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

rs1057518003

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518003(C;T)
Make rs1057518003(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178531962
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs1057518003
dbSNP (old)rs1057518003
ClinGenrs1057518003
ebirs1057518003
HLIrs1057518003
Exacrs1057518003
Gnomadrs1057518003
Varsomers1057518003
Maprs1057518003
PheGenIrs1057518003
Biobankrs1057518003
1000 genomesrs1057518003
hgdprs1057518003
ensemblrs1057518003
gopubmedrs1057518003
geneviewrs1057518003
scholarrs1057518003
googlers1057518003
pharmgkbrs1057518003
gwascentralrs1057518003
openSNPrs1057518003
23andMers1057518003
23andMe allrs1057518003
SNPshotrs1057518003
SNPdbers1057518003
MSV3drs1057518003
GWAS Ctlgrs1057518003
Max Magnitude0
ClinVar
Risk rs1057518003(T;T)
Alt rs1057518003(T;T)
Reference Rs1057518003(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179396689G>A
CLNSRC
CLNACC RCV000412765.1,