Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057518598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057518598(-;-)
Make rs1057518598(-;CT)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position120526811
GeneCUL4B
is asnp
is mentioned by
dbSNPrs1057518598
dbSNP (old)rs1057518598
ClinGenrs1057518598
ebirs1057518598
HLIrs1057518598
Exacrs1057518598
Gnomadrs1057518598
Varsomers1057518598
Maprs1057518598
PheGenIrs1057518598
Biobankrs1057518598
1000 genomesrs1057518598
hgdprs1057518598
ensemblrs1057518598
gopubmedrs1057518598
geneviewrs1057518598
scholarrs1057518598
googlers1057518598
pharmgkbrs1057518598
gwascentralrs1057518598
openSNPrs1057518598
23andMers1057518598
23andMe allrs1057518598
SNPshotrs1057518598
SNPdbers1057518598
MSV3drs1057518598
GWAS Ctlgrs1057518598
Max Magnitude0
ClinVar
Risk rs1057518598(-;-)
Alt rs1057518598(-;-)
Reference Rs1057518598(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUL4B
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119660666_119660667delAG
CLNSRC
CLNACC RCV000414203.1,