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

rs727505152

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727505152(-;-)
Make rs727505152(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343042
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727505152
ebirs727505152
HLIrs727505152
Exacrs727505152
Varsomers727505152
Maprs727505152
PheGenIrs727505152
hapmaprs727505152
1000 genomesrs727505152
hgdprs727505152
ensemblrs727505152
gopubmedrs727505152
geneviewrs727505152
scholarrs727505152
googlers727505152
pharmgkbrs727505152
gwascentralrs727505152
openSNPrs727505152
23andMers727505152
23andMe allrs727505152
SNP Nexus

SNPshotrs727505152
SNPdbers727505152
MSV3drs727505152
GWAS Ctlgrs727505152
Max Magnitude0
ClinVar
Risk rs727505152(;)
Alt rs727505152(;)
Reference rs727505152(A;A)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364593delT
CLNSRC
CLNACC RCV000156620.1,