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rs397517664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517664(A;A)
Make rs397517664(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position178581650
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517664
ebirs397517664
HLIrs397517664
Exacrs397517664
Varsomers397517664
Maprs397517664
PheGenIrs397517664
hapmaprs397517664
1000 genomesrs397517664
hgdprs397517664
ensemblrs397517664
gopubmedrs397517664
geneviewrs397517664
scholarrs397517664
googlers397517664
pharmgkbrs397517664
gwascentralrs397517664
openSNPrs397517664
23andMers397517664
23andMe allrs397517664
SNP Nexus

SNPshotrs397517664
SNPdbers397517664
MSV3drs397517664
GWAS Ctlgrs397517664
Max Magnitude0
ClinVar
Risk rs397517664(A;A)
Alt rs397517664(A;A)
Reference rs397517664(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179446377G>T
CLNSRC ClinVar
CLNACC RCV000040507.2,