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rs397516186

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516186(A;A)
Make rs397516186(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23420107
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516186
ebirs397516186
HLIrs397516186
Exacrs397516186
Varsomers397516186
Maprs397516186
PheGenIrs397516186
hapmaprs397516186
1000 genomesrs397516186
hgdprs397516186
ensemblrs397516186
gopubmedrs397516186
geneviewrs397516186
scholarrs397516186
googlers397516186
pharmgkbrs397516186
gwascentralrs397516186
openSNPrs397516186
23andMers397516186
23andMe allrs397516186
SNP Nexus

SNPshotrs397516186
SNPdbers397516186
MSV3drs397516186
GWAS Ctlgrs397516186
Max Magnitude0
ClinVar
Risk rs397516186(A;A)
Alt rs397516186(A;A)
Reference rs397516186(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23889316C>T
CLNSRC ClinVar
CLNACC RCV000035857.4,