rs1057519810

Orientation

minus

Stabilized

minus

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

Make rs1057519810(A;A)

Make rs1057519810(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

4117619

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs1057519810
dbSNP (classic)	rs1057519810
ClinGen	rs1057519810
ebi	rs1057519810
HLI	rs1057519810
Exac	rs1057519810
Gnomad	rs1057519810
Varsome	rs1057519810
LitVar	rs1057519810
Map	rs1057519810
PheGenI	rs1057519810
Biobank	rs1057519810
1000 genomes	rs1057519810
hgdp	rs1057519810
ensembl	rs1057519810
geneview	rs1057519810
scholar	rs1057519810
google	rs1057519810
pharmgkb	rs1057519810
gwascentral	rs1057519810
openSNP	rs1057519810
23andMe	rs1057519810
SNPshot	rs1057519810
SNPdbe	rs1057519810
MSV3d	rs1057519810
GWAS Ctlg	rs1057519810

Max Magnitude

0

ClinVar
Risk	rs1057519810(A;A)
Alt	rs1057519810(A;A)
Reference	Rs1057519810(G;G)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	MAP2K2
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000019.9:g.4117617C>T
CLNSRC
CLNACC	RCV000444084.1,