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rs869312076

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312076(-;-)
Make rs869312076(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178575341
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312076
ebirs869312076
HLIrs869312076
Exacrs869312076
Varsomers869312076
Maprs869312076
PheGenIrs869312076
hapmaprs869312076
1000 genomesrs869312076
hgdprs869312076
ensemblrs869312076
gopubmedrs869312076
geneviewrs869312076
scholarrs869312076
googlers869312076
pharmgkbrs869312076
gwascentralrs869312076
openSNPrs869312076
23andMers869312076
23andMe allrs869312076
SNP Nexus

SNPshotrs869312076
SNPdbers869312076
MSV3drs869312076
GWAS Ctlgrs869312076
Max Magnitude0
ClinVar
Risk rs869312076(;)
Alt rs869312076(;)
Reference rs869312076(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179440068delT
CLNSRC
CLNACC RCV000209524.1,