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rs869312082

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312082(-;-)
Make rs869312082(-;T)
Make rs869312082(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178552577
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312082
ebirs869312082
HLIrs869312082
Exacrs869312082
Varsomers869312082
Maprs869312082
PheGenIrs869312082
hapmaprs869312082
1000 genomesrs869312082
hgdprs869312082
ensemblrs869312082
gopubmedrs869312082
geneviewrs869312082
scholarrs869312082
googlers869312082
pharmgkbrs869312082
gwascentralrs869312082
openSNPrs869312082
23andMers869312082
23andMe allrs869312082
SNP Nexus

SNPshotrs869312082
SNPdbers869312082
MSV3drs869312082
GWAS Ctlgrs869312082
Max Magnitude0
ClinVar
Risk rs869312082(T;T)
Alt rs869312082(T;T)
Reference rs869312082(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179417304_179417305insA
CLNSRC
CLNACC RCV000209276.1,