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rs628751

From SNPedia

Orientationplus
Stabilizedplus
Make rs628751(A;A)
Make rs628751(A;C)
Make rs628751(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position139517282
is asnp
is mentioned by
dbSNPrs628751
ebirs628751
HLIrs628751
Exacrs628751
Varsomers628751
Maprs628751
PheGenIrs628751
hapmaprs628751
1000 genomesrs628751
hgdprs628751
ensemblrs628751
gopubmedrs628751
geneviewrs628751
scholarrs628751
googlers628751
pharmgkbrs628751
gwascentralrs628751
openSNPrs628751
23andMers628751
23andMe allrs628751
SNP Nexus

SNPshotrs628751
SNPdbers628751
MSV3drs628751
GWAS Ctlgrs628751
GMAF0.3531
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular hemoglobin
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele C
P-val 1E-17
Odds Ratio 0 [0.003-0.005] pg decrease


GET Evidence
rs628751
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency
summary