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rs397517624

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517624(A;A)
Make rs397517624(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178599145
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517624
ebirs397517624
HLIrs397517624
Exacrs397517624
Varsomers397517624
Maprs397517624
PheGenIrs397517624
hapmaprs397517624
1000 genomesrs397517624
hgdprs397517624
ensemblrs397517624
gopubmedrs397517624
geneviewrs397517624
scholarrs397517624
googlers397517624
pharmgkbrs397517624
gwascentralrs397517624
openSNPrs397517624
23andMers397517624
23andMe allrs397517624
SNP Nexus

SNPshotrs397517624
SNPdbers397517624
MSV3drs397517624
GWAS Ctlgrs397517624
Max Magnitude0
ClinVar
Risk rs397517624(A;A)
Alt rs397517624(A;A)
Reference rs397517624(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.179463872C>T
CLNSRC ClinVar
CLNACC RCV000040383.2,