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

rs727504722

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504722(A;A)
Make rs727504722(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332122
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs727504722
ebirs727504722
HLIrs727504722
Exacrs727504722
Varsomers727504722
Maprs727504722
PheGenIrs727504722
hapmaprs727504722
1000 genomesrs727504722
hgdprs727504722
ensemblrs727504722
gopubmedrs727504722
geneviewrs727504722
scholarrs727504722
googlers727504722
pharmgkbrs727504722
gwascentralrs727504722
openSNPrs727504722
23andMers727504722
23andMe allrs727504722
SNP Nexus

SNPshotrs727504722
SNPdbers727504722
MSV3drs727504722
GWAS Ctlgrs727504722
Max Magnitude0
ClinVar
Risk rs727504722(A;A)
Alt rs727504722(A;A)
Reference rs727504722(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47353673G>T
CLNSRC
CLNACC RCV000156014.1,