rs1057519809

Orientation

minus

Stabilized

minus

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

Make rs1057519809(C;T)

Make rs1057519809(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

4117586

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs1057519809
dbSNP (classic)	rs1057519809
ClinGen	rs1057519809
ebi	rs1057519809
HLI	rs1057519809
Exac	rs1057519809
Gnomad	rs1057519809
Varsome	rs1057519809
LitVar	rs1057519809
Map	rs1057519809
PheGenI	rs1057519809
Biobank	rs1057519809
1000 genomes	rs1057519809
hgdp	rs1057519809
ensembl	rs1057519809
geneview	rs1057519809
scholar	rs1057519809
google	rs1057519809
pharmgkb	rs1057519809
gwascentral	rs1057519809
openSNP	rs1057519809
23andMe	rs1057519809
SNPshot	rs1057519809
SNPdbe	rs1057519809
MSV3d	rs1057519809
GWAS Ctlg	rs1057519809

Max Magnitude

0

ClinVar
Risk	rs1057519809(T;T)
Alt	rs1057519809(T;T)
Reference	Rs1057519809(C;C)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	MAP2K2
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000019.9:g.4117584G>A
CLNSRC
CLNACC	RCV000432005.1,