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rs397516003

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516003(A;A)
Make rs397516003(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333649
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516003
ebirs397516003
HLIrs397516003
Exacrs397516003
Varsomers397516003
Maprs397516003
PheGenIrs397516003
hapmaprs397516003
1000 genomesrs397516003
hgdprs397516003
ensemblrs397516003
gopubmedrs397516003
geneviewrs397516003
scholarrs397516003
googlers397516003
pharmgkbrs397516003
gwascentralrs397516003
openSNPrs397516003
23andMers397516003
23andMe allrs397516003
SNP Nexus

SNPshotrs397516003
SNPdbers397516003
MSV3drs397516003
GWAS Ctlgrs397516003
Max Magnitude0
ClinVar
Risk rs397516003(A;A)
Alt rs397516003(A;A)
Reference rs397516003(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYBPC3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000011.9:g.47355200C>T
CLNSRC
CLNACC RCV000035559.3, RCV000158456.1,