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rs10500991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10500991(C;T)
Make rs10500991(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position24828020
GeneLUZP2
is asnp
is mentioned by
dbSNPrs10500991
ebirs10500991
HLIrs10500991
Exacrs10500991
Varsomers10500991
Maprs10500991
PheGenIrs10500991
hapmaprs10500991
1000 genomesrs10500991
hgdprs10500991
ensemblrs10500991
gopubmedrs10500991
geneviewrs10500991
scholarrs10500991
googlers10500991
pharmgkbrs10500991
gwascentralrs10500991
openSNPrs10500991
23andMers10500991
23andMe allrs10500991
SNP Nexus

SNPshotrs10500991
SNPdbers10500991
MSV3drs10500991
GWAS Ctlgrs10500991
GMAF0.08264
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19084217OA-icon.png]
Trait Serum markers of iron status
Title Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels
Risk Allele
P-val 0.000002
Odds Ratio NR NR



GET Evidence
rs10500991
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0625
summary