rs587783199

Orientation

minus

Stabilized

minus

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

Make rs587783199(-;-)

Make rs587783199(-;CAGCGGCCGCCACGGCCACGGCGGGTCCACGCGG)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

25013627

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs587783199
dbSNP (classic)	rs587783199
ClinGen	rs587783199
ebi	rs587783199
HLI	rs587783199
Exac	rs587783199
Gnomad	rs587783199
Varsome	rs587783199
LitVar	rs587783199
Map	rs587783199
PheGenI	rs587783199
Biobank	rs587783199
1000 genomes	rs587783199
hgdp	rs587783199
ensembl	rs587783199
geneview	rs587783199
scholar	rs587783199
google	rs587783199
pharmgkb	rs587783199
gwascentral	rs587783199
openSNP	rs587783199
23andMe	rs587783199
SNPshot	rs587783199
SNPdbe	rs587783199
MSV3d	rs587783199
GWAS Ctlg	rs587783199

Max Magnitude

0

ClinVar
Risk	rs587783199(-;-)
Alt	rs587783199(-;-)
Reference	Rs587783199(CAGCGGCCGCCACGGCCACGGCGGGTCCACGCGG;CAGCGGCCGCCACGGCCACGGCGGGTCCACGCGG)
Significance	Pathogenic
Disease	Lissencephaly 2
Variation	info
Gene	ARX
CLNDBN	Lissencephaly 2, X-linked
Reversed	1
HGVS	NC_000023.10:g.25031744_25031777del34
CLNSRC
CLNACC	RCV000145055.1,