rs1057519808

Orientation

minus

Stabilized

minus

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

Make rs1057519808(A;C)

Make rs1057519808(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

4117543

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs1057519808
dbSNP (classic)	rs1057519808
ClinGen	rs1057519808
ebi	rs1057519808
HLI	rs1057519808
Exac	rs1057519808
Gnomad	rs1057519808
Varsome	rs1057519808
LitVar	rs1057519808
Map	rs1057519808
PheGenI	rs1057519808
Biobank	rs1057519808
1000 genomes	rs1057519808
hgdp	rs1057519808
ensembl	rs1057519808
geneview	rs1057519808
scholar	rs1057519808
google	rs1057519808
pharmgkb	rs1057519808
gwascentral	rs1057519808
openSNP	rs1057519808
23andMe	rs1057519808
SNPshot	rs1057519808
SNPdbe	rs1057519808
MSV3d	rs1057519808
GWAS Ctlg	rs1057519808

Max Magnitude

0

ClinVar
Risk	rs1057519808(C;C)
Alt	rs1057519808(C;C)
Reference	Rs1057519808(A;A)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	MAP2K2
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000019.9:g.4117541T>G
CLNSRC
CLNACC	RCV000421323.1,