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rs121908584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908584(A;G)
Make rs121908584(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position95535383
GeneGLRX5, SCARNA13, SNHG10
is asnp
is mentioned by
dbSNPrs121908584
ebirs121908584
HLIrs121908584
Exacrs121908584
Varsomers121908584
Maprs121908584
PheGenIrs121908584
hapmaprs121908584
1000 genomesrs121908584
hgdprs121908584
ensemblrs121908584
gopubmedrs121908584
geneviewrs121908584
scholarrs121908584
googlers121908584
pharmgkbrs121908584
gwascentralrs121908584
openSNPrs121908584
23andMers121908584
23andMe allrs121908584
SNP Nexus

SNPshotrs121908584
SNPdbers121908584
MSV3drs121908584
GWAS Ctlgrs121908584
Max Magnitude0
OMIM609588
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908584(G;G)
Alt rs121908584(G;G)
Reference rs121908584(A;A)
Significance Pathogenic
Disease Anemia
Variation info
Gene SCARNA13 SNHG10 GLRX5
CLNDBN Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive
Reversed 0
HGVS NC_000014.8:g.96001720A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001673.2,