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rs172629

From SNPedia

Orientationplus
Stabilizedplus
Make rs172629(C;C)
Make rs172629(C;G)
Make rs172629(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position54541595
is asnp
is mentioned by
dbSNPrs172629
ebirs172629
HLIrs172629
Exacrs172629
Varsomers172629
Maprs172629
PheGenIrs172629
hapmaprs172629
1000 genomesrs172629
hgdprs172629
ensemblrs172629
gopubmedrs172629
geneviewrs172629
scholarrs172629
googlers172629
pharmgkbrs172629
gwascentralrs172629
openSNPrs172629
23andMers172629
23andMe allrs172629
SNP Nexus

SNPshotrs172629
SNPdbers172629
MSV3drs172629
GWAS Ctlgrs172629
GMAF0.2273
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular volume
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele G
P-val 1E-15
Odds Ratio 0 [0.003-0.006] fl decrease


GET Evidence
rs172629
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.206349
summary



GWAS snp
PMID [PMID 20139978]
Trait Mean corpuscular volume
Title Genome-wide association study of hematological and biochemical traits in a Japanese population.
Risk Allele C
P-val 1E-27
Odds Ratio .70 [0.573-0.824] unit decrease