rs1057520667

Orientation

minus

Stabilized

minus

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

Make rs1057520667(A;A)

Make rs1057520667(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

49021873

Gene

KMT2D

is a	snp
is	mentioned by
dbSNP	rs1057520667
dbSNP (classic)	rs1057520667
ClinGen	rs1057520667
ebi	rs1057520667
HLI	rs1057520667
Exac	rs1057520667
Gnomad	rs1057520667
Varsome	rs1057520667
LitVar	rs1057520667
Map	rs1057520667
PheGenI	rs1057520667
Biobank	rs1057520667
1000 genomes	rs1057520667
hgdp	rs1057520667
ensembl	rs1057520667
geneview	rs1057520667
scholar	rs1057520667
google	rs1057520667
pharmgkb	rs1057520667
gwascentral	rs1057520667
openSNP	rs1057520667
23andMe	rs1057520667
SNPshot	rs1057520667
SNPdbe	rs1057520667
MSV3d	rs1057520667
GWAS Ctlg	rs1057520667

Max Magnitude

0

ClinVar
Risk	rs1057520667(A;A)
Alt	rs1057520667(A;A)
Reference	Rs1057520667(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KMT2D
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.49415656C>T
CLNSRC
CLNACC	RCV000428424.1,