Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025552

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025552(-;-)
Make rs869025552(-;T)
Make rs869025552(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178602411
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025552
ebirs869025552
HLIrs869025552
Exacrs869025552
Varsomers869025552
Maprs869025552
PheGenIrs869025552
hapmaprs869025552
1000 genomesrs869025552
hgdprs869025552
ensemblrs869025552
gopubmedrs869025552
geneviewrs869025552
scholarrs869025552
googlers869025552
pharmgkbrs869025552
gwascentralrs869025552
openSNPrs869025552
23andMers869025552
23andMe allrs869025552
SNP Nexus

SNPshotrs869025552
SNPdbers869025552
MSV3drs869025552
GWAS Ctlgrs869025552
Max Magnitude0
ClinVar
Risk rs869025552(T;T)
Alt rs869025552(T;T)
Reference rs869025552(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179467139dupA
CLNSRC
CLNACC RCV000208341.1,