rs267607188

Orientation

minus

Stabilized

minus

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

Make rs267607188(C;T)

Make rs267607188(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

53254856

Gene

IQSEC2

is a	snp
is	mentioned by
dbSNP	rs267607188
dbSNP (classic)	rs267607188
ClinGen	rs267607188
ebi	rs267607188
HLI	rs267607188
Exac	rs267607188
Gnomad	rs267607188
Varsome	rs267607188
LitVar	rs267607188
Map	rs267607188
PheGenI	rs267607188
Biobank	rs267607188
1000 genomes	rs267607188
hgdp	rs267607188
ensembl	rs267607188
geneview	rs267607188
scholar	rs267607188
google	rs267607188
pharmgkb	rs267607188
gwascentral	rs267607188
openSNP	rs267607188
23andMe	rs267607188
SNPshot	rs267607188
SNPdbe	rs267607188
MSV3d	rs267607188
GWAS Ctlg	rs267607188

Max Magnitude

0

ClinVar
Risk	rs267607188(T;T)
Alt	rs267607188(T;T)
Reference	Rs267607188(C;C)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	IQSEC2
CLNDBN	Mental retardation, X-linked 1
Reversed	1
HGVS	NC_000023.10:g.53284038G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011612.4,