rs122445107

Orientation

minus

Stabilized

minus

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

Make rs122445107(C;G)

Make rs122445107(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

77697589

Gene

ATRX

is a	snp
is	mentioned by
dbSNP	rs122445107
dbSNP (classic)	rs122445107
ClinGen	rs122445107
ebi	rs122445107
HLI	rs122445107
Exac	rs122445107
Gnomad	rs122445107
Varsome	rs122445107
LitVar	rs122445107
Map	rs122445107
PheGenI	rs122445107
Biobank	rs122445107
1000 genomes	rs122445107
hgdp	rs122445107
ensembl	rs122445107
geneview	rs122445107
scholar	rs122445107
google	rs122445107
pharmgkb	rs122445107
gwascentral	rs122445107
openSNP	rs122445107
23andMe	rs122445107
SNPshot	rs122445107
SNPdbe	rs122445107
MSV3d	rs122445107
GWAS Ctlg	rs122445107

Max Magnitude

0

OMIM	300032
Desc
Variant	0021
Related	also

ClinVar
Risk	rs122445107(G;G)
Alt	rs122445107(G;G)
Reference	Rs122445107(C;C)
Significance	Pathogenic
Disease	Acquired hemoglobin H disease
Variation	info
Gene	ATRX
CLNDBN	Acquired hemoglobin H disease
Reversed	1
HGVS	NC_000023.10:g.76953077G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012507.4,