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rs797045591

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045591(C;C)
Make rs797045591(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128481908
GeneGATA2
is asnp
is mentioned by
dbSNPrs797045591
ebirs797045591
HLIrs797045591
Exacrs797045591
Varsomers797045591
Maprs797045591
PheGenIrs797045591
hapmaprs797045591
1000 genomesrs797045591
hgdprs797045591
ensemblrs797045591
gopubmedrs797045591
geneviewrs797045591
scholarrs797045591
googlers797045591
pharmgkbrs797045591
gwascentralrs797045591
openSNPrs797045591
23andMers797045591
23andMe allrs797045591
SNP Nexus

SNPshotrs797045591
SNPdbers797045591
MSV3drs797045591
GWAS Ctlgrs797045591
Max Magnitude0
ClinVar
Risk rs797045591(C;C)
Alt rs797045591(C;C)
Reference rs797045591(T;T)
Significance Probable-Pathogenic
Disease Leukemia
Variation info
Gene GATA2
CLNDBN Leukemia, acute myeloid, susceptibility to
Reversed 1
HGVS NC_000003.11:g.128200751A>G
CLNSRC
CLNACC RCV000194241.1,