rs121908584

Orientation

plus

Stabilized

plus

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

Make rs121908584(A;G)

Make rs121908584(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

95535383

Gene	GLRX5, SCARNA13, SNHG10

is a	snp
is	mentioned by
dbSNP	rs121908584
dbSNP (classic)	rs121908584
ClinGen	rs121908584
ebi	rs121908584
HLI	rs121908584
Exac	rs121908584
Gnomad	rs121908584
Varsome	rs121908584
LitVar	rs121908584
Map	rs121908584
PheGenI	rs121908584
Biobank	rs121908584
1000 genomes	rs121908584
hgdp	rs121908584
ensembl	rs121908584
geneview	rs121908584
scholar	rs121908584
google	rs121908584
pharmgkb	rs121908584
gwascentral	rs121908584
openSNP	rs121908584
23andMe	rs121908584
SNPshot	rs121908584
SNPdbe	rs121908584
MSV3d	rs121908584
GWAS Ctlg	rs121908584

Max Magnitude

0

OMIM	609588
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908584(G;G)
Alt	rs121908584(G;G)
Reference	Rs121908584(A;A)
Significance	Pathogenic
Disease	Anemia
Variation	info
Gene	SNHG10 SCARNA13 GLRX5
CLNDBN	Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive
Reversed	0
HGVS	NC_000014.8:g.96001720A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001673.3,