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rs587776963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776963(A;A)
Make rs587776963(A;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position119245796
GeneSTEAP3
is asnp
is mentioned by
dbSNPrs587776963
ebirs587776963
HLIrs587776963
Exacrs587776963
Varsomers587776963
Maprs587776963
PheGenIrs587776963
hapmaprs587776963
1000 genomesrs587776963
hgdprs587776963
ensemblrs587776963
gopubmedrs587776963
geneviewrs587776963
scholarrs587776963
googlers587776963
pharmgkbrs587776963
gwascentralrs587776963
openSNPrs587776963
23andMers587776963
23andMe allrs587776963
SNP Nexus

SNPshotrs587776963
SNPdbers587776963
MSV3drs587776963
GWAS Ctlgrs587776963
Max Magnitude0
ClinVar
Risk rs587776963(A;A)
Alt rs587776963(A;A)
Reference rs587776963(C;C)
Significance Pathogenic
Disease Hypochromic microcytic anemia with iron overload 2
Variation info
Gene STEAP3-AS1 STEAP3
CLNDBN Hypochromic microcytic anemia with iron overload 2
Reversed 0
HGVS NC_000002.11:g.120003372C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043521.4,