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rs869312064

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs869312064(-;-)
Make rs869312064(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178552812
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312064
ebirs869312064
HLIrs869312064
Exacrs869312064
Varsomers869312064
Maprs869312064
PheGenIrs869312064
hapmaprs869312064
1000 genomesrs869312064
hgdprs869312064
ensemblrs869312064
gopubmedrs869312064
geneviewrs869312064
scholarrs869312064
googlers869312064
pharmgkbrs869312064
gwascentralrs869312064
openSNPrs869312064
23andMers869312064
23andMe allrs869312064
SNP Nexus

SNPshotrs869312064
SNPdbers869312064
MSV3drs869312064
GWAS Ctlgrs869312064
Max Magnitude0
ClinVar
Risk rs869312064(;)
Alt rs869312064(;)
Reference rs869312064(AG;AG)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179417539_179417540delCT
CLNSRC
CLNACC RCV000209211.1,