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rs869025548

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025548(A;G)
Make rs869025548(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178620627
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025548
ebirs869025548
HLIrs869025548
Exacrs869025548
Varsomers869025548
Maprs869025548
PheGenIrs869025548
hapmaprs869025548
1000 genomesrs869025548
hgdprs869025548
ensemblrs869025548
gopubmedrs869025548
geneviewrs869025548
scholarrs869025548
googlers869025548
pharmgkbrs869025548
gwascentralrs869025548
openSNPrs869025548
23andMers869025548
23andMe allrs869025548
SNP Nexus

SNPshotrs869025548
SNPdbers869025548
MSV3drs869025548
GWAS Ctlgrs869025548
Max Magnitude0
ClinVar
Risk rs869025548(G;G)
Alt rs869025548(G;G)
Reference rs869025548(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.179485354T>C
CLNSRC
CLNACC RCV000208417.1,