rs122445096

Orientation

minus

Stabilized

minus

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

Make rs122445096(A;T)

Make rs122445096(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

77593702

Gene

ATRX

is a	snp
is	mentioned by
dbSNP	rs122445096
dbSNP (classic)	rs122445096
ClinGen	rs122445096
ebi	rs122445096
HLI	rs122445096
Exac	rs122445096
Gnomad	rs122445096
Varsome	rs122445096
LitVar	rs122445096
Map	rs122445096
PheGenI	rs122445096
Biobank	rs122445096
1000 genomes	rs122445096
hgdp	rs122445096
ensembl	rs122445096
geneview	rs122445096
scholar	rs122445096
google	rs122445096
pharmgkb	rs122445096
gwascentral	rs122445096
openSNP	rs122445096
23andMe	rs122445096
SNPshot	rs122445096
SNPdbe	rs122445096
MSV3d	rs122445096
GWAS Ctlg	rs122445096

Max Magnitude

0

OMIM	300032
Desc
Variant	0005
Related	also

ClinVar
Risk	rs122445096(T;T)
Alt	rs122445096(T;T)
Reference	Rs122445096(A;A)
Significance	Pathogenic
Disease	ATR-X syndrome
Variation	info
Gene	ATRX
CLNDBN	ATR-X syndrome
Reversed	1
HGVS	NC_000023.10:g.76849172T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012491.14,