Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312086

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312086(A;A)
Make rs869312086(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178536302
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312086
ebirs869312086
HLIrs869312086
Exacrs869312086
Varsomers869312086
Maprs869312086
PheGenIrs869312086
hapmaprs869312086
1000 genomesrs869312086
hgdprs869312086
ensemblrs869312086
gopubmedrs869312086
geneviewrs869312086
scholarrs869312086
googlers869312086
pharmgkbrs869312086
gwascentralrs869312086
openSNPrs869312086
23andMers869312086
23andMe allrs869312086
SNP Nexus

SNPshotrs869312086
SNPdbers869312086
MSV3drs869312086
GWAS Ctlgrs869312086
Max Magnitude0
ClinVar
Risk rs869312086(A;A)
Alt rs869312086(A;A)
Reference rs869312086(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.179401029G>T
CLNSRC
CLNACC RCV000209762.1,