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rs869312058

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312058(-;-)
Make rs869312058(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178567625
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312058
ebirs869312058
HLIrs869312058
Exacrs869312058
Varsomers869312058
Maprs869312058
PheGenIrs869312058
hapmaprs869312058
1000 genomesrs869312058
hgdprs869312058
ensemblrs869312058
gopubmedrs869312058
geneviewrs869312058
scholarrs869312058
googlers869312058
pharmgkbrs869312058
gwascentralrs869312058
openSNPrs869312058
23andMers869312058
23andMe allrs869312058
SNP Nexus

SNPshotrs869312058
SNPdbers869312058
MSV3drs869312058
GWAS Ctlgrs869312058
Max Magnitude0
ClinVar
Risk rs869312058(;)
Alt rs869312058(;)
Reference rs869312058(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179432352delA
CLNSRC
CLNACC RCV000209036.1,