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rs398122514

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122514(-;-)
Make rs398122514(-;GGATCC)
Make rs398122514(GGATCC;GGATCC)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position28018487
GeneFLT3
is asnp
is mentioned by
dbSNPrs398122514
ebirs398122514
HLIrs398122514
Exacrs398122514
Varsomers398122514
Maprs398122514
PheGenIrs398122514
hapmaprs398122514
1000 genomesrs398122514
hgdprs398122514
ensemblrs398122514
gopubmedrs398122514
geneviewrs398122514
scholarrs398122514
googlers398122514
pharmgkbrs398122514
gwascentralrs398122514
openSNPrs398122514
23andMers398122514
23andMe allrs398122514
SNP Nexus

SNPshotrs398122514
SNPdbers398122514
MSV3drs398122514
GWAS Ctlgrs398122514
Max Magnitude0
ClinVar
Risk rs398122514(GGATCC;GGATCC)
Alt rs398122514(GGATCC;GGATCC)
Reference rs398122514(;)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene FLT3
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000013.10:g.28592624_28592625insGGATCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000017659.4,