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rs397517830

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517830(G;T)
Make rs397517830(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position178741025
GeneTTN
is asnp
is mentioned by
dbSNPrs397517830
ebirs397517830
HLIrs397517830
Exacrs397517830
Varsomers397517830
Maprs397517830
PheGenIrs397517830
hapmaprs397517830
1000 genomesrs397517830
hgdprs397517830
ensemblrs397517830
gopubmedrs397517830
geneviewrs397517830
scholarrs397517830
googlers397517830
pharmgkbrs397517830
gwascentralrs397517830
openSNPrs397517830
23andMers397517830
23andMe allrs397517830
SNP Nexus

SNPshotrs397517830
SNPdbers397517830
MSV3drs397517830
GWAS Ctlgrs397517830
Max Magnitude0
ClinVar
Risk rs397517830(A;A)
Alt rs397517830(A;A)
Reference rs397517830(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179605752C>A
CLNSRC ClinVar
CLNACC RCV000041089.2,