rs1060499660

Orientation

minus

Stabilized

minus

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

Make rs1060499660(C;C)

Make rs1060499660(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

53248219

Gene

IQSEC2

is a	snp
is	mentioned by
dbSNP	rs1060499660
dbSNP (classic)	rs1060499660
ClinGen	rs1060499660
ebi	rs1060499660
HLI	rs1060499660
Exac	rs1060499660
Gnomad	rs1060499660
Varsome	rs1060499660
LitVar	rs1060499660
Map	rs1060499660
PheGenI	rs1060499660
Biobank	rs1060499660
1000 genomes	rs1060499660
hgdp	rs1060499660
ensembl	rs1060499660
geneview	rs1060499660
scholar	rs1060499660
google	rs1060499660
pharmgkb	rs1060499660
gwascentral	rs1060499660
openSNP	rs1060499660
23andMe	rs1060499660
SNPshot	rs1060499660
SNPdbe	rs1060499660
MSV3d	rs1060499660
GWAS Ctlg	rs1060499660

Max Magnitude

0

ClinVar
Risk	rs1060499660(C;C)
Alt	rs1060499660(C;C)
Reference	Rs1060499660(T;T)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	IQSEC2
CLNDBN	Mental retardation, X-linked 1
Reversed	1
HGVS	NC_000023.10:g.53277401A>G
CLNSRC
CLNACC	RCV000449548.1,