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rs869025546

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025546(A;A)
Make rs869025546(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178555038
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025546
ebirs869025546
HLIrs869025546
Exacrs869025546
Varsomers869025546
Maprs869025546
PheGenIrs869025546
hapmaprs869025546
1000 genomesrs869025546
hgdprs869025546
ensemblrs869025546
gopubmedrs869025546
geneviewrs869025546
scholarrs869025546
googlers869025546
pharmgkbrs869025546
gwascentralrs869025546
openSNPrs869025546
23andMers869025546
23andMe allrs869025546
SNP Nexus

SNPshotrs869025546
SNPdbers869025546
MSV3drs869025546
GWAS Ctlgrs869025546
Max Magnitude0
ClinVar
Risk rs869025546(A;A)
Alt rs869025546(A;A)
Reference rs869025546(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179419765C>T
CLNSRC
CLNACC RCV000208359.1,