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rs730880696

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880696(A;A)
Make rs730880696(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47338664
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880696
ebirs730880696
HLIrs730880696
Exacrs730880696
Varsomers730880696
Maprs730880696
PheGenIrs730880696
hapmaprs730880696
1000 genomesrs730880696
hgdprs730880696
ensemblrs730880696
gopubmedrs730880696
geneviewrs730880696
scholarrs730880696
googlers730880696
pharmgkbrs730880696
gwascentralrs730880696
openSNPrs730880696
23andMers730880696
23andMe allrs730880696
SNP Nexus

SNPshotrs730880696
SNPdbers730880696
MSV3drs730880696
GWAS Ctlgrs730880696
Max Magnitude0
ClinVar
Risk rs730880696(A;A) rs730880696(C;C)
Alt rs730880696(A;A) rs730880696(C;C)
Reference Rs730880696(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47360215C>T
CLNSRC
CLNACC RCV000158441.2,