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rs397516259

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516259(A;A)
Make rs397516259(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431790
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516259
ebirs397516259
HLIrs397516259
Exacrs397516259
Varsomers397516259
Maprs397516259
PheGenIrs397516259
hapmaprs397516259
1000 genomesrs397516259
hgdprs397516259
ensemblrs397516259
gopubmedrs397516259
geneviewrs397516259
scholarrs397516259
googlers397516259
pharmgkbrs397516259
gwascentralrs397516259
openSNPrs397516259
23andMers397516259
23andMe allrs397516259
SNP Nexus

SNPshotrs397516259
SNPdbers397516259
MSV3drs397516259
GWAS Ctlgrs397516259
Max Magnitude0
ClinVar
Risk rs397516259(A,T;A,T)
Alt rs397516259(A,T;A,T)
Reference rs397516259(C;C)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23900999G>A; NC_000014.8:g.23900999G>T
CLNSRC
CLNACC RCV000158748.1, RCV000035989.3,