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rs869312118

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312118(C;T)
Make rs869312118(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178562617
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312118
ebirs869312118
HLIrs869312118
Exacrs869312118
Varsomers869312118
Maprs869312118
PheGenIrs869312118
hapmaprs869312118
1000 genomesrs869312118
hgdprs869312118
ensemblrs869312118
gopubmedrs869312118
geneviewrs869312118
scholarrs869312118
googlers869312118
pharmgkbrs869312118
gwascentralrs869312118
openSNPrs869312118
23andMers869312118
23andMe allrs869312118
SNP Nexus

SNPshotrs869312118
SNPdbers869312118
MSV3drs869312118
GWAS Ctlgrs869312118
Max Magnitude0
ClinVar
Risk rs869312118(T;T)
Alt rs869312118(T;T)
Reference rs869312118(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179427344G>A
CLNSRC
CLNACC RCV000208903.1,