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rs2138852

From SNPedia

Orientationminus
Stabilizedminus
Make rs2138852(A;A)
Make rs2138852(A;G)
Make rs2138852(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position29376331
is asnp
is mentioned by
dbSNPrs2138852
ebirs2138852
HLIrs2138852
Exacrs2138852
Varsomers2138852
Maprs2138852
PheGenIrs2138852
hapmaprs2138852
1000 genomesrs2138852
hgdprs2138852
ensemblrs2138852
gopubmedrs2138852
geneviewrs2138852
scholarrs2138852
googlers2138852
pharmgkbrs2138852
gwascentralrs2138852
openSNPrs2138852
23andMers2138852
23andMe allrs2138852
SNP Nexus

SNPshotrs2138852
SNPdbers2138852
MSV3drs2138852
GWAS Ctlgrs2138852
GMAF0.2654
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19110211OA-icon.png] rs7961894, rs12485738 and rs2138852 together accounted for 4%-5% of the variance in mean platelet volume, which is increased in myocardial and cerebral infarction and is an independent and strong predictor for postevent morbidity and mortality
OMIM612575
DescMEAN PLATELET VOLUME QUANTITATIVE TRAIT LOCUS 3; MPVQTL3
Variant
Relatedalso
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 1E-22
Odds Ratio 0.02 [0.012-0.020] fl increase




GET Evidence
rs2138852
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.703125
summary