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

rs1060500586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500586(G;T)
Make rs1060500586(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178557795
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1060500586
dbSNP (classic)rs1060500586
ClinGenrs1060500586
ebirs1060500586
HLIrs1060500586
Exacrs1060500586
Gnomadrs1060500586
Varsomers1060500586
LitVarrs1060500586
Maprs1060500586
PheGenIrs1060500586
Biobankrs1060500586
1000 genomesrs1060500586
hgdprs1060500586
ensemblrs1060500586
geneviewrs1060500586
scholarrs1060500586
googlers1060500586
pharmgkbrs1060500586
gwascentralrs1060500586
openSNPrs1060500586
23andMers1060500586
SNPshotrs1060500586
SNPdbers1060500586
MSV3drs1060500586
GWAS Ctlgrs1060500586
Max Magnitude0
ClinVar
Risk rs1060500586(T;T)
Alt rs1060500586(T;T)
Reference Rs1060500586(G;G)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179422522C>A
CLNSRC
CLNACC RCV000467875.1,