rs1057522023

Orientation

minus

Stabilized

minus

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

Make rs1057522023(C;T)

Make rs1057522023(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

152148810

Gene

KMT2C

is a	snp
is	mentioned by
dbSNP	rs1057522023
dbSNP (classic)	rs1057522023
ClinGen	rs1057522023
ebi	rs1057522023
HLI	rs1057522023
Exac	rs1057522023
Gnomad	rs1057522023
Varsome	rs1057522023
LitVar	rs1057522023
Map	rs1057522023
PheGenI	rs1057522023
Biobank	rs1057522023
1000 genomes	rs1057522023
hgdp	rs1057522023
ensembl	rs1057522023
geneview	rs1057522023
scholar	rs1057522023
google	rs1057522023
pharmgkb	rs1057522023
gwascentral	rs1057522023
openSNP	rs1057522023
23andMe	rs1057522023
SNPshot	rs1057522023
SNPdbe	rs1057522023
MSV3d	rs1057522023
GWAS Ctlg	rs1057522023

Max Magnitude

0

ClinVar
Risk	rs1057522023(T;T)
Alt	rs1057522023(T;T)
Reference	Rs1057522023(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KMT2C
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.151845895G>A
CLNSRC
CLNACC	RCV000419858.1,