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rs1057518009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518009(G;T)
Make rs1057518009(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178584668
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1057518009
dbSNP (classic)rs1057518009
ClinGenrs1057518009
ebirs1057518009
HLIrs1057518009
Exacrs1057518009
Gnomadrs1057518009
Varsomers1057518009
LitVarrs1057518009
Maprs1057518009
PheGenIrs1057518009
Biobankrs1057518009
1000 genomesrs1057518009
hgdprs1057518009
ensemblrs1057518009
geneviewrs1057518009
scholarrs1057518009
googlers1057518009
pharmgkbrs1057518009
gwascentralrs1057518009
openSNPrs1057518009
23andMers1057518009
SNPshotrs1057518009
SNPdbers1057518009
MSV3drs1057518009
GWAS Ctlgrs1057518009
Max Magnitude0
ClinVar
Risk rs1057518009(T;T)
Alt rs1057518009(T;T)
Reference Rs1057518009(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179449395C>A
CLNSRC
CLNACC RCV000414745.1,