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rs6136489

From SNPedia

Orientationplus
Stabilizedplus
Make rs6136489(G;G)
Make rs6136489(G;T)
Make rs6136489(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position1943088
is asnp
is mentioned by
dbSNPrs6136489
ebirs6136489
HLIrs6136489
Exacrs6136489
Varsomers6136489
Maprs6136489
PheGenIrs6136489
hapmaprs6136489
1000 genomesrs6136489
hgdprs6136489
ensemblrs6136489
gopubmedrs6136489
geneviewrs6136489
scholarrs6136489
googlers6136489
pharmgkbrs6136489
gwascentralrs6136489
openSNPrs6136489
23andMers6136489
23andMe allrs6136489
SNP Nexus

SNPshotrs6136489
SNPdbers6136489
MSV3drs6136489
GWAS Ctlgrs6136489
GMAF0.4509
Max Magnitude
? (G;G) (G;T) (T;T) 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 T
P-val 8E-11
Odds Ratio 0.01 [0.006-0.014] fl increase


GET Evidence
rs6136489
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.476562
summary