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rs397516227

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516227(C;T)
Make rs397516227(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23416237
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516227
ebirs397516227
HLIrs397516227
Exacrs397516227
Varsomers397516227
Maprs397516227
PheGenIrs397516227
hapmaprs397516227
1000 genomesrs397516227
hgdprs397516227
ensemblrs397516227
gopubmedrs397516227
geneviewrs397516227
scholarrs397516227
googlers397516227
pharmgkbrs397516227
gwascentralrs397516227
openSNPrs397516227
23andMers397516227
23andMe allrs397516227
SNP Nexus

SNPshotrs397516227
SNPdbers397516227
MSV3drs397516227
GWAS Ctlgrs397516227
Max Magnitude0
ClinVar
Risk rs397516227(T;T)
Alt rs397516227(T;T)
Reference rs397516227(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23885446G>A
CLNSRC ClinVar
CLNACC RCV000035927.3,