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rs397517721

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517721(G;T)
Make rs397517721(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178564600
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517721
ebirs397517721
HLIrs397517721
Exacrs397517721
Varsomers397517721
Maprs397517721
PheGenIrs397517721
hapmaprs397517721
1000 genomesrs397517721
hgdprs397517721
ensemblrs397517721
gopubmedrs397517721
geneviewrs397517721
scholarrs397517721
googlers397517721
pharmgkbrs397517721
gwascentralrs397517721
openSNPrs397517721
23andMers397517721
23andMe allrs397517721
SNP Nexus

SNPshotrs397517721
SNPdbers397517721
MSV3drs397517721
GWAS Ctlgrs397517721
Max Magnitude0
ClinVar
Risk rs397517721(T;T)
Alt rs397517721(T;T)
Reference rs397517721(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.179429327C>A
CLNSRC ClinVar
CLNACC RCV000040667.2,