Have questions? Visit https://www.reddit.com/r/SNPedia

rs199865688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199865688(C;T)
Make rs199865688(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47337496
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs199865688
ebirs199865688
HLIrs199865688
Exacrs199865688
Varsomers199865688
Maprs199865688
PheGenIrs199865688
hapmaprs199865688
1000 genomesrs199865688
hgdprs199865688
ensemblrs199865688
gopubmedrs199865688
geneviewrs199865688
scholarrs199865688
googlers199865688
pharmgkbrs199865688
gwascentralrs199865688
openSNPrs199865688
23andMers199865688
23andMe allrs199865688
SNP Nexus

SNPshotrs199865688
SNPdbers199865688
MSV3drs199865688
GWAS Ctlgrs199865688
Max Magnitude0
ClinVar
Risk rs199865688(T;T)
Alt rs199865688(T;T)
Reference rs199865688(C;C)
Significance Other
Disease not specified Left ventricular noncompaction 10 Familial hypertrophic cardiomyopathy 4 Paroxysmal atrial fibrillation Primary familial hypertrophic cardiomyopathy Primary dilated cardiomyopathy Cardiomyopathy Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Left ventricular noncompaction 10 Familial hypertrophic cardiomyopathy 4 Paroxysmal atrial fibrillation Primary familial hypertrophic cardiomyopathy Primary dilated cardiomyopathy Cardiomyopathy Hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47359047C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000035494.5, RCV000054796.4, RCV000054797.5, RCV000143914.2, RCV000148656.2, RCV000157313.1, RCV000158162.1, RCV000234059.1,