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rs727504371

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs727504371(A;A)
Make rs727504371(A;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47336009
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504371
ebirs727504371
HLIrs727504371
Exacrs727504371
Varsomers727504371
Maprs727504371
PheGenIrs727504371
hapmaprs727504371
1000 genomesrs727504371
hgdprs727504371
ensemblrs727504371
gopubmedrs727504371
geneviewrs727504371
scholarrs727504371
googlers727504371
pharmgkbrs727504371
gwascentralrs727504371
openSNPrs727504371
23andMers727504371
23andMe allrs727504371
SNP Nexus

SNPshotrs727504371
SNPdbers727504371
MSV3drs727504371
GWAS Ctlgrs727504371
Max Magnitude0
ClinVar
Risk rs727504371(A;A)
Alt rs727504371(A;A)
Reference rs727504371(TC;TC)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47357560_47357561delinsT
CLNSRC
CLNACC RCV000154510.2,