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rs121913488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913488(C;C)
Make rs121913488(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position28018505
GeneFLT3
is asnp
is mentioned by
dbSNPrs121913488
ebirs121913488
HLIrs121913488
Exacrs121913488
Varsomers121913488
Maprs121913488
PheGenIrs121913488
hapmaprs121913488
1000 genomesrs121913488
hgdprs121913488
ensemblrs121913488
gopubmedrs121913488
geneviewrs121913488
scholarrs121913488
googlers121913488
pharmgkbrs121913488
gwascentralrs121913488
openSNPrs121913488
23andMers121913488
23andMe allrs121913488
SNP Nexus

SNPshotrs121913488
SNPdbers121913488
MSV3drs121913488
GWAS Ctlgrs121913488
Merged fromRs121909647, Rs121909648, Rs121909649
Max Magnitude0
OMIM136351
Desc
Variant0004
Relatedalso
OMIM136351
Desc
Variant0005
Relatedalso
OMIM136351
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913488(A,C,T;A,C,T)
Alt rs121913488(A,C,T;A,C,T)
Reference rs121913488(G;G)
Significance Pathogenic
Disease Acute myeloid leukemia Acute lymphoid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia Acute lymphoid leukemia
Reversed 1
HGVS NC_000013.10:g.28592642C>A; NC_000013.10:g.28592642C>G; NC_000013.10:g.28592642C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017665.4, RCV000017666.4, RCV000017662.5, RCV000017663.5,