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rs397516106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516106(G;T)
Make rs397516106(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23428957
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516106
ebirs397516106
HLIrs397516106
Exacrs397516106
Varsomers397516106
Maprs397516106
PheGenIrs397516106
hapmaprs397516106
1000 genomesrs397516106
hgdprs397516106
ensemblrs397516106
gopubmedrs397516106
geneviewrs397516106
scholarrs397516106
googlers397516106
pharmgkbrs397516106
gwascentralrs397516106
openSNPrs397516106
23andMers397516106
23andMe allrs397516106
SNP Nexus

SNPshotrs397516106
SNPdbers397516106
MSV3drs397516106
GWAS Ctlgrs397516106
Max Magnitude0
ClinVar
Risk rs397516106(A,T;A,T)
Alt rs397516106(A,T;A,T)
Reference rs397516106(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23898166C>A; NC_000014.8:g.23898166C>T
CLNSRC ClinVar
CLNACC RCV000035724.3, RCV000154581.2,