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rs730880624

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880624(C;C)
Make rs730880624(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47348487
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880624
ebirs730880624
HLIrs730880624
Exacrs730880624
Varsomers730880624
Maprs730880624
PheGenIrs730880624
hapmaprs730880624
1000 genomesrs730880624
hgdprs730880624
ensemblrs730880624
gopubmedrs730880624
geneviewrs730880624
scholarrs730880624
googlers730880624
pharmgkbrs730880624
gwascentralrs730880624
openSNPrs730880624
23andMers730880624
23andMe allrs730880624
SNP Nexus

SNPshotrs730880624
SNPdbers730880624
MSV3drs730880624
GWAS Ctlgrs730880624
Max Magnitude0
ClinVar
Risk rs730880624(C;C)
Alt rs730880624(C;C)
Reference rs730880624(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47370038A>G
CLNSRC
CLNACC RCV000158306.2,