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rs397516275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516275(A;A)
Make rs397516275(A;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23430591
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516275
ebirs397516275
HLIrs397516275
Exacrs397516275
Varsomers397516275
Maprs397516275
PheGenIrs397516275
hapmaprs397516275
1000 genomesrs397516275
hgdprs397516275
ensemblrs397516275
gopubmedrs397516275
geneviewrs397516275
scholarrs397516275
googlers397516275
pharmgkbrs397516275
gwascentralrs397516275
openSNPrs397516275
23andMers397516275
23andMe allrs397516275
SNP Nexus

SNPshotrs397516275
SNPdbers397516275
MSV3drs397516275
GWAS Ctlgrs397516275
Max Magnitude0
ClinVar
Risk rs397516275(A,C,G;A,C,G)
Alt rs397516275(A,C,G;A,C,G)
Reference rs397516275(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23899800A>G; NC_000014.8:g.23899800A>T
CLNSRC ClinVar
CLNACC RCV000036013.3, RCV000036012.4,