rs864309569

Orientation

plus

Stabilized

plus

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

Make rs864309569(C;G)

Make rs864309569(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

118501681

Gene

KMT2A

is a	snp
is	mentioned by
dbSNP	rs864309569
dbSNP (classic)	rs864309569
ClinGen	rs864309569
ebi	rs864309569
HLI	rs864309569
Exac	rs864309569
Gnomad	rs864309569
Varsome	rs864309569
LitVar	rs864309569
Map	rs864309569
PheGenI	rs864309569
Biobank	rs864309569
1000 genomes	rs864309569
hgdp	rs864309569
ensembl	rs864309569
geneview	rs864309569
scholar	rs864309569
google	rs864309569
pharmgkb	rs864309569
gwascentral	rs864309569
openSNP	rs864309569
23andMe	rs864309569
SNPshot	rs864309569
SNPdbe	rs864309569
MSV3d	rs864309569
GWAS Ctlg	rs864309569

Max Magnitude

0

ClinVar
Risk	rs864309569(G;G)
Alt	rs864309569(G;G)
Reference	Rs864309569(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KMT2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.118372396C>G
CLNSRC
CLNACC	RCV000203050.1,