rs1057520177

Orientation

plus

Stabilized

plus

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

Make rs1057520177(-;A)

Make rs1057520177(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

118503551

Gene

KMT2A

is a	snp
is	mentioned by
dbSNP	rs1057520177
dbSNP (classic)	rs1057520177
ClinGen	rs1057520177
ebi	rs1057520177
HLI	rs1057520177
Exac	rs1057520177
Gnomad	rs1057520177
Varsome	rs1057520177
LitVar	rs1057520177
Map	rs1057520177
PheGenI	rs1057520177
Biobank	rs1057520177
1000 genomes	rs1057520177
hgdp	rs1057520177
ensembl	rs1057520177
geneview	rs1057520177
scholar	rs1057520177
google	rs1057520177
pharmgkb	rs1057520177
gwascentral	rs1057520177
openSNP	rs1057520177
23andMe	rs1057520177
SNPshot	rs1057520177
SNPdbe	rs1057520177
MSV3d	rs1057520177
GWAS Ctlg	rs1057520177

Max Magnitude

0

ClinVar
Risk	rs1057520177(A;A)
Alt	rs1057520177(A;A)
Reference	Rs1057520177(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KMT2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.118374266dupA
CLNSRC
CLNACC	RCV000442553.1,