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rs397517741

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGT;GGT) 0 common in clinvar
Make rs397517741(-;-)
Make rs397517741(-;GGT)
ReferenceGRCh38 38.1/141
Chromosome2
Position178553912
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517741
ebirs397517741
HLIrs397517741
Exacrs397517741
Varsomers397517741
Maprs397517741
PheGenIrs397517741
hapmaprs397517741
1000 genomesrs397517741
hgdprs397517741
ensemblrs397517741
gopubmedrs397517741
geneviewrs397517741
scholarrs397517741
googlers397517741
pharmgkbrs397517741
gwascentralrs397517741
openSNPrs397517741
23andMers397517741
23andMe allrs397517741
SNP Nexus

SNPshotrs397517741
SNPdbers397517741
MSV3drs397517741
GWAS Ctlgrs397517741
Max Magnitude0
ClinVar
Risk rs397517741(;)
Alt rs397517741(;)
Reference rs397517741(GGT;GGT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179418639_179418641delACC
CLNSRC ClinVar
CLNACC RCV000040755.2,