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rs121913232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913232(C;G)
Make rs121913232(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position28018500
GeneFLT3
is asnp
is mentioned by
dbSNPrs121913232
dbSNP (old)rs121913232
ClinGenrs121913232
ebirs121913232
HLIrs121913232
Exacrs121913232
Gnomadrs121913232
Varsomers121913232
Maprs121913232
PheGenIrs121913232
Biobankrs121913232
1000 genomesrs121913232
hgdprs121913232
ensemblrs121913232
gopubmedrs121913232
geneviewrs121913232
scholarrs121913232
googlers121913232
pharmgkbrs121913232
gwascentralrs121913232
openSNPrs121913232
23andMers121913232
23andMe allrs121913232
SNPshotrs121913232
SNPdbers121913232
MSV3drs121913232
GWAS Ctlgrs121913232
Max Magnitude0
ClinVar
Risk rs121913232(G;G)
Alt rs121913232(G;G)
Reference Rs121913232(C;C)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592637G>C
CLNSRC
CLNACC RCV000422249.1,