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rs397517631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517631(A;A)
Make rs397517631(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178595506
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517631
ebirs397517631
HLIrs397517631
Exacrs397517631
Varsomers397517631
Maprs397517631
PheGenIrs397517631
hapmaprs397517631
1000 genomesrs397517631
hgdprs397517631
ensemblrs397517631
gopubmedrs397517631
geneviewrs397517631
scholarrs397517631
googlers397517631
pharmgkbrs397517631
gwascentralrs397517631
openSNPrs397517631
23andMers397517631
23andMe allrs397517631
SNP Nexus

SNPshotrs397517631
SNPdbers397517631
MSV3drs397517631
GWAS Ctlgrs397517631
Max Magnitude0
ClinVar
Risk rs397517631(A,C;A,C)
Alt rs397517631(A,C;A,C)
Reference rs397517631(G;G)
Significance Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179460233C>G; NC_000002.11:g.179460233C>T
CLNSRC ClinVar
CLNACC RCV000184243.1, RCV000040399.2,