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rs397516201

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516201(C;T)
Make rs397516201(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418249
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516201
ebirs397516201
HLIrs397516201
Exacrs397516201
Varsomers397516201
Maprs397516201
PheGenIrs397516201
hapmaprs397516201
1000 genomesrs397516201
hgdprs397516201
ensemblrs397516201
gopubmedrs397516201
geneviewrs397516201
scholarrs397516201
googlers397516201
pharmgkbrs397516201
gwascentralrs397516201
openSNPrs397516201
23andMers397516201
23andMe allrs397516201
SNP Nexus

SNPshotrs397516201
SNPdbers397516201
MSV3drs397516201
GWAS Ctlgrs397516201
Max Magnitude0
ClinVar
Risk rs397516201(T;T)
Alt rs397516201(T;T)
Reference rs397516201(C;C)
Significance Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7 MIR208B
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23887458G>A
CLNSRC
CLNACC RCV000035886.2, RCV000208315.1,