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rs1057518174

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518174(A;A)
Make rs1057518174(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position41170234
GeneUSP9X
is asnp
is mentioned by
dbSNPrs1057518174
dbSNP (old)rs1057518174
ClinGenrs1057518174
ebirs1057518174
HLIrs1057518174
Exacrs1057518174
Gnomadrs1057518174
Varsomers1057518174
Maprs1057518174
PheGenIrs1057518174
Biobankrs1057518174
1000 genomesrs1057518174
hgdprs1057518174
ensemblrs1057518174
gopubmedrs1057518174
geneviewrs1057518174
scholarrs1057518174
googlers1057518174
pharmgkbrs1057518174
gwascentralrs1057518174
openSNPrs1057518174
23andMers1057518174
23andMe allrs1057518174
SNPshotrs1057518174
SNPdbers1057518174
MSV3drs1057518174
GWAS Ctlgrs1057518174
Max Magnitude0
ClinVar
Risk rs1057518174(A;A)
Alt rs1057518174(A;A)
Reference Rs1057518174(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene USP9X
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.41029487C>A
CLNSRC
CLNACC RCV000413876.1,