Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520021(C;C)
Make rs1057520021(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28034139
GeneFLT3
is asnp
is mentioned by
dbSNPrs1057520021
dbSNP (classic)rs1057520021
ClinGenrs1057520021
ebirs1057520021
HLIrs1057520021
Exacrs1057520021
Gnomadrs1057520021
Varsomers1057520021
LitVarrs1057520021
Maprs1057520021
PheGenIrs1057520021
Biobankrs1057520021
1000 genomesrs1057520021
hgdprs1057520021
ensemblrs1057520021
geneviewrs1057520021
scholarrs1057520021
googlers1057520021
pharmgkbrs1057520021
gwascentralrs1057520021
openSNPrs1057520021
23andMers1057520021
23andMe allrs1057520021
SNPshotrs1057520021
SNPdbers1057520021
MSV3drs1057520021
GWAS Ctlgrs1057520021
Max Magnitude0
ClinVar
Risk rs1057520021(C;C)
Alt rs1057520021(C;C)
Reference Rs1057520021(T;T)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28608276A>G
CLNSRC
CLNACC RCV000432251.1,