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rs397516122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516122(A;A)
Make rs397516122(A;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position23427682
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516122
ebirs397516122
HLIrs397516122
Exacrs397516122
Varsomers397516122
Maprs397516122
PheGenIrs397516122
hapmaprs397516122
1000 genomesrs397516122
hgdprs397516122
ensemblrs397516122
gopubmedrs397516122
geneviewrs397516122
scholarrs397516122
googlers397516122
pharmgkbrs397516122
gwascentralrs397516122
openSNPrs397516122
23andMers397516122
23andMe allrs397516122
SNP Nexus

SNPshotrs397516122
SNPdbers397516122
MSV3drs397516122
GWAS Ctlgrs397516122
Max Magnitude0
ClinVar
Risk rs397516122(A;A)
Alt rs397516122(A;A)
Reference rs397516122(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23896891G>T
CLNSRC ClinVar
CLNACC RCV000035748.4,