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

rs397517735

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517735(A;A)
Make rs397517735(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178559309
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517735
ebirs397517735
HLIrs397517735
Exacrs397517735
Varsomers397517735
Maprs397517735
PheGenIrs397517735
hapmaprs397517735
1000 genomesrs397517735
hgdprs397517735
ensemblrs397517735
gopubmedrs397517735
geneviewrs397517735
scholarrs397517735
googlers397517735
pharmgkbrs397517735
gwascentralrs397517735
openSNPrs397517735
23andMers397517735
23andMe allrs397517735
SNP Nexus

SNPshotrs397517735
SNPdbers397517735
MSV3drs397517735
GWAS Ctlgrs397517735
Max Magnitude0
ClinVar
Risk rs397517735(A;A)
Alt rs397517735(A;A)
Reference rs397517735(T;T)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy not provided Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179424036A>T
CLNSRC ClinVar
CLNACC RCV000040727.2, RCV000184278.2, RCV000234171.1,