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rs397516211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516211(A;A)
Make rs397516211(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23417508
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs397516211
ebirs397516211
HLIrs397516211
Exacrs397516211
Varsomers397516211
Maprs397516211
PheGenIrs397516211
hapmaprs397516211
1000 genomesrs397516211
hgdprs397516211
ensemblrs397516211
gopubmedrs397516211
geneviewrs397516211
scholarrs397516211
googlers397516211
pharmgkbrs397516211
gwascentralrs397516211
openSNPrs397516211
23andMers397516211
23andMe allrs397516211
SNP Nexus

SNPshotrs397516211
SNPdbers397516211
MSV3drs397516211
GWAS Ctlgrs397516211
Max Magnitude0
ClinVar
Risk rs397516211(A;A)
Alt rs397516211(A;A)
Reference rs397516211(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23886717C>T
CLNSRC ClinVar
CLNACC RCV000035903.3,