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rs9374080

From SNPedia

Orientationplus
Stabilizedplus
Make rs9374080(C;C)
Make rs9374080(C;T)
Make rs9374080(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position109295217
GeneCCDC162P
is asnp
is mentioned by
dbSNPrs9374080
ebirs9374080
HLIrs9374080
Exacrs9374080
Varsomers9374080
Maprs9374080
PheGenIrs9374080
hapmaprs9374080
1000 genomesrs9374080
hgdprs9374080
ensemblrs9374080
gopubmedrs9374080
geneviewrs9374080
scholarrs9374080
googlers9374080
pharmgkbrs9374080
gwascentralrs9374080
openSNPrs9374080
23andMers9374080
23andMe allrs9374080
SNP Nexus

SNPshotrs9374080
SNPdbers9374080
MSV3drs9374080
GWAS Ctlgrs9374080
GMAF0.3049
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular volume
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele C
P-val 4E-10
Odds Ratio 0 [0.002-0.003] fl decrease


GET Evidence
rs9374080
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary