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rs267607157

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607157(C;T)
Make rs267607157(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178785990
GeneTTN
is asnp
is mentioned by
dbSNPrs267607157
ebirs267607157
HLIrs267607157
Exacrs267607157
Varsomers267607157
Maprs267607157
PheGenIrs267607157
hapmaprs267607157
1000 genomesrs267607157
hgdprs267607157
ensemblrs267607157
gopubmedrs267607157
geneviewrs267607157
scholarrs267607157
googlers267607157
pharmgkbrs267607157
gwascentralrs267607157
openSNPrs267607157
23andMers267607157
23andMe allrs267607157
SNP Nexus

SNPshotrs267607157
SNPdbers267607157
MSV3drs267607157
GWAS Ctlgrs267607157
Max Magnitude0
ClinVar
Risk rs267607157(T;T)
Alt rs267607157(T;T)
Reference rs267607157(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN
CLNDBN Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179650717G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013491.17,