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rs2191566

From SNPedia

Orientationminus
Stabilizedminus
Make rs2191566(A;A)
Make rs2191566(A;C)
Make rs2191566(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position44007237
GeneZNF230
is asnp
is mentioned by
dbSNPrs2191566
ebirs2191566
HLIrs2191566
Exacrs2191566
Varsomers2191566
Maprs2191566
PheGenIrs2191566
hapmaprs2191566
1000 genomesrs2191566
hgdprs2191566
ensemblrs2191566
gopubmedrs2191566
geneviewrs2191566
scholarrs2191566
googlers2191566
pharmgkbrs2191566
gwascentralrs2191566
openSNPrs2191566
23andMers2191566
23andMe allrs2191566
SNP Nexus

SNPshotrs2191566
SNPdbers2191566
MSV3drs2191566
GWAS Ctlgrs2191566
GMAF0.4697
Max Magnitude
? (A;A) (A;C) (C;C) 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 G
P-val 4E-7
Odds Ratio 1.52 [1.20-1.70]


GET Evidence
rs2191566
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.555556
summary



[PMID 26177813] Replication analysis confirms the association of several variants with acute myeloid leukemia in Chinese population