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rs397516182

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516182(A;A)
Make rs397516182(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419934
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516182
ebirs397516182
HLIrs397516182
Exacrs397516182
Varsomers397516182
Maprs397516182
PheGenIrs397516182
hapmaprs397516182
1000 genomesrs397516182
hgdprs397516182
ensemblrs397516182
gopubmedrs397516182
geneviewrs397516182
scholarrs397516182
googlers397516182
pharmgkbrs397516182
gwascentralrs397516182
openSNPrs397516182
23andMers397516182
23andMe allrs397516182
SNP Nexus

SNPshotrs397516182
SNPdbers397516182
MSV3drs397516182
GWAS Ctlgrs397516182
Max Magnitude0
ClinVar
Risk rs397516182(A;A)
Alt rs397516182(A;A)
Reference rs397516182(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23889143C>T
CLNSRC
CLNACC RCV000035851.2, RCV000158618.1,