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rs397516268

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516268(A;G)
Make rs397516268(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431466
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516268
ebirs397516268
HLIrs397516268
Exacrs397516268
Varsomers397516268
Maprs397516268
PheGenIrs397516268
hapmaprs397516268
1000 genomesrs397516268
hgdprs397516268
ensemblrs397516268
gopubmedrs397516268
geneviewrs397516268
scholarrs397516268
googlers397516268
pharmgkbrs397516268
gwascentralrs397516268
openSNPrs397516268
23andMers397516268
23andMe allrs397516268
SNP Nexus

SNPshotrs397516268
SNPdbers397516268
MSV3drs397516268
GWAS Ctlgrs397516268
Max Magnitude0
ClinVar
Risk rs397516268(G,T;G,T)
Alt rs397516268(G,T;G,T)
Reference rs397516268(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23900675T>A; NC_000014.8:g.23900675T>C
CLNSRC
CLNACC RCV000158762.1, RCV000036001.3,