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rs869312085

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312085(C;T)
Make rs869312085(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178539559
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312085
ebirs869312085
HLIrs869312085
Exacrs869312085
Varsomers869312085
Maprs869312085
PheGenIrs869312085
hapmaprs869312085
1000 genomesrs869312085
hgdprs869312085
ensemblrs869312085
gopubmedrs869312085
geneviewrs869312085
scholarrs869312085
googlers869312085
pharmgkbrs869312085
gwascentralrs869312085
openSNPrs869312085
23andMers869312085
23andMe allrs869312085
SNP Nexus

SNPshotrs869312085
SNPdbers869312085
MSV3drs869312085
GWAS Ctlgrs869312085
Max Magnitude0
ClinVar
Risk rs869312085(T;T)
Alt rs869312085(T;T)
Reference rs869312085(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.179404286G>A
CLNSRC
CLNACC RCV000209446.1,