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rs1057518039

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518039(A;G)
Make rs1057518039(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position120560217
GeneCUL4B
is asnp
is mentioned by
dbSNPrs1057518039
dbSNP (classic)rs1057518039
ClinGenrs1057518039
ebirs1057518039
HLIrs1057518039
Exacrs1057518039
Gnomadrs1057518039
Varsomers1057518039
LitVarrs1057518039
Maprs1057518039
PheGenIrs1057518039
Biobankrs1057518039
1000 genomesrs1057518039
hgdprs1057518039
ensemblrs1057518039
geneviewrs1057518039
scholarrs1057518039
googlers1057518039
pharmgkbrs1057518039
gwascentralrs1057518039
openSNPrs1057518039
23andMers1057518039
23andMe allrs1057518039
SNPshotrs1057518039
SNPdbers1057518039
MSV3drs1057518039
GWAS Ctlgrs1057518039
Max Magnitude0
ClinVar
Risk rs1057518039(G;G)
Alt rs1057518039(G;G)
Reference Rs1057518039(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUL4B
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119694072T>C
CLNSRC
CLNACC RCV000414616.1,