rs122445094

Orientation

minus

Stabilized

minus

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

Make rs122445094(C;C)

Make rs122445094(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

77633682

Gene

ATRX

is a	snp
is	mentioned by
dbSNP	rs122445094
dbSNP (classic)	rs122445094
ClinGen	rs122445094
ebi	rs122445094
HLI	rs122445094
Exac	rs122445094
Gnomad	rs122445094
Varsome	rs122445094
LitVar	rs122445094
Map	rs122445094
PheGenI	rs122445094
Biobank	rs122445094
1000 genomes	rs122445094
hgdp	rs122445094
ensembl	rs122445094
geneview	rs122445094
scholar	rs122445094
google	rs122445094
pharmgkb	rs122445094
gwascentral	rs122445094
openSNP	rs122445094
23andMe	rs122445094
SNPshot	rs122445094
SNPdbe	rs122445094
MSV3d	rs122445094
GWAS Ctlg	rs122445094

Max Magnitude

0

OMIM	300032
Desc
Variant	0002
Related	also

ClinVar
Risk	rs122445094(C;C)
Alt	rs122445094(C;C)
Reference	Rs122445094(T;T)
Significance	Pathogenic
Disease	ATR-X syndrome
Variation	info
Gene	ATRX
CLNDBN	ATR-X syndrome
Reversed	1
HGVS	NC_000023.10:g.76889170A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012488.24,