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rs869312072

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312072(-;-)
Make rs869312072(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178594221
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312072
ebirs869312072
HLIrs869312072
Exacrs869312072
Varsomers869312072
Maprs869312072
PheGenIrs869312072
hapmaprs869312072
1000 genomesrs869312072
hgdprs869312072
ensemblrs869312072
gopubmedrs869312072
geneviewrs869312072
scholarrs869312072
googlers869312072
pharmgkbrs869312072
gwascentralrs869312072
openSNPrs869312072
23andMers869312072
23andMe allrs869312072
SNP Nexus

SNPshotrs869312072
SNPdbers869312072
MSV3drs869312072
GWAS Ctlgrs869312072
Max Magnitude0
ClinVar
Risk rs869312072(;)
Alt rs869312072(;)
Reference rs869312072(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.179458948delT
CLNSRC
CLNACC RCV000209042.1,