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

rs121913491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913491(A;G)
Make rs121913491(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28034204
GeneFLT3
is asnp
is mentioned by
dbSNPrs121913491
dbSNP (classic)rs121913491
ClinGenrs121913491
ebirs121913491
HLIrs121913491
Exacrs121913491
Gnomadrs121913491
Varsomers121913491
LitVarrs121913491
Maprs121913491
PheGenIrs121913491
Biobankrs121913491
1000 genomesrs121913491
hgdprs121913491
ensemblrs121913491
geneviewrs121913491
scholarrs121913491
googlers121913491
pharmgkbrs121913491
gwascentralrs121913491
openSNPrs121913491
23andMers121913491
23andMe allrs121913491
SNPshotrs121913491
SNPdbers121913491
MSV3drs121913491
GWAS Ctlgrs121913491
Max Magnitude0
ClinVar
Risk rs121913491(G;G)
Alt rs121913491(G;G)
Reference Rs121913491(A;A)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28608341T>C
CLNSRC
CLNACC RCV000444818.1,