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rs869312080

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs869312080(-;-)
Make rs869312080(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178559672
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312080
ebirs869312080
HLIrs869312080
Exacrs869312080
Varsomers869312080
Maprs869312080
PheGenIrs869312080
hapmaprs869312080
1000 genomesrs869312080
hgdprs869312080
ensemblrs869312080
gopubmedrs869312080
geneviewrs869312080
scholarrs869312080
googlers869312080
pharmgkbrs869312080
gwascentralrs869312080
openSNPrs869312080
23andMers869312080
23andMe allrs869312080
SNP Nexus

SNPshotrs869312080
SNPdbers869312080
MSV3drs869312080
GWAS Ctlgrs869312080
Max Magnitude0
ClinVar
Risk rs869312080(;)
Alt rs869312080(;)
Reference rs869312080(CT;CT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179424399_179424400delAG
CLNSRC
CLNACC RCV000209254.1,