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rs2075671

From SNPedia

Orientationminus
Stabilizedminus
Make rs2075671(C;C)
Make rs2075671(C;T)
Make rs2075671(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position100747483
GeneZAN
is asnp
is mentioned by
dbSNPrs2075671
ebirs2075671
HLIrs2075671
Exacrs2075671
Varsomers2075671
Maprs2075671
PheGenIrs2075671
hapmaprs2075671
1000 genomesrs2075671
hgdprs2075671
ensemblrs2075671
gopubmedrs2075671
geneviewrs2075671
scholarrs2075671
googlers2075671
pharmgkbrs2075671
gwascentralrs2075671
openSNPrs2075671
23andMers2075671
23andMe allrs2075671
SNP Nexus

SNPshotrs2075671
SNPdbers2075671
MSV3drs2075671
GWAS Ctlgrs2075671
GMAF0.1648
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Other erythrocyte phenotypes
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele A
P-val 1E-9
Odds Ratio 0 [0.005-0.009] 1 M cell/mm^3 increase


GET Evidence
rs2075671
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary