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rs397517695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517695(-;-)
Make rs397517695(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position178572305
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517695
ebirs397517695
HLIrs397517695
Exacrs397517695
Varsomers397517695
Maprs397517695
PheGenIrs397517695
hapmaprs397517695
1000 genomesrs397517695
hgdprs397517695
ensemblrs397517695
gopubmedrs397517695
geneviewrs397517695
scholarrs397517695
googlers397517695
pharmgkbrs397517695
gwascentralrs397517695
openSNPrs397517695
23andMers397517695
23andMe allrs397517695
SNP Nexus

SNPshotrs397517695
SNPdbers397517695
MSV3drs397517695
GWAS Ctlgrs397517695
Max Magnitude0
ClinVar
Risk rs397517695(;)
Alt rs397517695(;)
Reference rs397517695(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.179437032delT
CLNSRC ClinVar
CLNACC RCV000040593.2,