rs727503826

Orientation

minus

Stabilized

minus

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

Make rs727503826(A;A)

Make rs727503826(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

40074570

Gene

BCOR

is a	snp
is	mentioned by
dbSNP	rs727503826
dbSNP (classic)	rs727503826
ClinGen	rs727503826
ebi	rs727503826
HLI	rs727503826
Exac	rs727503826
Gnomad	rs727503826
Varsome	rs727503826
LitVar	rs727503826
Map	rs727503826
PheGenI	rs727503826
Biobank	rs727503826
1000 genomes	rs727503826
hgdp	rs727503826
ensembl	rs727503826
geneview	rs727503826
scholar	rs727503826
google	rs727503826
pharmgkb	rs727503826
gwascentral	rs727503826
openSNP	rs727503826
23andMe	rs727503826
SNPshot	rs727503826
SNPdbe	rs727503826
MSV3d	rs727503826
GWAS Ctlg	rs727503826

Max Magnitude

0

ClinVar
Risk	rs727503826(A;A)
Alt	rs727503826(A;A)
Reference	Rs727503826(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	BCOR
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.39933823G>T
CLNSRC
CLNACC	RCV000152859.3,