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rs397516095

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516095(G;T)
Make rs397516095(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23429266
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516095
ebirs397516095
HLIrs397516095
Exacrs397516095
Varsomers397516095
Maprs397516095
PheGenIrs397516095
hapmaprs397516095
1000 genomesrs397516095
hgdprs397516095
ensemblrs397516095
gopubmedrs397516095
geneviewrs397516095
scholarrs397516095
googlers397516095
pharmgkbrs397516095
gwascentralrs397516095
openSNPrs397516095
23andMers397516095
23andMe allrs397516095
SNP Nexus

SNPshotrs397516095
SNPdbers397516095
MSV3drs397516095
GWAS Ctlgrs397516095
Max Magnitude0
ClinVar
Risk rs397516095(T;T)
Alt rs397516095(T;T)
Reference rs397516095(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23898475C>A
CLNSRC
CLNACC RCV000035709.2,