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rs267607155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607155(C;C)
Make rs267607155(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178782980
GeneTTN
is asnp
is mentioned by
dbSNPrs267607155
ebirs267607155
HLIrs267607155
Exacrs267607155
Varsomers267607155
Maprs267607155
PheGenIrs267607155
hapmaprs267607155
1000 genomesrs267607155
hgdprs267607155
ensemblrs267607155
gopubmedrs267607155
geneviewrs267607155
scholarrs267607155
googlers267607155
pharmgkbrs267607155
gwascentralrs267607155
openSNPrs267607155
23andMers267607155
23andMe allrs267607155
SNP Nexus

SNPshotrs267607155
SNPdbers267607155
MSV3drs267607155
GWAS Ctlgrs267607155
Max Magnitude0
ClinVar
Risk rs267607155(A,C;A,C)
Alt rs267607155(A,C;A,C)
Reference rs267607155(T;T)
Significance Pathogenic
Disease Dilated cardiomyopathy 1G Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Dilated cardiomyopathy 1G Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179647707A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013486.25, RCV000211871.1,