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rs397516165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516165(A;A)
Make rs397516165(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424118
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516165
ebirs397516165
HLIrs397516165
Exacrs397516165
Varsomers397516165
Maprs397516165
PheGenIrs397516165
hapmaprs397516165
1000 genomesrs397516165
hgdprs397516165
ensemblrs397516165
gopubmedrs397516165
geneviewrs397516165
scholarrs397516165
googlers397516165
pharmgkbrs397516165
gwascentralrs397516165
openSNPrs397516165
23andMers397516165
23andMe allrs397516165
SNP Nexus

SNPshotrs397516165
SNPdbers397516165
MSV3drs397516165
GWAS Ctlgrs397516165
Max Magnitude0
ClinVar
Risk rs397516165(A;A)
Alt rs397516165(A;A)
Reference rs397516165(G;G)
Significance Probable-Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23893327C>T
CLNSRC ClinVar
CLNACC RCV000035816.2, RCV000208309.1,