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

rs869312065

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312065(C;T)
Make rs869312065(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178548943
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312065
ebirs869312065
HLIrs869312065
Exacrs869312065
Varsomers869312065
Maprs869312065
PheGenIrs869312065
hapmaprs869312065
1000 genomesrs869312065
hgdprs869312065
ensemblrs869312065
gopubmedrs869312065
geneviewrs869312065
scholarrs869312065
googlers869312065
pharmgkbrs869312065
gwascentralrs869312065
openSNPrs869312065
23andMers869312065
23andMe allrs869312065
SNP Nexus

SNPshotrs869312065
SNPdbers869312065
MSV3drs869312065
GWAS Ctlgrs869312065
Max Magnitude0
ClinVar
Risk rs869312065(T;T)
Alt rs869312065(T;T)
Reference rs869312065(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.179413670G>A
CLNSRC
CLNACC RCV000209537.1,