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rs397517643

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517643(-;-)
Make rs397517643(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178592914
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517643
ebirs397517643
HLIrs397517643
Exacrs397517643
Varsomers397517643
Maprs397517643
PheGenIrs397517643
hapmaprs397517643
1000 genomesrs397517643
hgdprs397517643
ensemblrs397517643
gopubmedrs397517643
geneviewrs397517643
scholarrs397517643
googlers397517643
pharmgkbrs397517643
gwascentralrs397517643
openSNPrs397517643
23andMers397517643
23andMe allrs397517643
SNP Nexus

SNPshotrs397517643
SNPdbers397517643
MSV3drs397517643
GWAS Ctlgrs397517643
Max Magnitude0
ClinVar
Risk rs397517643(;)
Alt rs397517643(;)
Reference rs397517643(G;G)
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.179457641delC
CLNSRC ClinVar
CLNACC RCV000040417.2, RCV000184316.1,