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rs869312119

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312119(C;T)
Make rs869312119(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178561756
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312119
ebirs869312119
HLIrs869312119
Exacrs869312119
Varsomers869312119
Maprs869312119
PheGenIrs869312119
hapmaprs869312119
1000 genomesrs869312119
hgdprs869312119
ensemblrs869312119
gopubmedrs869312119
geneviewrs869312119
scholarrs869312119
googlers869312119
pharmgkbrs869312119
gwascentralrs869312119
openSNPrs869312119
23andMers869312119
23andMe allrs869312119
SNP Nexus

SNPshotrs869312119
SNPdbers869312119
MSV3drs869312119
GWAS Ctlgrs869312119
Max Magnitude0
ClinVar
Risk rs869312119(T;T)
Alt rs869312119(T;T)
Reference rs869312119(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179426483G>A
CLNSRC
CLNACC RCV000209333.1,