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rs397516128

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516128(C;C)
Make rs397516128(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23426057
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516128
ebirs397516128
HLIrs397516128
Exacrs397516128
Varsomers397516128
Maprs397516128
PheGenIrs397516128
hapmaprs397516128
1000 genomesrs397516128
hgdprs397516128
ensemblrs397516128
gopubmedrs397516128
geneviewrs397516128
scholarrs397516128
googlers397516128
pharmgkbrs397516128
gwascentralrs397516128
openSNPrs397516128
23andMers397516128
23andMe allrs397516128
SNP Nexus

SNPshotrs397516128
SNPdbers397516128
MSV3drs397516128
GWAS Ctlgrs397516128
Max Magnitude0
ClinVar
Risk rs397516128(C;C)
Alt rs397516128(C;C)
Reference rs397516128(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23895266A>G
CLNSRC ClinVar
CLNACC RCV000035759.3,