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rs397516141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516141(A;C)
Make rs397516141(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position23425409
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516141
ebirs397516141
HLIrs397516141
Exacrs397516141
Varsomers397516141
Maprs397516141
PheGenIrs397516141
hapmaprs397516141
1000 genomesrs397516141
hgdprs397516141
ensemblrs397516141
gopubmedrs397516141
geneviewrs397516141
scholarrs397516141
googlers397516141
pharmgkbrs397516141
gwascentralrs397516141
openSNPrs397516141
23andMers397516141
23andMe allrs397516141
SNP Nexus

SNPshotrs397516141
SNPdbers397516141
MSV3drs397516141
GWAS Ctlgrs397516141
Max Magnitude0
ClinVar
Risk rs397516141(C;C)
Alt rs397516141(C;C)
Reference rs397516141(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23894618T>G
CLNSRC ClinVar
CLNACC RCV000035782.4,