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rs397516138

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516138(A;G)
Make rs397516138(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425775
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516138
ebirs397516138
HLIrs397516138
Exacrs397516138
Varsomers397516138
Maprs397516138
PheGenIrs397516138
hapmaprs397516138
1000 genomesrs397516138
hgdprs397516138
ensemblrs397516138
gopubmedrs397516138
geneviewrs397516138
scholarrs397516138
googlers397516138
pharmgkbrs397516138
gwascentralrs397516138
openSNPrs397516138
23andMers397516138
23andMe allrs397516138
SNP Nexus

SNPshotrs397516138
SNPdbers397516138
MSV3drs397516138
GWAS Ctlgrs397516138
Max Magnitude0
ClinVar
Risk rs397516138(G;G)
Alt rs397516138(G;G)
Reference rs397516138(A;A)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1 not provided
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1 not provided
Reversed 1
HGVS NC_000014.8:g.23894984T>C
CLNSRC
CLNACC RCV000035777.2, RCV000185533.2, RCV000225741.1,