Have questions? Visit https://www.reddit.com/r/SNPedia

rs2660917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs2660917(C;C)
Make rs2660917(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position70960842
is asnp
is mentioned by
dbSNPrs2660917
ebirs2660917
HLIrs2660917
Exacrs2660917
Varsomers2660917
Maprs2660917
PheGenIrs2660917
hapmaprs2660917
1000 genomesrs2660917
hgdprs2660917
ensemblrs2660917
gopubmedrs2660917
geneviewrs2660917
scholarrs2660917
googlers2660917
pharmgkbrs2660917
gwascentralrs2660917
openSNPrs2660917
23andMers2660917
23andMe allrs2660917
SNP Nexus

SNPshotrs2660917
SNPdbers2660917
MSV3drs2660917
GWAS Ctlgrs2660917
GMAF0.2126
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 0.000008
Odds Ratio NR NR



GET Evidence
rs2660917
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.236842
summary