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rs397516249

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516249(A;G)
Make rs397516249(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23431840
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516249
ebirs397516249
HLIrs397516249
Exacrs397516249
Varsomers397516249
Maprs397516249
PheGenIrs397516249
hapmaprs397516249
1000 genomesrs397516249
hgdprs397516249
ensemblrs397516249
gopubmedrs397516249
geneviewrs397516249
scholarrs397516249
googlers397516249
pharmgkbrs397516249
gwascentralrs397516249
openSNPrs397516249
23andMers397516249
23andMe allrs397516249
SNP Nexus

SNPshotrs397516249
SNPdbers397516249
MSV3drs397516249
GWAS Ctlgrs397516249
Max Magnitude0
ClinVar
Risk rs397516249(G;G)
Alt rs397516249(G;G)
Reference rs397516249(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23901049T>C
CLNSRC ClinVar
CLNACC RCV000035972.3,