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rs869312067

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312067(-;-)
Make rs869312067(-;AACA)
Make rs869312067(AACA;AACA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178539796
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312067
ebirs869312067
HLIrs869312067
Exacrs869312067
Varsomers869312067
Maprs869312067
PheGenIrs869312067
hapmaprs869312067
1000 genomesrs869312067
hgdprs869312067
ensemblrs869312067
gopubmedrs869312067
geneviewrs869312067
scholarrs869312067
googlers869312067
pharmgkbrs869312067
gwascentralrs869312067
openSNPrs869312067
23andMers869312067
23andMe allrs869312067
SNP Nexus

SNPshotrs869312067
SNPdbers869312067
MSV3drs869312067
GWAS Ctlgrs869312067
Max Magnitude0
ClinVar
Risk rs869312067(AACA;AACA)
Alt rs869312067(AACA;AACA)
Reference rs869312067(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179404524_179404527dupTGTT
CLNSRC
CLNACC RCV000209561.2,