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rs397517628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517628(-;-)
Make rs397517628(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178597955
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517628
ebirs397517628
HLIrs397517628
Exacrs397517628
Varsomers397517628
Maprs397517628
PheGenIrs397517628
hapmaprs397517628
1000 genomesrs397517628
hgdprs397517628
ensemblrs397517628
gopubmedrs397517628
geneviewrs397517628
scholarrs397517628
googlers397517628
pharmgkbrs397517628
gwascentralrs397517628
openSNPrs397517628
23andMers397517628
23andMe allrs397517628
SNP Nexus

SNPshotrs397517628
SNPdbers397517628
MSV3drs397517628
GWAS Ctlgrs397517628
Max Magnitude0
ClinVar
Risk rs397517628(;)
Alt rs397517628(;)
Reference rs397517628(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.179462682delC
CLNSRC ClinVar
CLNACC RCV000040389.2,