Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312059

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGATGCT;CAGATGCT) 0 common in clinvar
Make rs869312059(-;-)
Make rs869312059(-;CAGATGCT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178564863
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312059
ClinGenrs869312059
ebirs869312059
HLIrs869312059
Exacrs869312059
Varsomers869312059
Maprs869312059
PheGenIrs869312059
hapmaprs869312059
1000 genomesrs869312059
hgdprs869312059
ensemblrs869312059
gopubmedrs869312059
geneviewrs869312059
scholarrs869312059
googlers869312059
pharmgkbrs869312059
gwascentralrs869312059
openSNPrs869312059
23andMers869312059
23andMe allrs869312059
SNP Nexus

SNPshotrs869312059
SNPdbers869312059
MSV3drs869312059
GWAS Ctlgrs869312059
Max Magnitude0
ClinVar
Risk rs869312059(-;-)
Alt rs869312059(-;-)
Reference Rs869312059(CAGATGCT;CAGATGCT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179429590_179429597delAGCATCTG
CLNSRC
CLNACC RCV000209362.1,