rs1057519806

Orientation

minus

Stabilized

minus

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

Make rs1057519806(A;G)

Make rs1057519806(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

4110583

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs1057519806
dbSNP (classic)	rs1057519806
ClinGen	rs1057519806
ebi	rs1057519806
HLI	rs1057519806
Exac	rs1057519806
Gnomad	rs1057519806
Varsome	rs1057519806
LitVar	rs1057519806
Map	rs1057519806
PheGenI	rs1057519806
Biobank	rs1057519806
1000 genomes	rs1057519806
hgdp	rs1057519806
ensembl	rs1057519806
geneview	rs1057519806
scholar	rs1057519806
google	rs1057519806
pharmgkb	rs1057519806
gwascentral	rs1057519806
openSNP	rs1057519806
23andMe	rs1057519806
SNPshot	rs1057519806
SNPdbe	rs1057519806
MSV3d	rs1057519806
GWAS Ctlg	rs1057519806

Max Magnitude

0

ClinVar
Risk	rs1057519806(G;G)
Alt	rs1057519806(G;G)
Reference	Rs1057519806(A;A)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	MAP2K2
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000019.9:g.4110581T>C
CLNSRC
CLNACC	RCV000429584.1,