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rs371401403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371401403(G;T)
Make rs371401403(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47335996
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs371401403
ebirs371401403
HLIrs371401403
Exacrs371401403
Varsomers371401403
Maprs371401403
PheGenIrs371401403
hapmaprs371401403
1000 genomesrs371401403
hgdprs371401403
ensemblrs371401403
gopubmedrs371401403
geneviewrs371401403
scholarrs371401403
googlers371401403
pharmgkbrs371401403
gwascentralrs371401403
openSNPrs371401403
23andMers371401403
23andMe allrs371401403
SNP Nexus

SNPshotrs371401403
SNPdbers371401403
MSV3drs371401403
GWAS Ctlgrs371401403
Max Magnitude0
ClinVar
Risk rs371401403(A,T;A,T)
Alt rs371401403(A,T;A,T)
Reference rs371401403(G;G)
Significance Pathogenic
Disease Left ventricular noncompaction 10 not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYBPC3
CLNDBN Left ventricular noncompaction 10 not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 not provided Familial hypertrophic cardiomyopathy 1
Reversed 0
HGVS NC_000011.9:g.47357547G>A; NC_000011.9:g.47357547G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054802.3, RCV000158446.2, RCV000171835.1, RCV000023054.4, RCV000035516.5, RCV000148675.1, RCV000158177.2, RCV000201917.1,