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rs2393967

From SNPedia

Orientationplus
Stabilizedplus
Make rs2393967(A;A)
Make rs2393967(A;C)
Make rs2393967(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position63373396
GeneJMJD1C, MIR1296
is asnp
is mentioned by
dbSNPrs2393967
ebirs2393967
HLIrs2393967
Exacrs2393967
Varsomers2393967
Maprs2393967
PheGenIrs2393967
hapmaprs2393967
1000 genomesrs2393967
hgdprs2393967
ensemblrs2393967
gopubmedrs2393967
geneviewrs2393967
scholarrs2393967
googlers2393967
pharmgkbrs2393967
gwascentralrs2393967
openSNPrs2393967
23andMers2393967
23andMe allrs2393967
SNP Nexus

SNPshotrs2393967
SNPdbers2393967
MSV3drs2393967
GWAS Ctlgrs2393967
GMAF0.2282
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 3E-21
Odds Ratio 0.01 [0.01-0.018] fl increase


GET Evidence
rs2393967
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.261905
summary