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rs397516187

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516187(A;A)
Make rs397516187(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23419993
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516187
ebirs397516187
HLIrs397516187
Exacrs397516187
Varsomers397516187
Maprs397516187
PheGenIrs397516187
hapmaprs397516187
1000 genomesrs397516187
hgdprs397516187
ensemblrs397516187
gopubmedrs397516187
geneviewrs397516187
scholarrs397516187
googlers397516187
pharmgkbrs397516187
gwascentralrs397516187
openSNPrs397516187
23andMers397516187
23andMe allrs397516187
SNP Nexus

SNPshotrs397516187
SNPdbers397516187
MSV3drs397516187
GWAS Ctlgrs397516187
Max Magnitude0
ClinVar
Risk rs397516187(A;A)
Alt rs397516187(A;A)
Reference rs397516187(G;G)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7 MIR208B
CLNDBN Primary dilated cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23889202C>T
CLNSRC ClinVar
CLNACC RCV000035858.3, RCV000158611.1, RCV000168889.1,