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rs869312039

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312039(C;T)
Make rs869312039(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178740476
GeneTTN
is asnp
is mentioned by
dbSNPrs869312039
ebirs869312039
HLIrs869312039
Exacrs869312039
Varsomers869312039
Maprs869312039
PheGenIrs869312039
hapmaprs869312039
1000 genomesrs869312039
hgdprs869312039
ensemblrs869312039
gopubmedrs869312039
geneviewrs869312039
scholarrs869312039
googlers869312039
pharmgkbrs869312039
gwascentralrs869312039
openSNPrs869312039
23andMers869312039
23andMe allrs869312039
SNP Nexus

SNPshotrs869312039
SNPdbers869312039
MSV3drs869312039
GWAS Ctlgrs869312039
Max Magnitude0
ClinVar
Risk rs869312039(T;T)
Alt rs869312039(T;T)
Reference rs869312039(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179605203G>A
CLNSRC
CLNACC RCV000208993.1,