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rs869312079

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312079(-;-)
Make rs869312079(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178564614
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312079
ebirs869312079
HLIrs869312079
Exacrs869312079
Varsomers869312079
Maprs869312079
PheGenIrs869312079
hapmaprs869312079
1000 genomesrs869312079
hgdprs869312079
ensemblrs869312079
gopubmedrs869312079
geneviewrs869312079
scholarrs869312079
googlers869312079
pharmgkbrs869312079
gwascentralrs869312079
openSNPrs869312079
23andMers869312079
23andMe allrs869312079
SNP Nexus

SNPshotrs869312079
SNPdbers869312079
MSV3drs869312079
GWAS Ctlgrs869312079
Max Magnitude0
ClinVar
Risk rs869312079(;)
Alt rs869312079(;)
Reference rs869312079(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.179429341delG
CLNSRC
CLNACC RCV000208927.1,