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rs1057519007

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs1057519007(-;-)
Make rs1057519007(-;CC)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41215906
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1057519007
dbSNP (old)rs1057519007
ClinGenrs1057519007
ebirs1057519007
HLIrs1057519007
Exacrs1057519007
Gnomadrs1057519007
Varsomers1057519007
Maprs1057519007
PheGenIrs1057519007
Biobankrs1057519007
1000 genomesrs1057519007
hgdprs1057519007
ensemblrs1057519007
gopubmedrs1057519007
geneviewrs1057519007
scholarrs1057519007
googlers1057519007
pharmgkbrs1057519007
gwascentralrs1057519007
openSNPrs1057519007
23andMers1057519007
23andMe allrs1057519007
SNPshotrs1057519007
SNPdbers1057519007
MSV3drs1057519007
GWAS Ctlgrs1057519007
Max Magnitude0
ClinVar
Risk rs1057519007(-;-)
Alt rs1057519007(-;-)
Reference Rs1057519007(CC;CC)
Significance Probable-Pathogenic
Disease Severe intellectual deficiency
Variation info
Gene USP9X
CLNDBN Severe intellectual deficiency
Reversed 0
HGVS NC_000023.10:g.41075159_41075160delCC
CLNSRC
CLNACC RCV000415029.1,