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rs727504287

From SNPedia

Orientationminus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs727504287(-;-)
Make rs727504287(-;AAG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342687
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504287
ebirs727504287
HLIrs727504287
Exacrs727504287
Varsomers727504287
Maprs727504287
PheGenIrs727504287
hapmaprs727504287
1000 genomesrs727504287
hgdprs727504287
ensemblrs727504287
gopubmedrs727504287
geneviewrs727504287
scholarrs727504287
googlers727504287
pharmgkbrs727504287
gwascentralrs727504287
openSNPrs727504287
23andMers727504287
23andMe allrs727504287
SNP Nexus

SNPshotrs727504287
SNPdbers727504287
MSV3drs727504287
GWAS Ctlgrs727504287
Max Magnitude0
ClinVar
Risk rs727504287(;)
Alt rs727504287(;)
Reference rs727504287(AAG;AAG)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 4
Variation info
Gene MYBPC3
CLNDBN not specified Familial hypertrophic cardiomyopathy 4
Reversed 1
HGVS NC_000011.9:g.47364238_47364240delCTT
CLNSRC
CLNACC RCV000154300.2, RCV000201476.1,