rs122445097

Orientation

minus

Stabilized

minus

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

Make rs122445097(C;C)

Make rs122445097(C;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

77574326

Gene

ATRX

is a	snp
is	mentioned by
dbSNP	rs122445097
dbSNP (classic)	rs122445097
ClinGen	rs122445097
ebi	rs122445097
HLI	rs122445097
Exac	rs122445097
Gnomad	rs122445097
Varsome	rs122445097
LitVar	rs122445097
Map	rs122445097
PheGenI	rs122445097
Biobank	rs122445097
1000 genomes	rs122445097
hgdp	rs122445097
ensembl	rs122445097
geneview	rs122445097
scholar	rs122445097
google	rs122445097
pharmgkb	rs122445097
gwascentral	rs122445097
openSNP	rs122445097
23andMe	rs122445097
SNPshot	rs122445097
SNPdbe	rs122445097
MSV3d	rs122445097
GWAS Ctlg	rs122445097

Max Magnitude

0

OMIM	300032
Desc
Variant	0006
Related	also

ClinVar
Risk	rs122445097(C;C)
Alt	rs122445097(C;C)
Reference	Rs122445097(T;T)
Significance	Pathogenic
Disease	ATR-X syndrome
Variation	info
Gene	ATRX
CLNDBN	ATR-X syndrome
Reversed	1
HGVS	NC_000023.10:g.76829791A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012492.14,