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rs869312045

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312045(-;-)
Make rs869312045(-;A)
Make rs869312045(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178620853
GeneTTN
is asnp
is mentioned by
dbSNPrs869312045
ebirs869312045
HLIrs869312045
Exacrs869312045
Varsomers869312045
Maprs869312045
PheGenIrs869312045
hapmaprs869312045
1000 genomesrs869312045
hgdprs869312045
ensemblrs869312045
gopubmedrs869312045
geneviewrs869312045
scholarrs869312045
googlers869312045
pharmgkbrs869312045
gwascentralrs869312045
openSNPrs869312045
23andMers869312045
23andMe allrs869312045
SNP Nexus

SNPshotrs869312045
SNPdbers869312045
MSV3drs869312045
GWAS Ctlgrs869312045
Max Magnitude0
ClinVar
Risk rs869312045(A;A)
Alt rs869312045(A;A)
Reference rs869312045(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179485581dupT
CLNSRC
CLNACC RCV000210254.1,