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rs150415679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150415679(C;T)
Make rs150415679(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position23398866
GeneMYH6
is asnp
is mentioned by
dbSNPrs150415679
ebirs150415679
HLIrs150415679
Exacrs150415679
Varsomers150415679
Maprs150415679
PheGenIrs150415679
hapmaprs150415679
1000 genomesrs150415679
hgdprs150415679
ensemblrs150415679
gopubmedrs150415679
geneviewrs150415679
scholarrs150415679
googlers150415679
pharmgkbrs150415679
gwascentralrs150415679
openSNPrs150415679
23andMers150415679
23andMe allrs150415679
SNP Nexus

SNPshotrs150415679
SNPdbers150415679
MSV3drs150415679
GWAS Ctlgrs150415679
Max Magnitude0
ClinVar
Risk rs150415679(T;T)
Alt rs150415679(T;T)
Reference rs150415679(C;C)
Significance Probable-non-pathogenic
Disease Cardiomyopathy not specified
Variation info
Gene MYH6
CLNDBN Cardiomyopathy not specified
Reversed 0
HGVS NC_000014.8:g.23868075C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030305.1, RCV000037446.2,