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rs869312063

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312063(-;-)
Make rs869312063(-;G)
Make rs869312063(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178553149
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312063
ebirs869312063
HLIrs869312063
Exacrs869312063
Varsomers869312063
Maprs869312063
PheGenIrs869312063
hapmaprs869312063
1000 genomesrs869312063
hgdprs869312063
ensemblrs869312063
gopubmedrs869312063
geneviewrs869312063
scholarrs869312063
googlers869312063
pharmgkbrs869312063
gwascentralrs869312063
openSNPrs869312063
23andMers869312063
23andMe allrs869312063
SNP Nexus

SNPshotrs869312063
SNPdbers869312063
MSV3drs869312063
GWAS Ctlgrs869312063
Max Magnitude0
ClinVar
Risk rs869312063(G;G)
Alt rs869312063(G;G)
Reference rs869312063(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179417877dupC
CLNSRC
CLNACC RCV000209730.1,