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rs1060500556

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500556(-;-)
Make rs1060500556(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178561650
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1060500556
dbSNP (classic)rs1060500556
ClinGenrs1060500556
ebirs1060500556
HLIrs1060500556
Exacrs1060500556
Gnomadrs1060500556
Varsomers1060500556
LitVarrs1060500556
Maprs1060500556
PheGenIrs1060500556
Biobankrs1060500556
1000 genomesrs1060500556
hgdprs1060500556
ensemblrs1060500556
geneviewrs1060500556
scholarrs1060500556
googlers1060500556
pharmgkbrs1060500556
gwascentralrs1060500556
openSNPrs1060500556
23andMers1060500556
SNPshotrs1060500556
SNPdbers1060500556
MSV3drs1060500556
GWAS Ctlgrs1060500556
Max Magnitude0
ClinVar
Risk rs1060500556(-;-)
Alt rs1060500556(-;-)
Reference Rs1060500556(C;C)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179426377delG
CLNSRC
CLNACC RCV000467174.1,