rs863224851

Orientation

minus

Stabilized

minus

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

Make rs863224851(G;G)

Make rs863224851(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

80682607

Gene

BRWD3

is a	snp
is	mentioned by
dbSNP	rs863224851
dbSNP (classic)	rs863224851
ClinGen	rs863224851
ebi	rs863224851
HLI	rs863224851
Exac	rs863224851
Gnomad	rs863224851
Varsome	rs863224851
LitVar	rs863224851
Map	rs863224851
PheGenI	rs863224851
Biobank	rs863224851
1000 genomes	rs863224851
hgdp	rs863224851
ensembl	rs863224851
geneview	rs863224851
scholar	rs863224851
google	rs863224851
pharmgkb	rs863224851
gwascentral	rs863224851
openSNP	rs863224851
23andMe	rs863224851
SNPshot	rs863224851
SNPdbe	rs863224851
MSV3d	rs863224851
GWAS Ctlg	rs863224851

Max Magnitude

0

ClinVar
Risk	rs863224851(G;G)
Alt	rs863224851(G;G)
Reference	Rs863224851(T;T)
Significance	Probable-Pathogenic
Disease	Mental retardation
Variation	info
Gene	BRWD3
CLNDBN	Mental retardation, X-linked 93
Reversed	1
HGVS	NC_000023.10:g.79938106A>C
CLNSRC
CLNACC	RCV000199586.1,