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rs397516199

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516199(C;T)
Make rs397516199(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23418375
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516199
ebirs397516199
HLIrs397516199
Exacrs397516199
Varsomers397516199
Maprs397516199
PheGenIrs397516199
hapmaprs397516199
1000 genomesrs397516199
hgdprs397516199
ensemblrs397516199
gopubmedrs397516199
geneviewrs397516199
scholarrs397516199
googlers397516199
pharmgkbrs397516199
gwascentralrs397516199
openSNPrs397516199
23andMers397516199
23andMe allrs397516199
SNP Nexus

SNPshotrs397516199
SNPdbers397516199
MSV3drs397516199
GWAS Ctlgrs397516199
Max Magnitude0
ClinVar
Risk rs397516199(T;T)
Alt rs397516199(T;T)
Reference rs397516199(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23887584G>A
CLNSRC ClinVar
CLNACC RCV000035881.3,