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rs1057524248

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524248(C;T)
Make rs1057524248(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41137011
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1057524248
dbSNP (classic)rs1057524248
ClinGenrs1057524248
ebirs1057524248
HLIrs1057524248
Exacrs1057524248
Gnomadrs1057524248
Varsomers1057524248
LitVarrs1057524248
Maprs1057524248
PheGenIrs1057524248
Biobankrs1057524248
1000 genomesrs1057524248
hgdprs1057524248
ensemblrs1057524248
geneviewrs1057524248
scholarrs1057524248
googlers1057524248
pharmgkbrs1057524248
gwascentralrs1057524248
openSNPrs1057524248
23andMers1057524248
23andMe allrs1057524248
SNPshotrs1057524248
SNPdbers1057524248
MSV3drs1057524248
GWAS Ctlgrs1057524248
Max Magnitude0
ClinVar
Risk rs1057524248(T;T)
Alt rs1057524248(T;T)
Reference Rs1057524248(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.40996264C>T
CLNSRC
CLNACC RCV000431532.1,