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rs17270561

From SNPedia

Orientationplus
Stabilizedplus
Make rs17270561(A;A)
Make rs17270561(A;C)
Make rs17270561(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position25820211
GeneSLC17A1
is asnp
is mentioned by
dbSNPrs17270561
ebirs17270561
HLIrs17270561
Exacrs17270561
Varsomers17270561
Maprs17270561
PheGenIrs17270561
hapmaprs17270561
1000 genomesrs17270561
hgdprs17270561
ensemblrs17270561
gopubmedrs17270561
geneviewrs17270561
scholarrs17270561
googlers17270561
pharmgkbrs17270561
gwascentralrs17270561
openSNPrs17270561
23andMers17270561
23andMe allrs17270561
SNP Nexus

SNPshotrs17270561
SNPdbers17270561
MSV3drs17270561
GWAS Ctlgrs17270561
GMAF0.1552
Max Magnitude
? (A;A) (A;C) (C;C) 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 5E-7
Odds Ratio NR NR



GET Evidence
rs17270561
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary