rs748074364

Orientation

plus

Stabilized

plus

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

Make rs748074364(-;G)

Make rs748074364(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

X

Position

40053925

Gene

BCOR

is a	snp
is	mentioned by
dbSNP	rs748074364
dbSNP (classic)	rs748074364
ClinGen	rs748074364
ebi	rs748074364
HLI	rs748074364
Exac	rs748074364
Gnomad	rs748074364
Varsome	rs748074364
LitVar	rs748074364
Map	rs748074364
PheGenI	rs748074364
Biobank	rs748074364
1000 genomes	rs748074364
hgdp	rs748074364
ensembl	rs748074364
geneview	rs748074364
scholar	rs748074364
google	rs748074364
pharmgkb	rs748074364
gwascentral	rs748074364
openSNP	rs748074364
23andMe	rs748074364
SNPshot	rs748074364
SNPdbe	rs748074364
MSV3d	rs748074364
GWAS Ctlg	rs748074364

Max Magnitude

0

ClinVar
Risk	rs748074364(G;G)
Alt	rs748074364(G;G)
Reference	Rs748074364(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	BCOR
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.39913179dupG
CLNSRC
CLNACC	RCV000346544.1,