rs1057519807

Orientation

minus

Stabilized

minus

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

Make rs1057519807(A;A)

Make rs1057519807(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

4110586

Gene

MAP2K2

is a	snp
is	mentioned by
dbSNP	rs1057519807
dbSNP (classic)	rs1057519807
ClinGen	rs1057519807
ebi	rs1057519807
HLI	rs1057519807
Exac	rs1057519807
Gnomad	rs1057519807
Varsome	rs1057519807
LitVar	rs1057519807
Map	rs1057519807
PheGenI	rs1057519807
Biobank	rs1057519807
1000 genomes	rs1057519807
hgdp	rs1057519807
ensembl	rs1057519807
geneview	rs1057519807
scholar	rs1057519807
google	rs1057519807
pharmgkb	rs1057519807
gwascentral	rs1057519807
openSNP	rs1057519807
23andMe	rs1057519807
SNPshot	rs1057519807
SNPdbe	rs1057519807
MSV3d	rs1057519807
GWAS Ctlg	rs1057519807

Max Magnitude

0

ClinVar
Risk	rs1057519807(A;A)
Alt	rs1057519807(A;A)
Reference	Rs1057519807(T;T)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	MAP2K2
CLNDBN	Malignant melanoma
Reversed	1
HGVS	NC_000019.9:g.4110584A>T
CLNSRC
CLNACC	RCV000438500.1,