rs121913488

Orientation

minus

Stabilized

minus

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

Make rs121913488(C;C)

Make rs121913488(C;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

28018505

Gene

FLT3

is a	snp
is	mentioned by
dbSNP	rs121913488
dbSNP (classic)	rs121913488
ClinGen	rs121913488
ebi	rs121913488
HLI	rs121913488
Exac	rs121913488
Gnomad	rs121913488
Varsome	rs121913488
LitVar	rs121913488
Map	rs121913488
PheGenI	rs121913488
Biobank	rs121913488
1000 genomes	rs121913488
hgdp	rs121913488
ensembl	rs121913488
geneview	rs121913488
scholar	rs121913488
google	rs121913488
pharmgkb	rs121913488
gwascentral	rs121913488
openSNP	rs121913488
23andMe	rs121913488
SNPshot	rs121913488
SNPdbe	rs121913488
MSV3d	rs121913488
GWAS Ctlg	rs121913488

Merged from

Rs121909647, Rs121909648, Rs121909649

Max Magnitude

0

OMIM	136351
Desc
Variant	0004
Related	also

OMIM	136351
Desc
Variant	0005
Related	also

OMIM	136351
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121913488(A;A) rs121913488(C;C) rs121913488(T;T)
Alt	rs121913488(A;A) rs121913488(C;C) rs121913488(T;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 UniProtKB (protein)
CLNACC	RCV000017665.5, RCV000017666.4, RCV000017662.6, RCV000017663.6,