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rs730880695

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880695(C;C)
Make rs730880695(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342085
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880695
ebirs730880695
HLIrs730880695
Exacrs730880695
Varsomers730880695
Maprs730880695
PheGenIrs730880695
hapmaprs730880695
1000 genomesrs730880695
hgdprs730880695
ensemblrs730880695
gopubmedrs730880695
geneviewrs730880695
scholarrs730880695
googlers730880695
pharmgkbrs730880695
gwascentralrs730880695
openSNPrs730880695
23andMers730880695
23andMe allrs730880695
SNP Nexus

SNPshotrs730880695
SNPdbers730880695
MSV3drs730880695
GWAS Ctlgrs730880695
Max Magnitude0
ClinVar
Risk rs730880695(C;C)
Alt rs730880695(C;C)
Reference rs730880695(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47363636A>G
CLNSRC
CLNACC RCV000158437.2,