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rs869025549

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025549(A;G)
Make rs869025549(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178583229
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025549
ebirs869025549
HLIrs869025549
Exacrs869025549
Varsomers869025549
Maprs869025549
PheGenIrs869025549
hapmaprs869025549
1000 genomesrs869025549
hgdprs869025549
ensemblrs869025549
gopubmedrs869025549
geneviewrs869025549
scholarrs869025549
googlers869025549
pharmgkbrs869025549
gwascentralrs869025549
openSNPrs869025549
23andMers869025549
23andMe allrs869025549
SNP Nexus

SNPshotrs869025549
SNPdbers869025549
MSV3drs869025549
GWAS Ctlgrs869025549
Max Magnitude0
ClinVar
Risk rs869025549(G;G)
Alt rs869025549(G;G)
Reference rs869025549(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.179447956T>C
CLNSRC
CLNACC RCV000208314.1,