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rs267607158

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607158(C;T)
Make rs267607158(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178740125
GeneTTN
is asnp
is mentioned by
dbSNPrs267607158
ebirs267607158
HLIrs267607158
Exacrs267607158
Varsomers267607158
Maprs267607158
PheGenIrs267607158
hapmaprs267607158
1000 genomesrs267607158
hgdprs267607158
ensemblrs267607158
gopubmedrs267607158
geneviewrs267607158
scholarrs267607158
googlers267607158
pharmgkbrs267607158
gwascentralrs267607158
openSNPrs267607158
23andMers267607158
23andMe allrs267607158
SNP Nexus

SNPshotrs267607158
SNPdbers267607158
MSV3drs267607158
GWAS Ctlgrs267607158
Max Magnitude0
ClinVar
Risk rs267607158(T;T)
Alt rs267607158(T;T)
Reference rs267607158(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN
CLNDBN Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179604852G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013493.17,