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rs397516103

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516103(C;C)
Make rs397516103(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23428992
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516103
ebirs397516103
HLIrs397516103
Exacrs397516103
Varsomers397516103
Maprs397516103
PheGenIrs397516103
hapmaprs397516103
1000 genomesrs397516103
hgdprs397516103
ensemblrs397516103
gopubmedrs397516103
geneviewrs397516103
scholarrs397516103
googlers397516103
pharmgkbrs397516103
gwascentralrs397516103
openSNPrs397516103
23andMers397516103
23andMe allrs397516103
SNP Nexus

SNPshotrs397516103
SNPdbers397516103
MSV3drs397516103
GWAS Ctlgrs397516103
Max Magnitude0
ClinVar
Risk rs397516103(C;C)
Alt rs397516103(C;C)
Reference rs397516103(T;T)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23898201A>G
CLNSRC ClinVar
CLNACC RCV000035720.3,