rs267607187

Orientation

minus

Stabilized

minus

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

Make rs267607187(A;C)

Make rs267607187(C;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

53248778

Gene

IQSEC2

is a	snp
is	mentioned by
dbSNP	rs267607187
dbSNP (classic)	rs267607187
ClinGen	rs267607187
ebi	rs267607187
HLI	rs267607187
Exac	rs267607187
Gnomad	rs267607187
Varsome	rs267607187
LitVar	rs267607187
Map	rs267607187
PheGenI	rs267607187
Biobank	rs267607187
1000 genomes	rs267607187
hgdp	rs267607187
ensembl	rs267607187
geneview	rs267607187
scholar	rs267607187
google	rs267607187
pharmgkb	rs267607187
gwascentral	rs267607187
openSNP	rs267607187
23andMe	rs267607187
SNPshot	rs267607187
SNPdbe	rs267607187
MSV3d	rs267607187
GWAS Ctlg	rs267607187

Max Magnitude

0

ClinVar
Risk	rs267607187(C;C)
Alt	rs267607187(C;C)
Reference	Rs267607187(A;A)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	IQSEC2
CLNDBN	Mental retardation, X-linked 18
Reversed	1
HGVS	NC_000023.10:g.53277960T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011610.9,