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rs1060500479

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060500479(-;-)
Make rs1060500479(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178581558
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1060500479
dbSNP (classic)rs1060500479
ClinGenrs1060500479
ebirs1060500479
HLIrs1060500479
Exacrs1060500479
Gnomadrs1060500479
Varsomers1060500479
LitVarrs1060500479
Maprs1060500479
PheGenIrs1060500479
Biobankrs1060500479
1000 genomesrs1060500479
hgdprs1060500479
ensemblrs1060500479
geneviewrs1060500479
scholarrs1060500479
googlers1060500479
pharmgkbrs1060500479
gwascentralrs1060500479
openSNPrs1060500479
23andMers1060500479
SNPshotrs1060500479
SNPdbers1060500479
MSV3drs1060500479
GWAS Ctlgrs1060500479
Max Magnitude0
ClinVar
Risk rs1060500479(-;-)
Alt rs1060500479(-;-)
Reference Rs1060500479(A;A)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179446285delT
CLNSRC
CLNACC RCV000467745.1,