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rs397516406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516406(A;A)
Make rs397516406(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position110911093
GeneMYL2
is asnp
is mentioned by
dbSNPrs397516406
ebirs397516406
HLIrs397516406
Exacrs397516406
Varsomers397516406
Maprs397516406
PheGenIrs397516406
hapmaprs397516406
1000 genomesrs397516406
hgdprs397516406
ensemblrs397516406
gopubmedrs397516406
geneviewrs397516406
scholarrs397516406
googlers397516406
pharmgkbrs397516406
gwascentralrs397516406
openSNPrs397516406
23andMers397516406
23andMe allrs397516406
SNP Nexus

SNPshotrs397516406
SNPdbers397516406
MSV3drs397516406
GWAS Ctlgrs397516406
Max Magnitude0
ClinVar
Risk rs397516406(A;A)
Alt rs397516406(A;A)
Reference rs397516406(G;G)
Significance Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene MYL2
CLNDBN not specified Cardiomyopathy
Reversed 1
HGVS NC_000012.11:g.111348897C>T
CLNSRC ClinVar
CLNACC RCV000036408.3, RCV000158906.1,