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rs869312078

From SNPedia

Orientationminus
Geno Mag Summary
(TAAT;TAAT) 0 common in clinvar
Make rs869312078(-;-)
Make rs869312078(-;TAAT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178569746
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312078
ebirs869312078
HLIrs869312078
Exacrs869312078
Varsomers869312078
Maprs869312078
PheGenIrs869312078
hapmaprs869312078
1000 genomesrs869312078
hgdprs869312078
ensemblrs869312078
gopubmedrs869312078
geneviewrs869312078
scholarrs869312078
googlers869312078
pharmgkbrs869312078
gwascentralrs869312078
openSNPrs869312078
23andMers869312078
23andMe allrs869312078
SNP Nexus

SNPshotrs869312078
SNPdbers869312078
MSV3drs869312078
GWAS Ctlgrs869312078
Max Magnitude0
ClinVar
Risk rs869312078(;)
Alt rs869312078(;)
Reference rs869312078(TAAT;TAAT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179434473_179434476delATTA
CLNSRC
CLNACC RCV000209545.1,