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rs10506328

From SNPedia

Orientationplus
Stabilizedplus
Make rs10506328(A;A)
Make rs10506328(A;C)
Make rs10506328(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position54293448
GeneNFE2
is asnp
is mentioned by
dbSNPrs10506328
ebirs10506328
HLIrs10506328
Exacrs10506328
Varsomers10506328
Maprs10506328
PheGenIrs10506328
hapmaprs10506328
1000 genomesrs10506328
hgdprs10506328
ensemblrs10506328
gopubmedrs10506328
geneviewrs10506328
scholarrs10506328
googlers10506328
pharmgkbrs10506328
gwascentralrs10506328
openSNPrs10506328
23andMers10506328
23andMe allrs10506328
SNP Nexus

SNPshotrs10506328
SNPdbers10506328
MSV3drs10506328
GWAS Ctlgrs10506328
GMAF0.1703
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait MPV
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele A
P-val 5E-7
Odds Ratio 0.01 [0.004-0.012] fl increase


GET Evidence
rs10506328
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.828125
summary



GWAS snp
PMID [PMID 24026423OA-icon.png]
Trait Mean platelet volume
Title A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Risk Allele C
P-val 2E-9
Odds Ratio .09 [NR] unit decrease