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rs4466998

From SNPedia

Orientationplus
Stabilizedplus
Make rs4466998(A;A)
Make rs4466998(A;C)
Make rs4466998(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position65008822
GeneFNTB, MAX
is asnp
is mentioned by
dbSNPrs4466998
ebirs4466998
HLIrs4466998
Exacrs4466998
Varsomers4466998
Maprs4466998
PheGenIrs4466998
hapmaprs4466998
1000 genomesrs4466998
hgdprs4466998
ensemblrs4466998
gopubmedrs4466998
geneviewrs4466998
scholarrs4466998
googlers4466998
pharmgkbrs4466998
gwascentralrs4466998
openSNPrs4466998
23andMers4466998
23andMe allrs4466998
SNP Nexus

SNPshotrs4466998
SNPdbers4466998
MSV3drs4466998
GWAS Ctlgrs4466998
GMAF0.4417
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular volume
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele A
P-val 5E-8
Odds Ratio 0 [0.001-0.003] fl increase


GET Evidence
rs4466998
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.585938
summary