rs864309702

Orientation

minus

Stabilized

minus

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

Make rs864309702(-;-)

Make rs864309702(-;TTAG)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

40074207

Gene

BCOR

is a	snp
is	mentioned by
dbSNP	rs864309702
dbSNP (classic)	rs864309702
ClinGen	rs864309702
ebi	rs864309702
HLI	rs864309702
Exac	rs864309702
Gnomad	rs864309702
Varsome	rs864309702
LitVar	rs864309702
Map	rs864309702
PheGenI	rs864309702
Biobank	rs864309702
1000 genomes	rs864309702
hgdp	rs864309702
ensembl	rs864309702
geneview	rs864309702
scholar	rs864309702
google	rs864309702
pharmgkb	rs864309702
gwascentral	rs864309702
openSNP	rs864309702
23andMe	rs864309702
SNPshot	rs864309702
SNPdbe	rs864309702
MSV3d	rs864309702
GWAS Ctlg	rs864309702

Max Magnitude

0

ClinVar
Risk	rs864309702(-;-)
Alt	rs864309702(-;-)
Reference	Rs864309702(TTAG;TTAG)
Significance	Pathogenic
Disease	Congenital cataract
Variation	info
Gene	BCOR
CLNDBN	Congenital cataract
Reversed	1
HGVS	NC_000023.10:g.39933460_39933463delCTAA
CLNSRC
CLNACC	RCV000203315.1,