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rs587776834

From SNPedia

Orientationplus
Geno Mag Summary
(ATC;ATC) 0 common in clinvar
(GATT;GATT) 0 common in clinvar
Make rs587776834(-;-)
Make rs587776834(-;ATC)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position28034140
GeneFLT3
is asnp
is mentioned by
dbSNPrs587776834
ebirs587776834
HLIrs587776834
Exacrs587776834
Varsomers587776834
Maprs587776834
PheGenIrs587776834
hapmaprs587776834
1000 genomesrs587776834
hgdprs587776834
ensemblrs587776834
gopubmedrs587776834
geneviewrs587776834
scholarrs587776834
googlers587776834
pharmgkbrs587776834
gwascentralrs587776834
openSNPrs587776834
23andMers587776834
23andMe allrs587776834
SNP Nexus

SNPshotrs587776834
SNPdbers587776834
MSV3drs587776834
GWAS Ctlgrs587776834
Max Magnitude0
ClinVar
Risk rs587776834(ATCT,T;ATCT,T)
Alt rs587776834(ATCT,T;ATCT,T)
Reference rs587776834(GATT;GATT)
Significance Pathogenic
Disease Acute lymphoid leukemia
Variation info
Gene FLT3
CLNDBN Acute lymphoid leukemia
Reversed 1
HGVS NC_000013.10:g.28608277_28608279delATC
CLNSRC OMIM Allelic Variant
CLNACC RCV000017668.5,