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rs397516178

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516178(G;T)
Make rs397516178(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23422291
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516178
ebirs397516178
HLIrs397516178
Exacrs397516178
Varsomers397516178
Maprs397516178
PheGenIrs397516178
hapmaprs397516178
1000 genomesrs397516178
hgdprs397516178
ensemblrs397516178
gopubmedrs397516178
geneviewrs397516178
scholarrs397516178
googlers397516178
pharmgkbrs397516178
gwascentralrs397516178
openSNPrs397516178
23andMers397516178
23andMe allrs397516178
SNP Nexus

SNPshotrs397516178
SNPdbers397516178
MSV3drs397516178
GWAS Ctlgrs397516178
Max Magnitude0
ClinVar
Risk rs397516178(A,T;A,T)
Alt rs397516178(A,T;A,T)
Reference rs397516178(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23891500C>A
CLNSRC ClinVar
CLNACC RCV000035841.3,