rs369432845

Orientation

plus

Stabilized

plus

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

Make rs369432845(G;T)

Make rs369432845(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

40062275

Gene

BCOR

is a	snp
is	mentioned by
dbSNP	rs369432845
dbSNP (classic)	rs369432845
ClinGen	rs369432845
ebi	rs369432845
HLI	rs369432845
Exac	rs369432845
Gnomad	rs369432845
Varsome	rs369432845
LitVar	rs369432845
Map	rs369432845
PheGenI	rs369432845
Biobank	rs369432845
1000 genomes	rs369432845
hgdp	rs369432845
ensembl	rs369432845
geneview	rs369432845
scholar	rs369432845
google	rs369432845
pharmgkb	rs369432845
gwascentral	rs369432845
openSNP	rs369432845
23andMe	rs369432845
SNPshot	rs369432845
SNPdbe	rs369432845
MSV3d	rs369432845
GWAS Ctlg	rs369432845

Max Magnitude

0

ClinVar
Risk	rs369432845(A;A) rs369432845(T;T)
Alt	rs369432845(A;A) rs369432845(T;T)
Reference	Rs369432845(G;G)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	BCOR
CLNDBN	Abnormality of brain morphology
Reversed	0
HGVS	NC_000023.10:g.39921528G>T
CLNSRC
CLNACC	RCV000454264.1,