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rs149576470

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149576470(A;A)
Make rs149576470(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424863
GeneMYH7
is asnp
is mentioned by
dbSNPrs149576470
ebirs149576470
HLIrs149576470
Exacrs149576470
Varsomers149576470
Maprs149576470
PheGenIrs149576470
hapmaprs149576470
1000 genomesrs149576470
hgdprs149576470
ensemblrs149576470
gopubmedrs149576470
geneviewrs149576470
scholarrs149576470
googlers149576470
pharmgkbrs149576470
gwascentralrs149576470
openSNPrs149576470
23andMers149576470
23andMe allrs149576470
SNP Nexus

SNPshotrs149576470
SNPdbers149576470
MSV3drs149576470
GWAS Ctlgrs149576470
Max Magnitude0
ClinVar
Risk rs149576470(A;A)
Alt rs149576470(A;A)
Reference rs149576470(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23894072G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030314.1,