rs151177114

Orientation

plus

Stabilized

plus

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

Make rs151177114(C;C)

Make rs151177114(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

40074322

Gene

BCOR

is a	snp
is	mentioned by
dbSNP	rs151177114
dbSNP (classic)	rs151177114
ClinGen	rs151177114
ebi	rs151177114
HLI	rs151177114
Exac	rs151177114
Gnomad	rs151177114
Varsome	rs151177114
LitVar	rs151177114
Map	rs151177114
PheGenI	rs151177114
Biobank	rs151177114
1000 genomes	rs151177114
hgdp	rs151177114
ensembl	rs151177114
geneview	rs151177114
scholar	rs151177114
google	rs151177114
pharmgkb	rs151177114
gwascentral	rs151177114
openSNP	rs151177114
23andMe	rs151177114
SNPshot	rs151177114
SNPdbe	rs151177114
MSV3d	rs151177114
GWAS Ctlg	rs151177114

Max Magnitude

0

ClinVar
Risk	rs151177114(C;C)
Alt	rs151177114(C;C)
Reference	Rs151177114(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	BCOR
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.39933575G>A
CLNSRC
CLNACC	RCV000494521.1,