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rs869312113

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs869312113(-;-)
Make rs869312113(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178576752
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312113
ebirs869312113
HLIrs869312113
Exacrs869312113
Varsomers869312113
Maprs869312113
PheGenIrs869312113
hapmaprs869312113
1000 genomesrs869312113
hgdprs869312113
ensemblrs869312113
gopubmedrs869312113
geneviewrs869312113
scholarrs869312113
googlers869312113
pharmgkbrs869312113
gwascentralrs869312113
openSNPrs869312113
23andMers869312113
23andMe allrs869312113
SNP Nexus

SNPshotrs869312113
SNPdbers869312113
MSV3drs869312113
GWAS Ctlgrs869312113
Max Magnitude0
ClinVar
Risk rs869312113(;)
Alt rs869312113(;)
Reference rs869312113(TG;TG)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179441479_179441480delCA
CLNSRC
CLNACC RCV000209039.1,