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rs377491278

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377491278(C;T)
Make rs377491278(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23427773
GeneMYH7
is asnp
is mentioned by
dbSNPrs377491278
ebirs377491278
HLIrs377491278
Exacrs377491278
Varsomers377491278
Maprs377491278
PheGenIrs377491278
hapmaprs377491278
1000 genomesrs377491278
hgdprs377491278
ensemblrs377491278
gopubmedrs377491278
geneviewrs377491278
scholarrs377491278
googlers377491278
pharmgkbrs377491278
gwascentralrs377491278
openSNPrs377491278
23andMers377491278
23andMe allrs377491278
SNP Nexus

SNPshotrs377491278
SNPdbers377491278
MSV3drs377491278
GWAS Ctlgrs377491278
Max Magnitude0
ClinVar
Risk rs377491278(T;T)
Alt rs377491278(T;T)
Reference rs377491278(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23896982C>T
CLNSRC ClinVar
CLNACC RCV000035741.3,