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rs397516207

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516207(A;A)
Make rs397516207(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417597
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516207
ebirs397516207
HLIrs397516207
Exacrs397516207
Varsomers397516207
Maprs397516207
PheGenIrs397516207
hapmaprs397516207
1000 genomesrs397516207
hgdprs397516207
ensemblrs397516207
gopubmedrs397516207
geneviewrs397516207
scholarrs397516207
googlers397516207
pharmgkbrs397516207
gwascentralrs397516207
openSNPrs397516207
23andMers397516207
23andMe allrs397516207
SNP Nexus

SNPshotrs397516207
SNPdbers397516207
MSV3drs397516207
GWAS Ctlgrs397516207
Max Magnitude0
ClinVar
Risk rs397516207(A;A)
Alt rs397516207(A;A)
Reference rs397516207(G;G)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not specified Hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23886806C>T
CLNSRC
CLNACC RCV000035898.2, RCV000200190.1, RCV000225723.1,