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rs869312122

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869312122(-;-)
Make rs869312122(-;T)
Make rs869312122(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178535516
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312122
ebirs869312122
HLIrs869312122
Exacrs869312122
Varsomers869312122
Maprs869312122
PheGenIrs869312122
hapmaprs869312122
1000 genomesrs869312122
hgdprs869312122
ensemblrs869312122
gopubmedrs869312122
geneviewrs869312122
scholarrs869312122
googlers869312122
pharmgkbrs869312122
gwascentralrs869312122
openSNPrs869312122
23andMers869312122
23andMe allrs869312122
SNP Nexus

SNPshotrs869312122
SNPdbers869312122
MSV3drs869312122
GWAS Ctlgrs869312122
Max Magnitude0
ClinVar
Risk rs869312122(T;T)
Alt rs869312122(T;T)
Reference rs869312122(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179400243_179400244insA
CLNSRC
CLNACC RCV000209694.1,