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rs397516135

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516135(A;A)
Make rs397516135(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23425813
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516135
ebirs397516135
HLIrs397516135
Exacrs397516135
Varsomers397516135
Maprs397516135
PheGenIrs397516135
hapmaprs397516135
1000 genomesrs397516135
hgdprs397516135
ensemblrs397516135
gopubmedrs397516135
geneviewrs397516135
scholarrs397516135
googlers397516135
pharmgkbrs397516135
gwascentralrs397516135
openSNPrs397516135
23andMers397516135
23andMe allrs397516135
SNP Nexus

SNPshotrs397516135
SNPdbers397516135
MSV3drs397516135
GWAS Ctlgrs397516135
Max Magnitude0
ClinVar
Risk rs397516135(A;A)
Alt rs397516135(A;A)
Reference rs397516135(G;G)
Significance Pathogenic
Disease not specified Familial cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Familial cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23895022C>T
CLNSRC ClinVar
CLNACC RCV000035773.3, RCV000148962.1,