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rs869025559

From SNPedia

Orientationminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs869025559(-;-)
Make rs869025559(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178562342
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025559
ebirs869025559
HLIrs869025559
Exacrs869025559
Varsomers869025559
Maprs869025559
PheGenIrs869025559
hapmaprs869025559
1000 genomesrs869025559
hgdprs869025559
ensemblrs869025559
gopubmedrs869025559
geneviewrs869025559
scholarrs869025559
googlers869025559
pharmgkbrs869025559
gwascentralrs869025559
openSNPrs869025559
23andMers869025559
23andMe allrs869025559
SNP Nexus

SNPshotrs869025559
SNPdbers869025559
MSV3drs869025559
GWAS Ctlgrs869025559
Max Magnitude0
ClinVar
Risk rs869025559(;)
Alt rs869025559(;)
Reference rs869025559(AA;AA)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179427069_179427070delTT
CLNSRC
CLNACC RCV000208049.1,