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rs727504235

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504235(A;A)
Make rs727504235(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47333742
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504235
ebirs727504235
HLIrs727504235
Exacrs727504235
Varsomers727504235
Maprs727504235
PheGenIrs727504235
hapmaprs727504235
1000 genomesrs727504235
hgdprs727504235
ensemblrs727504235
gopubmedrs727504235
geneviewrs727504235
scholarrs727504235
googlers727504235
pharmgkbrs727504235
gwascentralrs727504235
openSNPrs727504235
23andMers727504235
23andMe allrs727504235
SNP Nexus

SNPshotrs727504235
SNPdbers727504235
MSV3drs727504235
GWAS Ctlgrs727504235
Max Magnitude0
ClinVar
Risk rs727504235(A;A)
Alt rs727504235(A;A)
Reference rs727504235(G;G)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355293C>T
CLNSRC
CLNACC RCV000154201.2, RCV000208257.1,