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rs1057518476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs1057518476(-;-)
Make rs1057518476(-;TT)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71291854
GeneNONO
is asnp
is mentioned by
dbSNPrs1057518476
dbSNP (classic)rs1057518476
ClinGenrs1057518476
ebirs1057518476
HLIrs1057518476
Exacrs1057518476
Gnomadrs1057518476
Varsomers1057518476
LitVarrs1057518476
Maprs1057518476
PheGenIrs1057518476
Biobankrs1057518476
1000 genomesrs1057518476
hgdprs1057518476
ensemblrs1057518476
geneviewrs1057518476
scholarrs1057518476
googlers1057518476
pharmgkbrs1057518476
gwascentralrs1057518476
openSNPrs1057518476
23andMers1057518476
23andMe allrs1057518476
SNPshotrs1057518476
SNPdbers1057518476
MSV3drs1057518476
GWAS Ctlgrs1057518476
Max Magnitude0
ClinVar
Risk rs1057518476(-;-)
Alt rs1057518476(-;-)
Reference Rs1057518476(TT;TT)
Significance Pathogenic
Disease not provided
Variation info
Gene NONO
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70511704_70511705delTT
CLNSRC
CLNACC RCV000413763.1,