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

rs869312057

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312057(G;T)
Make rs869312057(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178567948
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312057
ebirs869312057
HLIrs869312057
Exacrs869312057
Varsomers869312057
Maprs869312057
PheGenIrs869312057
hapmaprs869312057
1000 genomesrs869312057
hgdprs869312057
ensemblrs869312057
gopubmedrs869312057
geneviewrs869312057
scholarrs869312057
googlers869312057
pharmgkbrs869312057
gwascentralrs869312057
openSNPrs869312057
23andMers869312057
23andMe allrs869312057
SNP Nexus

SNPshotrs869312057
SNPdbers869312057
MSV3drs869312057
GWAS Ctlgrs869312057
Max Magnitude0
ClinVar
Risk rs869312057(T;T)
Alt rs869312057(T;T)
Reference rs869312057(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179432675C>A
CLNSRC
CLNACC RCV000209657.1,