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rs869312112

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312112(C;T)
Make rs869312112(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178590230
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312112
ebirs869312112
HLIrs869312112
Exacrs869312112
Varsomers869312112
Maprs869312112
PheGenIrs869312112
hapmaprs869312112
1000 genomesrs869312112
hgdprs869312112
ensemblrs869312112
gopubmedrs869312112
geneviewrs869312112
scholarrs869312112
googlers869312112
pharmgkbrs869312112
gwascentralrs869312112
openSNPrs869312112
23andMers869312112
23andMe allrs869312112
SNP Nexus

SNPshotrs869312112
SNPdbers869312112
MSV3drs869312112
GWAS Ctlgrs869312112
Max Magnitude0
ClinVar
Risk rs869312112(T;T)
Alt rs869312112(T;T)
Reference rs869312112(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.179454957G>A
CLNSRC
CLNACC RCV000209451.1,