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rs563507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs563507(A;A)
Make rs563507(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position34529060
GenePARD3
is asnp
is mentioned by
dbSNPrs563507
ebirs563507
HLIrs563507
Exacrs563507
Varsomers563507
Maprs563507
PheGenIrs563507
hapmaprs563507
1000 genomesrs563507
hgdprs563507
ensemblrs563507
gopubmedrs563507
geneviewrs563507
scholarrs563507
googlers563507
pharmgkbrs563507
gwascentralrs563507
openSNPrs563507
23andMers563507
23andMe allrs563507
SNP Nexus

SNPshotrs563507
SNPdbers563507
MSV3drs563507
GWAS Ctlgrs563507
GMAF0.06382
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19684603OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Germline genomic variants associated with childhood acute lymphoblastic leukemia
Risk Allele A
P-val 0.000009
Odds Ratio 2.00 [1.40-2.70]


GET Evidence
rs563507
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary