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rs397517749

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517749(-;-)
Make rs397517749(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position178552313
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517749
ebirs397517749
HLIrs397517749
Exacrs397517749
Varsomers397517749
Maprs397517749
PheGenIrs397517749
hapmaprs397517749
1000 genomesrs397517749
hgdprs397517749
ensemblrs397517749
gopubmedrs397517749
geneviewrs397517749
scholarrs397517749
googlers397517749
pharmgkbrs397517749
gwascentralrs397517749
openSNPrs397517749
23andMers397517749
23andMe allrs397517749
SNP Nexus

SNPshotrs397517749
SNPdbers397517749
MSV3drs397517749
GWAS Ctlgrs397517749
Max Magnitude0
ClinVar
Risk rs397517749(;)
Alt rs397517749(;)
Reference rs397517749(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179417040delT
CLNSRC ClinVar
CLNACC RCV000040767.2,