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rs1057518114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs1057518114(-;-)
Make rs1057518114(-;CTT)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41136888
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1057518114
dbSNP (classic)rs1057518114
ClinGenrs1057518114
ebirs1057518114
HLIrs1057518114
Exacrs1057518114
Gnomadrs1057518114
Varsomers1057518114
LitVarrs1057518114
Maprs1057518114
PheGenIrs1057518114
Biobankrs1057518114
1000 genomesrs1057518114
hgdprs1057518114
ensemblrs1057518114
geneviewrs1057518114
scholarrs1057518114
googlers1057518114
pharmgkbrs1057518114
gwascentralrs1057518114
openSNPrs1057518114
23andMers1057518114
23andMe allrs1057518114
SNPshotrs1057518114
SNPdbers1057518114
MSV3drs1057518114
GWAS Ctlgrs1057518114
Max Magnitude0
ClinVar
Risk rs1057518114(-;-)
Alt rs1057518114(-;-)
Reference Rs1057518114(CTT;CTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.40996141_40996143delCTT
CLNSRC
CLNACC RCV000413770.1,