rs1057518598

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CT;CT)	0	common in clinvar

Make rs1057518598(-;-)

Make rs1057518598(-;CT)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

120526811

Gene

CUL4B

is a	snp
is	mentioned by
dbSNP	rs1057518598
dbSNP (classic)	rs1057518598
ClinGen	rs1057518598
ebi	rs1057518598
HLI	rs1057518598
Exac	rs1057518598
Gnomad	rs1057518598
Varsome	rs1057518598
LitVar	rs1057518598
Map	rs1057518598
PheGenI	rs1057518598
Biobank	rs1057518598
1000 genomes	rs1057518598
hgdp	rs1057518598
ensembl	rs1057518598
geneview	rs1057518598
scholar	rs1057518598
google	rs1057518598
pharmgkb	rs1057518598
gwascentral	rs1057518598
openSNP	rs1057518598
23andMe	rs1057518598
SNPshot	rs1057518598
SNPdbe	rs1057518598
MSV3d	rs1057518598
GWAS Ctlg	rs1057518598

Max Magnitude

0

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,