Have questions? Visit https://www.reddit.com/r/SNPedia

rs397517626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517626(-;-)
Make rs397517626(-;A)
Make rs397517626(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position178598977
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517626
ebirs397517626
HLIrs397517626
Exacrs397517626
Varsomers397517626
Maprs397517626
PheGenIrs397517626
hapmaprs397517626
1000 genomesrs397517626
hgdprs397517626
ensemblrs397517626
gopubmedrs397517626
geneviewrs397517626
scholarrs397517626
googlers397517626
pharmgkbrs397517626
gwascentralrs397517626
openSNPrs397517626
23andMers397517626
23andMe allrs397517626
SNP Nexus

SNPshotrs397517626
SNPdbers397517626
MSV3drs397517626
GWAS Ctlgrs397517626
Max Magnitude0
ClinVar
Risk rs397517626(A;A)
Alt rs397517626(A;A)
Reference rs397517626(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179463705dupT
CLNSRC ClinVar
CLNACC RCV000040385.2,