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

rs397517758

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517758(-;-)
Make rs397517758(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178547729
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517758
ebirs397517758
HLIrs397517758
Exacrs397517758
Varsomers397517758
Maprs397517758
PheGenIrs397517758
hapmaprs397517758
1000 genomesrs397517758
hgdprs397517758
ensemblrs397517758
gopubmedrs397517758
geneviewrs397517758
scholarrs397517758
googlers397517758
pharmgkbrs397517758
gwascentralrs397517758
openSNPrs397517758
23andMers397517758
23andMe allrs397517758
SNP Nexus

SNPshotrs397517758
SNPdbers397517758
MSV3drs397517758
GWAS Ctlgrs397517758
Max Magnitude0
ClinVar
Risk rs397517758(;)
Alt rs397517758(;)
Reference rs397517758(T;T)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000002.11:g.179412456delA
CLNSRC ClinVar
CLNACC RCV000040804.3, RCV000184359.1,