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rs869312041

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312041(-;-)
Make rs869312041(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178682904
GeneTTN
is asnp
is mentioned by
dbSNPrs869312041
ebirs869312041
HLIrs869312041
Exacrs869312041
Varsomers869312041
Maprs869312041
PheGenIrs869312041
hapmaprs869312041
1000 genomesrs869312041
hgdprs869312041
ensemblrs869312041
gopubmedrs869312041
geneviewrs869312041
scholarrs869312041
googlers869312041
pharmgkbrs869312041
gwascentralrs869312041
openSNPrs869312041
23andMers869312041
23andMe allrs869312041
SNP Nexus

SNPshotrs869312041
SNPdbers869312041
MSV3drs869312041
GWAS Ctlgrs869312041
Max Magnitude0
ClinVar
Risk rs869312041(;)
Alt rs869312041(;)
Reference rs869312041(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179547631delC
CLNSRC
CLNACC RCV000209671.1,