rs121909646

Orientation

minus

Stabilized

minus

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

Make rs121909646(A;T)

Make rs121909646(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

28018504

Gene

FLT3

is a	snp
is	mentioned by
dbSNP	rs121909646
dbSNP (classic)	rs121909646
ClinGen	rs121909646
ebi	rs121909646
HLI	rs121909646
Exac	rs121909646
Gnomad	rs121909646
Varsome	rs121909646
LitVar	rs121909646
Map	rs121909646
PheGenI	rs121909646
Biobank	rs121909646
1000 genomes	rs121909646
hgdp	rs121909646
ensembl	rs121909646
geneview	rs121909646
scholar	rs121909646
google	rs121909646
pharmgkb	rs121909646
gwascentral	rs121909646
openSNP	rs121909646
23andMe	rs121909646
SNPshot	rs121909646
SNPdbe	rs121909646
MSV3d	rs121909646
GWAS Ctlg	rs121909646

Max Magnitude

0

OMIM	136351
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909646(C;C) rs121909646(T;T)
Alt	rs121909646(C;C) rs121909646(T;T)
Reference	Rs121909646(A;A)
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.28592641T>A; NC_000013.10:g.28592641T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017660.6, RCV000017661.5, RCV000444069.1,