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rs501764

From SNPedia

Orientationplus
Stabilizedplus
Make rs501764(G;G)
Make rs501764(G;T)
Make rs501764(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position8051071
GeneGALNTL1
is asnp
is mentioned by
dbSNPrs501764
ebirs501764
HLIrs501764
Exacrs501764
Varsomers501764
Maprs501764
PheGenIrs501764
hapmaprs501764
1000 genomesrs501764
hgdprs501764
ensemblrs501764
gopubmedrs501764
geneviewrs501764
scholarrs501764
googlers501764
pharmgkbrs501764
gwascentralrs501764
openSNPrs501764
23andMers501764
23andMe allrs501764
SNP Nexus

SNPshotrs501764
SNPdbers501764
MSV3drs501764
GWAS Ctlgrs501764
GMAF0.1042
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 21037568OA-icon.png] A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)


GET Evidence
NM_207423-S57R
aa_change Ser57Arg
aa_change_short S57R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.854167
summary



GWAS snp
PMID [PMID 24149102]
Trait Hodgkin's lymphoma
Title Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
Risk Allele C
P-val 4E-10
Odds Ratio 1.39 [NR]