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

rs869025554

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025554(-;-)
Make rs869025554(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178557413
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025554
ebirs869025554
HLIrs869025554
Exacrs869025554
Varsomers869025554
Maprs869025554
PheGenIrs869025554
hapmaprs869025554
1000 genomesrs869025554
hgdprs869025554
ensemblrs869025554
gopubmedrs869025554
geneviewrs869025554
scholarrs869025554
googlers869025554
pharmgkbrs869025554
gwascentralrs869025554
openSNPrs869025554
23andMers869025554
23andMe allrs869025554
SNP Nexus

SNPshotrs869025554
SNPdbers869025554
MSV3drs869025554
GWAS Ctlgrs869025554
Max Magnitude0
ClinVar
Risk rs869025554(;)
Alt rs869025554(;)
Reference rs869025554(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179422140delT
CLNSRC
CLNACC RCV000208165.1,