rs1057519910

Orientation

minus

Stabilized

minus

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

Make rs1057519910(G;G)

Make rs1057519910(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

4117551

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs1057519910
dbSNP (classic)	rs1057519910
ClinGen	rs1057519910
ebi	rs1057519910
HLI	rs1057519910
Exac	rs1057519910
Gnomad	rs1057519910
Varsome	rs1057519910
LitVar	rs1057519910
Map	rs1057519910
PheGenI	rs1057519910
Biobank	rs1057519910
1000 genomes	rs1057519910
hgdp	rs1057519910
ensembl	rs1057519910
geneview	rs1057519910
scholar	rs1057519910
google	rs1057519910
pharmgkb	rs1057519910
gwascentral	rs1057519910
openSNP	rs1057519910
23andMe	rs1057519910
SNPshot	rs1057519910
SNPdbe	rs1057519910
MSV3d	rs1057519910
GWAS Ctlg	rs1057519910

Max Magnitude

0

ClinVar
Risk	rs1057519910(G;G)
Alt	rs1057519910(G;G)
Reference	Rs1057519910(T;T)
Significance	Probable-Pathogenic
Disease	Malignant melanoma of skin Pancreatic adenocarcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach
Variation	info
Gene	MAP2K2
CLNDBN	Malignant melanoma of skin Pancreatic adenocarcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach
Reversed	1
HGVS	NC_000019.9:g.4117549A>C
CLNSRC
CLNACC	RCV000417753.1, RCV000428429.1, RCV000429600.1, RCV000438529.1,