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rs1473247

From SNPedia

Orientationplus
Stabilizedplus
Make rs1473247(C;C)
Make rs1473247(C;T)
Make rs1473247(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position159176563
GeneRNF145
is asnp
is mentioned by
dbSNPrs1473247
ebirs1473247
HLIrs1473247
Exacrs1473247
Varsomers1473247
Maprs1473247
PheGenIrs1473247
hapmaprs1473247
1000 genomesrs1473247
hgdprs1473247
ensemblrs1473247
gopubmedrs1473247
geneviewrs1473247
scholarrs1473247
googlers1473247
pharmgkbrs1473247
gwascentralrs1473247
openSNPrs1473247
23andMers1473247
23andMe allrs1473247
SNP Nexus

SNPshotrs1473247
SNPdbers1473247
MSV3drs1473247
GWAS Ctlgrs1473247
GMAF0.4376
Max Magnitude
? (C;C) (C;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 C
P-val 3E-7
Odds Ratio 0.01 [0.004-0.012] fl decrease


GET Evidence
rs1473247
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.47619
summary