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rs200411226

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200411226(C;T)
Make rs200411226(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342718
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs200411226
ebirs200411226
HLIrs200411226
Exacrs200411226
Varsomers200411226
Maprs200411226
PheGenIrs200411226
hapmaprs200411226
1000 genomesrs200411226
hgdprs200411226
ensemblrs200411226
gopubmedrs200411226
geneviewrs200411226
scholarrs200411226
googlers200411226
pharmgkbrs200411226
gwascentralrs200411226
openSNPrs200411226
23andMers200411226
23andMe allrs200411226
SNP Nexus

SNPshotrs200411226
SNPdbers200411226
MSV3drs200411226
GWAS Ctlgrs200411226
Max Magnitude0
ClinVar
Risk rs200411226(T;T)
Alt rs200411226(T;T)
Reference rs200411226(C;C)
Significance Other
Disease Hypertrophic cardiomyopathy Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided
Variation info
Gene MYBPC3
CLNDBN Hypertrophic cardiomyopathy Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided
Reversed 0
HGVS NC_000011.9:g.47364269C>T
CLNSRC
CLNACC RCV000168090.3, RCV000171824.3, RCV000201509.1, RCV000223693.1,