rs150800017

Orientation

plus

Stabilized

plus

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

Make rs150800017(C;G)

Make rs150800017(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

118489816

Gene

KMT2A

is a	snp
is	mentioned by
dbSNP	rs150800017
dbSNP (classic)	rs150800017
ClinGen	rs150800017
ebi	rs150800017
HLI	rs150800017
Exac	rs150800017
Gnomad	rs150800017
Varsome	rs150800017
LitVar	rs150800017
Map	rs150800017
PheGenI	rs150800017
Biobank	rs150800017
1000 genomes	rs150800017
hgdp	rs150800017
ensembl	rs150800017
geneview	rs150800017
scholar	rs150800017
google	rs150800017
pharmgkb	rs150800017
gwascentral	rs150800017
openSNP	rs150800017
23andMe	rs150800017
SNPshot	rs150800017
SNPdbe	rs150800017
MSV3d	rs150800017
GWAS Ctlg	rs150800017

Max Magnitude

0

ClinVar
Risk	rs150800017(G;G) rs150800017(T;T)
Alt	rs150800017(G;G) rs150800017(T;T)
Reference	Rs150800017(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KMT2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.118360531C>T
CLNSRC
CLNACC	RCV000429808.1,