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rs397517698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs397517698(-;-)
Make rs397517698(-;AAAG)
ReferenceGRCh38 38.1/141
Chromosome2
Position178775030
GeneTTN
is asnp
is mentioned by
dbSNPrs397517698
ebirs397517698
HLIrs397517698
Exacrs397517698
Varsomers397517698
Maprs397517698
PheGenIrs397517698
hapmaprs397517698
1000 genomesrs397517698
hgdprs397517698
ensemblrs397517698
gopubmedrs397517698
geneviewrs397517698
scholarrs397517698
googlers397517698
pharmgkbrs397517698
gwascentralrs397517698
openSNPrs397517698
23andMers397517698
23andMe allrs397517698
SNP Nexus

SNPshotrs397517698
SNPdbers397517698
MSV3drs397517698
GWAS Ctlgrs397517698
Max Magnitude0
ClinVar
Risk rs397517698(;)
Alt rs397517698(;)
Reference rs397517698(AAAG;AAAG)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN LOC101927055
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179639757_179639760delCTTT
CLNSRC ClinVar
CLNACC RCV000040597.2,