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rs397516177

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516177(A;G)
Make rs397516177(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23423563
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516177
ebirs397516177
HLIrs397516177
Exacrs397516177
Varsomers397516177
Maprs397516177
PheGenIrs397516177
hapmaprs397516177
1000 genomesrs397516177
hgdprs397516177
ensemblrs397516177
gopubmedrs397516177
geneviewrs397516177
scholarrs397516177
googlers397516177
pharmgkbrs397516177
gwascentralrs397516177
openSNPrs397516177
23andMers397516177
23andMe allrs397516177
SNP Nexus

SNPshotrs397516177
SNPdbers397516177
MSV3drs397516177
GWAS Ctlgrs397516177
Max Magnitude0
ClinVar
Risk rs397516177(G;G)
Alt rs397516177(G;G)
Reference rs397516177(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23892772T>C
CLNSRC ClinVar
CLNACC RCV000035840.3,