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rs869312069

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312069(-;-)
Make rs869312069(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178529122
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312069
ebirs869312069
HLIrs869312069
Exacrs869312069
Varsomers869312069
Maprs869312069
PheGenIrs869312069
hapmaprs869312069
1000 genomesrs869312069
hgdprs869312069
ensemblrs869312069
gopubmedrs869312069
geneviewrs869312069
scholarrs869312069
googlers869312069
pharmgkbrs869312069
gwascentralrs869312069
openSNPrs869312069
23andMers869312069
23andMe allrs869312069
SNP Nexus

SNPshotrs869312069
SNPdbers869312069
MSV3drs869312069
GWAS Ctlgrs869312069
Max Magnitude0
ClinVar
Risk rs869312069(;)
Alt rs869312069(;)
Reference rs869312069(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179393849delT
CLNSRC
CLNACC RCV000209272.1,