rs1057518074

Orientation

plus

Stabilized

plus

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

Make rs1057518074(A;A)

Make rs1057518074(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

118478096

Gene

KMT2A

is a	snp
is	mentioned by
dbSNP	rs1057518074
dbSNP (classic)	rs1057518074
ClinGen	rs1057518074
ebi	rs1057518074
HLI	rs1057518074
Exac	rs1057518074
Gnomad	rs1057518074
Varsome	rs1057518074
LitVar	rs1057518074
Map	rs1057518074
PheGenI	rs1057518074
Biobank	rs1057518074
1000 genomes	rs1057518074
hgdp	rs1057518074
ensembl	rs1057518074
geneview	rs1057518074
scholar	rs1057518074
google	rs1057518074
pharmgkb	rs1057518074
gwascentral	rs1057518074
openSNP	rs1057518074
23andMe	rs1057518074
SNPshot	rs1057518074
SNPdbe	rs1057518074
MSV3d	rs1057518074
GWAS Ctlg	rs1057518074

Max Magnitude

0

ClinVar
Risk	rs1057518074(A;A)
Alt	rs1057518074(A;A)
Reference	Rs1057518074(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KMT2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.118348811G>A
CLNSRC
CLNACC	RCV000414422.1,