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rs797045592

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045592(C;T)
Make rs797045592(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128485741
GeneGATA2
is asnp
is mentioned by
dbSNPrs797045592
ebirs797045592
HLIrs797045592
Exacrs797045592
Varsomers797045592
Maprs797045592
PheGenIrs797045592
hapmaprs797045592
1000 genomesrs797045592
hgdprs797045592
ensemblrs797045592
gopubmedrs797045592
geneviewrs797045592
scholarrs797045592
googlers797045592
pharmgkbrs797045592
gwascentralrs797045592
openSNPrs797045592
23andMers797045592
23andMe allrs797045592
SNP Nexus

SNPshotrs797045592
SNPdbers797045592
MSV3drs797045592
GWAS Ctlgrs797045592
Max Magnitude0
ClinVar
Risk rs797045592(T;T)
Alt rs797045592(T;T)
Reference rs797045592(C;C)
Significance Probable-Pathogenic
Disease Leukemia
Variation info
Gene GATA2
CLNDBN Leukemia, acute myeloid, susceptibility to
Reversed 1
HGVS NC_000003.11:g.128204584G>A
CLNSRC
CLNACC RCV000193630.1,