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rs397517633

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517633(-;-)
Make rs397517633(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position178594499
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517633
ebirs397517633
HLIrs397517633
Exacrs397517633
Varsomers397517633
Maprs397517633
PheGenIrs397517633
hapmaprs397517633
1000 genomesrs397517633
hgdprs397517633
ensemblrs397517633
gopubmedrs397517633
geneviewrs397517633
scholarrs397517633
googlers397517633
pharmgkbrs397517633
gwascentralrs397517633
openSNPrs397517633
23andMers397517633
23andMe allrs397517633
SNP Nexus

SNPshotrs397517633
SNPdbers397517633
MSV3drs397517633
GWAS Ctlgrs397517633
Max Magnitude0
ClinVar
Risk rs397517633(;)
Alt rs397517633(;)
Reference rs397517633(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179459226delT
CLNSRC ClinVar
CLNACC RCV000040401.2,