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rs397516183

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516183(C;C)
Make rs397516183(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23433086
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516183
ebirs397516183
HLIrs397516183
Exacrs397516183
Varsomers397516183
Maprs397516183
PheGenIrs397516183
hapmaprs397516183
1000 genomesrs397516183
hgdprs397516183
ensemblrs397516183
gopubmedrs397516183
geneviewrs397516183
scholarrs397516183
googlers397516183
pharmgkbrs397516183
gwascentralrs397516183
openSNPrs397516183
23andMers397516183
23andMe allrs397516183
SNP Nexus

SNPshotrs397516183
SNPdbers397516183
MSV3drs397516183
GWAS Ctlgrs397516183
Max Magnitude0
ClinVar
Risk rs397516183(C;C)
Alt rs397516183(C;C)
Reference rs397516183(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23902295A>G
CLNSRC ClinVar
CLNACC RCV000035853.4,