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rs869312037

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs869312037(-;-)
Make rs869312037(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178770484
GeneTTN
is asnp
is mentioned by
dbSNPrs869312037
ebirs869312037
HLIrs869312037
Exacrs869312037
Varsomers869312037
Maprs869312037
PheGenIrs869312037
hapmaprs869312037
1000 genomesrs869312037
hgdprs869312037
ensemblrs869312037
gopubmedrs869312037
geneviewrs869312037
scholarrs869312037
googlers869312037
pharmgkbrs869312037
gwascentralrs869312037
openSNPrs869312037
23andMers869312037
23andMe allrs869312037
SNP Nexus

SNPshotrs869312037
SNPdbers869312037
MSV3drs869312037
GWAS Ctlgrs869312037
Max Magnitude0
ClinVar
Risk rs869312037(;)
Alt rs869312037(;)
Reference rs869312037(TG;TG)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179635211_179635212delCA
CLNSRC
CLNACC RCV000209178.2,