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rs4947019

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4947019(C;G)
Make rs4947019(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position109768846
GeneFIG4
is asnp
is mentioned by
dbSNPrs4947019
ebirs4947019
HLIrs4947019
Exacrs4947019
Varsomers4947019
Maprs4947019
PheGenIrs4947019
hapmaprs4947019
1000 genomesrs4947019
hgdprs4947019
ensemblrs4947019
gopubmedrs4947019
geneviewrs4947019
scholarrs4947019
googlers4947019
pharmgkbrs4947019
gwascentralrs4947019
openSNPrs4947019
23andMers4947019
23andMe allrs4947019
SNP Nexus

SNPshotrs4947019
SNPdbers4947019
MSV3drs4947019
GWAS Ctlgrs4947019
GMAF0.1391
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait Hematological parameters
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele G
P-val 0.000008
Odds Ratio 0.01 [0.003-0.011] fl decrease


GET Evidence
rs4947019
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary