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rs869312055

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312055(C;T)
Make rs869312055(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178590794
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312055
ebirs869312055
HLIrs869312055
Exacrs869312055
Varsomers869312055
Maprs869312055
PheGenIrs869312055
hapmaprs869312055
1000 genomesrs869312055
hgdprs869312055
ensemblrs869312055
gopubmedrs869312055
geneviewrs869312055
scholarrs869312055
googlers869312055
pharmgkbrs869312055
gwascentralrs869312055
openSNPrs869312055
23andMers869312055
23andMe allrs869312055
SNP Nexus

SNPshotrs869312055
SNPdbers869312055
MSV3drs869312055
GWAS Ctlgrs869312055
Max Magnitude0
ClinVar
Risk rs869312055(T;T)
Alt rs869312055(T;T)
Reference rs869312055(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.179455521G>A
CLNSRC
CLNACC RCV000209305.1,