rs1060499753

Orientation

minus

Stabilized

minus

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

Make rs1060499753(-;-)

Make rs1060499753(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

83683022

Gene

UBQLN1

is a	snp
is	mentioned by
dbSNP	rs1060499753
dbSNP (classic)	rs1060499753
ClinGen	rs1060499753
ebi	rs1060499753
HLI	rs1060499753
Exac	rs1060499753
Gnomad	rs1060499753
Varsome	rs1060499753
LitVar	rs1060499753
Map	rs1060499753
PheGenI	rs1060499753
Biobank	rs1060499753
1000 genomes	rs1060499753
hgdp	rs1060499753
ensembl	rs1060499753
geneview	rs1060499753
scholar	rs1060499753
google	rs1060499753
pharmgkb	rs1060499753
gwascentral	rs1060499753
openSNP	rs1060499753
23andMe	rs1060499753
SNPshot	rs1060499753
SNPdbe	rs1060499753
MSV3d	rs1060499753
GWAS Ctlg	rs1060499753

Max Magnitude

0

ClinVar
Risk	rs1060499753(-;-)
Alt	rs1060499753(-;-)
Reference	Rs1060499753(A;A)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	UBQLN1
CLNDBN	Abnormality of brain morphology
Reversed	1
HGVS	NC_000009.11:g.86297937delT
CLNSRC
CLNACC	RCV000454188.1,