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rs4406737

From SNPedia

Orientationplus
Stabilizedplus
Make rs4406737(A;A)
Make rs4406737(A;G)
Make rs4406737(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position88999967
GeneFAS
is asnp
is mentioned by
dbSNPrs4406737
dbSNP (classic)rs4406737
ClinGenrs4406737
ebirs4406737
HLIrs4406737
Exacrs4406737
Gnomadrs4406737
Varsomers4406737
LitVarrs4406737
Maprs4406737
PheGenIrs4406737
Biobankrs4406737
1000 genomesrs4406737
hgdprs4406737
ensemblrs4406737
geneviewrs4406737
scholarrs4406737
googlers4406737
pharmgkbrs4406737
gwascentralrs4406737
openSNPrs4406737
23andMers4406737
SNPshotrs4406737
SNPdbers4406737
MSV3drs4406737
GWAS Ctlgrs4406737
GMAF0.4922
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23770605OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele G
P-val 1E-14
Odds Ratio 1.27 [1.19-1.33]