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rs397517587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517587(A;A)
Make rs397517587(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position178618768
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517587
ebirs397517587
HLIrs397517587
Exacrs397517587
Varsomers397517587
Maprs397517587
PheGenIrs397517587
hapmaprs397517587
1000 genomesrs397517587
hgdprs397517587
ensemblrs397517587
gopubmedrs397517587
geneviewrs397517587
scholarrs397517587
googlers397517587
pharmgkbrs397517587
gwascentralrs397517587
openSNPrs397517587
23andMers397517587
23andMe allrs397517587
SNP Nexus

SNPshotrs397517587
SNPdbers397517587
MSV3drs397517587
GWAS Ctlgrs397517587
Max Magnitude0
ClinVar
Risk rs397517587(A,T;A,T)
Alt rs397517587(A,T;A,T)
Reference rs397517587(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.179483495G>T
CLNSRC ClinVar
CLNACC RCV000209642.2,