rs730882186

Orientation

minus

Stabilized

minus

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

Make rs730882186(-;A)

Make rs730882186(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

80735165

Gene

BRWD3

is a	snp
is	mentioned by
dbSNP	rs730882186
dbSNP (classic)	rs730882186
ClinGen	rs730882186
ebi	rs730882186
HLI	rs730882186
Exac	rs730882186
Gnomad	rs730882186
Varsome	rs730882186
LitVar	rs730882186
Map	rs730882186
PheGenI	rs730882186
Biobank	rs730882186
1000 genomes	rs730882186
hgdp	rs730882186
ensembl	rs730882186
geneview	rs730882186
scholar	rs730882186
google	rs730882186
pharmgkb	rs730882186
gwascentral	rs730882186
openSNP	rs730882186
23andMe	rs730882186
SNPshot	rs730882186
SNPdbe	rs730882186
MSV3d	rs730882186
GWAS Ctlg	rs730882186

Max Magnitude

0

ClinVar
Risk	rs730882186(A;A)
Alt	rs730882186(A;A)
Reference	Rs730882186(-;-)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	BRWD3
CLNDBN	Mental retardation, X-linked 93
Reversed	1
HGVS	NC_000023.10:g.79990665dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011550.7,