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rs397516120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516120(A;G)
Make rs397516120(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23427731
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516120
ebirs397516120
HLIrs397516120
Exacrs397516120
Varsomers397516120
Maprs397516120
PheGenIrs397516120
hapmaprs397516120
1000 genomesrs397516120
hgdprs397516120
ensemblrs397516120
gopubmedrs397516120
geneviewrs397516120
scholarrs397516120
googlers397516120
pharmgkbrs397516120
gwascentralrs397516120
openSNPrs397516120
23andMers397516120
23andMe allrs397516120
SNP Nexus

SNPshotrs397516120
SNPdbers397516120
MSV3drs397516120
GWAS Ctlgrs397516120
Max Magnitude0
ClinVar
Risk rs397516120(G;G)
Alt rs397516120(G;G)
Reference rs397516120(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23896940T>C
CLNSRC ClinVar
CLNACC RCV000035742.3,