rs121913490

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CAT;CAT)	0	common in clinvar

Make rs121913490(-;-)

Make rs121913490(-;ATC)

Make rs121913490(ATC;ATC)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

28018500

Gene

FLT3

is a	snp
is	mentioned by
dbSNP	rs121913490
dbSNP (classic)	rs121913490
ClinGen	rs121913490
ebi	rs121913490
HLI	rs121913490
Exac	rs121913490
Gnomad	rs121913490
Varsome	rs121913490
LitVar	rs121913490
Map	rs121913490
PheGenI	rs121913490
Biobank	rs121913490
1000 genomes	rs121913490
hgdp	rs121913490
ensembl	rs121913490
geneview	rs121913490
scholar	rs121913490
google	rs121913490
pharmgkb	rs121913490
gwascentral	rs121913490
openSNP	rs121913490
23andMe	rs121913490
SNPshot	rs121913490
SNPdbe	rs121913490
MSV3d	rs121913490
GWAS Ctlg	rs121913490

Max Magnitude

0

ClinVar
Risk	rs121913490(-;-)
Alt	rs121913490(-;-)
Reference	Rs121913490(CAT;CAT)
Significance	Probable-Pathogenic
Disease	Acute myeloid leukemia
Variation	info
Gene	FLT3
CLNDBN	Acute myeloid leukemia
Reversed	1
HGVS	NC_000013.10:g.28592637_28592639delGAT
CLNSRC
CLNACC	RCV000424567.1,