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rs869312114

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312114(G;T)
Make rs869312114(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178576255
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312114
ebirs869312114
HLIrs869312114
Exacrs869312114
Varsomers869312114
Maprs869312114
PheGenIrs869312114
hapmaprs869312114
1000 genomesrs869312114
hgdprs869312114
ensemblrs869312114
gopubmedrs869312114
geneviewrs869312114
scholarrs869312114
googlers869312114
pharmgkbrs869312114
gwascentralrs869312114
openSNPrs869312114
23andMers869312114
23andMe allrs869312114
SNP Nexus

SNPshotrs869312114
SNPdbers869312114
MSV3drs869312114
GWAS Ctlgrs869312114
Max Magnitude0
ClinVar
Risk rs869312114(T;T)
Alt rs869312114(T;T)
Reference rs869312114(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.179440982C>A
CLNSRC
CLNACC RCV000209461.1,