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rs397516245

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516245(C;T)
Make rs397516245(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23415213
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516245
ebirs397516245
HLIrs397516245
Exacrs397516245
Varsomers397516245
Maprs397516245
PheGenIrs397516245
hapmaprs397516245
1000 genomesrs397516245
hgdprs397516245
ensemblrs397516245
gopubmedrs397516245
geneviewrs397516245
scholarrs397516245
googlers397516245
pharmgkbrs397516245
gwascentralrs397516245
openSNPrs397516245
23andMers397516245
23andMe allrs397516245
SNP Nexus

SNPshotrs397516245
SNPdbers397516245
MSV3drs397516245
GWAS Ctlgrs397516245
Max Magnitude0
ClinVar
Risk rs397516245(T;T)
Alt rs397516245(T;T)
Reference rs397516245(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884422G>A
CLNSRC ClinVar
CLNACC RCV000035958.3,