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rs397516208

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516208(A;A)
Make rs397516208(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23417580
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516208
ebirs397516208
HLIrs397516208
Exacrs397516208
Varsomers397516208
Maprs397516208
PheGenIrs397516208
hapmaprs397516208
1000 genomesrs397516208
hgdprs397516208
ensemblrs397516208
gopubmedrs397516208
geneviewrs397516208
scholarrs397516208
googlers397516208
pharmgkbrs397516208
gwascentralrs397516208
openSNPrs397516208
23andMers397516208
23andMe allrs397516208
SNP Nexus

SNPshotrs397516208
SNPdbers397516208
MSV3drs397516208
GWAS Ctlgrs397516208
Max Magnitude0
ClinVar
Risk rs397516208(A;A)
Alt rs397516208(A;A)
Reference rs397516208(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23886789C>T
CLNSRC ClinVar
CLNACC RCV000035899.3,