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rs869025553

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025553(-;-)
Make rs869025553(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178569759
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025553
ebirs869025553
HLIrs869025553
Exacrs869025553
Varsomers869025553
Maprs869025553
PheGenIrs869025553
hapmaprs869025553
1000 genomesrs869025553
hgdprs869025553
ensemblrs869025553
gopubmedrs869025553
geneviewrs869025553
scholarrs869025553
googlers869025553
pharmgkbrs869025553
gwascentralrs869025553
openSNPrs869025553
23andMers869025553
23andMe allrs869025553
SNP Nexus

SNPshotrs869025553
SNPdbers869025553
MSV3drs869025553
GWAS Ctlgrs869025553
Max Magnitude0
ClinVar
Risk rs869025553(;)
Alt rs869025553(;)
Reference rs869025553(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179434486delG
CLNSRC
CLNACC RCV000208486.1,