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rs397516238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516238(A;T)
Make rs397516238(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23432502
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516238
ebirs397516238
HLIrs397516238
Exacrs397516238
Varsomers397516238
Maprs397516238
PheGenIrs397516238
hapmaprs397516238
1000 genomesrs397516238
hgdprs397516238
ensemblrs397516238
gopubmedrs397516238
geneviewrs397516238
scholarrs397516238
googlers397516238
pharmgkbrs397516238
gwascentralrs397516238
openSNPrs397516238
23andMers397516238
23andMe allrs397516238
SNP Nexus

SNPshotrs397516238
SNPdbers397516238
MSV3drs397516238
GWAS Ctlgrs397516238
Max Magnitude0
ClinVar
Risk rs397516238(T;T)
Alt rs397516238(T;T)
Reference rs397516238(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901711T>A
CLNSRC ClinVar
CLNACC RCV000035949.3,