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

rs727504887

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504887(G;T)
Make rs727504887(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47342127
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504887
ebirs727504887
HLIrs727504887
Exacrs727504887
Varsomers727504887
Maprs727504887
PheGenIrs727504887
hapmaprs727504887
1000 genomesrs727504887
hgdprs727504887
ensemblrs727504887
gopubmedrs727504887
geneviewrs727504887
scholarrs727504887
googlers727504887
pharmgkbrs727504887
gwascentralrs727504887
openSNPrs727504887
23andMers727504887
23andMe allrs727504887
SNP Nexus

SNPshotrs727504887
SNPdbers727504887
MSV3drs727504887
GWAS Ctlgrs727504887
Max Magnitude0
ClinVar
Risk rs727504887(T;T)
Alt rs727504887(T;T)
Reference rs727504887(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000011.9:g.47363678C>A
CLNSRC
CLNACC RCV000156263.1, RCV000158433.2,