rs122445098

Orientation

minus

Stabilized

minus

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

Make rs122445098(A;G)

Make rs122445098(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

77558685

Gene

ATRX

is a	snp
is	mentioned by
dbSNP	rs122445098
dbSNP (classic)	rs122445098
ClinGen	rs122445098
ebi	rs122445098
HLI	rs122445098
Exac	rs122445098
Gnomad	rs122445098
Varsome	rs122445098
LitVar	rs122445098
Map	rs122445098
PheGenI	rs122445098
Biobank	rs122445098
1000 genomes	rs122445098
hgdp	rs122445098
ensembl	rs122445098
geneview	rs122445098
scholar	rs122445098
google	rs122445098
pharmgkb	rs122445098
gwascentral	rs122445098
openSNP	rs122445098
23andMe	rs122445098
SNPshot	rs122445098
SNPdbe	rs122445098
MSV3d	rs122445098
GWAS Ctlg	rs122445098

Max Magnitude

0

OMIM	300032
Desc
Variant	0007
Related	also

ClinVar
Risk	rs122445098(G;G)
Alt	rs122445098(G;G)
Reference	Rs122445098(A;A)
Significance	Pathogenic
Disease	ATR-X syndrome
Variation	info
Gene	ATRX
CLNDBN	ATR-X syndrome
Reversed	1
HGVS	NC_000023.10:g.76814156T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012493.16,