rs104894746

Orientation

minus

Stabilized

minus

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

Make rs104894746(G;T)

Make rs104894746(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

25010274

Gene

ARX

is a	snp
is	mentioned by
dbSNP	rs104894746
dbSNP (classic)	rs104894746
ClinGen	rs104894746
ebi	rs104894746
HLI	rs104894746
Exac	rs104894746
Gnomad	rs104894746
Varsome	rs104894746
LitVar	rs104894746
Map	rs104894746
PheGenI	rs104894746
Biobank	rs104894746
1000 genomes	rs104894746
hgdp	rs104894746
ensembl	rs104894746
geneview	rs104894746
scholar	rs104894746
google	rs104894746
pharmgkb	rs104894746
gwascentral	rs104894746
openSNP	rs104894746
23andMe	rs104894746
SNPshot	rs104894746
SNPdbe	rs104894746
MSV3d	rs104894746
GWAS Ctlg	rs104894746

Max Magnitude

0

OMIM	300382
Desc
Variant	0016
Related	also

ClinVar
Risk	rs104894746(A;A) rs104894746(T;T)
Alt	rs104894746(A;A) rs104894746(T;T)
Reference	Rs104894746(G;G)
Significance	Pathogenic
Disease	Hydranencephaly with abnormal genitalia not provided
Variation	info
Gene	ARX
CLNDBN	Hydranencephaly with abnormal genitalia not provided
Reversed	1
HGVS	NC_000023.10:g.25028391C>A; NC_000023.10:g.25028391C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011952.18, RCV000442107.1,