblrs111437311
gopubmedrs111437311
geneviewrs111437311
scholarrs111437311
googlers111437311
pharmgkbrs111437311
gwascentralrs111437311
openSNPrs111437311
23andMers111437311
23andMe allrs111437311
SNP Nexus

SNPshotrs111437311
SNPdbers111437311
MSV3drs111437311
GWAS Ctlgrs111437311
Max Magnitude0
ClinVar
Risk rs111437311(G,T;G,T)
Alt rs111437311(G,T;G,T)
Reference rs111437311(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 0
HGVS NC_000011.9:g.47364127A>G
CLNSRC
CLNACC RCV000151121.2, RCV000158105.1,