rs886042842

Orientation

plus

Stabilized

plus

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

Chromosome

X

Position

40063035

Gene

BCOR

is a	snp
is	mentioned by
dbSNP	rs886042842
dbSNP (classic)	rs886042842
ClinGen	rs886042842
ebi	rs886042842
HLI	rs886042842
Exac	rs886042842
Gnomad	rs886042842
Varsome	rs886042842
LitVar	rs886042842
Map	rs886042842
PheGenI	rs886042842
Biobank	rs886042842
1000 genomes	rs886042842
hgdp	rs886042842
ensembl	rs886042842
geneview	rs886042842
scholar	rs886042842
google	rs886042842
pharmgkb	rs886042842
gwascentral	rs886042842
openSNP	rs886042842
23andMe	rs886042842
SNPshot	rs886042842
SNPdbe	rs886042842
MSV3d	rs886042842
GWAS Ctlg	rs886042842

Max Magnitude

0

ClinVar
Risk	rs886042842(-;-)
Alt	rs886042842(-;-)
Reference	Rs886042842(CT;CT)
Significance	Pathogenic
Disease	Oculofaciocardiodental syndrome
Variation	info
Gene	BCOR
CLNDBN	Oculofaciocardiodental syndrome
Reversed	0
HGVS	NC_000023.10:g.39922288_39922289delCT
CLNSRC
CLNACC	RCV000400462.1,