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

rs397517776

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs397517776(-;-)
Make rs397517776(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178539765
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs397517776
ebirs397517776
HLIrs397517776
Exacrs397517776
Varsomers397517776
Maprs397517776
PheGenIrs397517776
hapmaprs397517776
1000 genomesrs397517776
hgdprs397517776
ensemblrs397517776
gopubmedrs397517776
geneviewrs397517776
scholarrs397517776
googlers397517776
pharmgkbrs397517776
gwascentralrs397517776
openSNPrs397517776
23andMers397517776
23andMe allrs397517776
SNP Nexus

SNPshotrs397517776
SNPdbers397517776
MSV3drs397517776
GWAS Ctlgrs397517776
Max Magnitude0
ClinVar
Risk rs397517776(;)
Alt rs397517776(;)
Reference rs397517776(AG;AG)
Significance Probable-Pathogenic
Disease not specified Primary dilated cardiomyopathy Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN not specified Primary dilated cardiomyopathy Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179404492_179404493delCT
CLNSRC
CLNACC RCV000040868.2, RCV000209003.1, RCV000231491.1,