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rs869312066

From SNPedia

Orientationminus
Geno Mag Summary
(GCCCGAT;GCCCGAT) 0 common in clinvar
Make rs869312066(-;-)
Make rs869312066(-;GCCCGAT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178546473
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312066
ebirs869312066
HLIrs869312066
Exacrs869312066
Varsomers869312066
Maprs869312066
PheGenIrs869312066
hapmaprs869312066
1000 genomesrs869312066
hgdprs869312066
ensemblrs869312066
gopubmedrs869312066
geneviewrs869312066
scholarrs869312066
googlers869312066
pharmgkbrs869312066
gwascentralrs869312066
openSNPrs869312066
23andMers869312066
23andMe allrs869312066
SNP Nexus

SNPshotrs869312066
SNPdbers869312066
MSV3drs869312066
GWAS Ctlgrs869312066
Max Magnitude0
ClinVar
Risk rs869312066(;)
Alt rs869312066(;)
Reference rs869312066(GCCCGAT;GCCCGAT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179411200_179411206delATCGGGC
CLNSRC
CLNACC RCV000208924.1,