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rs45516091

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45516091(C;T)
Make rs45516091(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431608
GeneMYH7
is asnp
is mentioned by
dbSNPrs45516091
ebirs45516091
HLIrs45516091
Exacrs45516091
Varsomers45516091
Maprs45516091
PheGenIrs45516091
hapmaprs45516091
1000 genomesrs45516091
hgdprs45516091
ensemblrs45516091
gopubmedrs45516091
geneviewrs45516091
scholarrs45516091
googlers45516091
pharmgkbrs45516091
gwascentralrs45516091
openSNPrs45516091
23andMers45516091
23andMe allrs45516091
SNP Nexus

SNPshotrs45516091
SNPdbers45516091
MSV3drs45516091
GWAS Ctlgrs45516091
Max Magnitude0
ClinVar
Risk rs45516091(T;T)
Alt rs45516091(T;T)
Reference Rs45516091(C;C)
Significance Other
Disease Primary dilated cardiomyopathy not provided not specified Cardiovascular phenotype
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy not provided not specified Cardiovascular phenotype
Reversed 1
HGVS NC_000014.8:g.23900817G>A
CLNSRC
CLNACC RCV000157351.2, RCV000158879.2, RCV000223687.1, RCV000252658.1,