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rs200625851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200625851(C;T)
Make rs200625851(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position47342734
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs200625851
ebirs200625851
HLIrs200625851
Exacrs200625851
Varsomers200625851
Maprs200625851
PheGenIrs200625851
hapmaprs200625851
1000 genomesrs200625851
hgdprs200625851
ensemblrs200625851
gopubmedrs200625851
geneviewrs200625851
scholarrs200625851
googlers200625851
pharmgkbrs200625851
gwascentralrs200625851
openSNPrs200625851
23andMers200625851
23andMe allrs200625851
SNP Nexus

SNPshotrs200625851
SNPdbers200625851
MSV3drs200625851
GWAS Ctlgrs200625851
Max Magnitude0
ClinVar
Risk rs200625851(T;T)
Alt rs200625851(T;T)
Reference rs200625851(C;C)
Significance Other
Disease not specified Familial hypertrophic cardiomyopathy 4 Left ventricular noncompaction 10 Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Familial hypertrophic cardiomyopathy 4 Left ventricular noncompaction 10 Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47364285C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000035402.4, RCV000054800.4, RCV000054834.4, RCV000148662.3, RCV000231699.1,