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rs730880601

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880601(C;C)
Make rs730880601(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332135
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880601
ebirs730880601
HLIrs730880601
Exacrs730880601
Varsomers730880601
Maprs730880601
PheGenIrs730880601
hapmaprs730880601
1000 genomesrs730880601
hgdprs730880601
ensemblrs730880601
gopubmedrs730880601
geneviewrs730880601
scholarrs730880601
googlers730880601
pharmgkbrs730880601
gwascentralrs730880601
openSNPrs730880601
23andMers730880601
23andMe allrs730880601
SNP Nexus

SNPshotrs730880601
SNPdbers730880601
MSV3drs730880601
GWAS Ctlgrs730880601
Max Magnitude0
ClinVar
Risk rs730880601(C;C)
Alt rs730880601(C;C)
Reference rs730880601(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47353686A>G
CLNSRC
CLNACC RCV000223863.2,