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rs62527607

From SNPedia

Orientationplus
Stabilizedplus
Make rs62527607(G;G)
Make rs62527607(G;T)
Make rs62527607(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position103141321
GeneBAALC
is asnp
is mentioned by
dbSNPrs62527607
ebirs62527607
HLIrs62527607
Exacrs62527607
Varsomers62527607
Maprs62527607
PheGenIrs62527607
hapmaprs62527607
1000 genomesrs62527607
hgdprs62527607
ensemblrs62527607
gopubmedrs62527607
geneviewrs62527607
scholarrs62527607
googlers62527607
pharmgkbrs62527607
gwascentralrs62527607
openSNPrs62527607
23andMers62527607
23andMe allrs62527607
SNP Nexus

SNPshotrs62527607
SNPdbers62527607
MSV3drs62527607
GWAS Ctlgrs62527607
GMAF0.1019
Max Magnitude
http://medicalxpress.com/news/2012-05-inherited-dna-overactive-leukemia-gene.html rs62527607(T) – which creates a RUNX1 binding site in the BAALC promoter region. This gene is often overactive, or overexpressed, in people with acute myeloid leukemia or acute lymphoblastic leukemia, and it indicates that the disease is likely to respond poorly to standard therapy.

[PMID 22493267OA-icon.png] Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemia.

news miR-3151, not BAALC is probably the risk factor for AML. [PMID 27372260] Evaluation of rs62527607 [GT] single nucleotide polymorphism located in BAALC gene in children with acute leukemia using mismatch PCR-RFLP.