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rs869312054

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312054(C;C)
Make rs869312054(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178593566
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312054
ebirs869312054
HLIrs869312054
Exacrs869312054
Varsomers869312054
Maprs869312054
PheGenIrs869312054
hapmaprs869312054
1000 genomesrs869312054
hgdprs869312054
ensemblrs869312054
gopubmedrs869312054
geneviewrs869312054
scholarrs869312054
googlers869312054
pharmgkbrs869312054
gwascentralrs869312054
openSNPrs869312054
23andMers869312054
23andMe allrs869312054
SNP Nexus

SNPshotrs869312054
SNPdbers869312054
MSV3drs869312054
GWAS Ctlgrs869312054
Max Magnitude0
ClinVar
Risk rs869312054(C;C)
Alt rs869312054(C;C)
Reference rs869312054(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.179458293A>G
CLNSRC
CLNACC RCV000208977.1,