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rs730880635

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880635(C;T)
Make rs730880635(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343595
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880635
ebirs730880635
HLIrs730880635
Exacrs730880635
Varsomers730880635
Maprs730880635
PheGenIrs730880635
hapmaprs730880635
1000 genomesrs730880635
hgdprs730880635
ensemblrs730880635
gopubmedrs730880635
geneviewrs730880635
scholarrs730880635
googlers730880635
pharmgkbrs730880635
gwascentralrs730880635
openSNPrs730880635
23andMers730880635
23andMe allrs730880635
SNP Nexus

SNPshotrs730880635
SNPdbers730880635
MSV3drs730880635
GWAS Ctlgrs730880635
Max Magnitude0
ClinVar
Risk rs730880635(A,T;A,T)
Alt rs730880635(A,T;A,T)
Reference rs730880635(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47365146G>A
CLNSRC
CLNACC RCV000158333.1,