rs1057519805

Orientation

plus

Stabilized

plus

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

Make rs1057519805(C;C)

Make rs1057519805(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66436839

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs1057519805
dbSNP (classic)	rs1057519805
ClinGen	rs1057519805
ebi	rs1057519805
HLI	rs1057519805
Exac	rs1057519805
Gnomad	rs1057519805
Varsome	rs1057519805
LitVar	rs1057519805
Map	rs1057519805
PheGenI	rs1057519805
Biobank	rs1057519805
1000 genomes	rs1057519805
hgdp	rs1057519805
ensembl	rs1057519805
geneview	rs1057519805
scholar	rs1057519805
google	rs1057519805
pharmgkb	rs1057519805
gwascentral	rs1057519805
openSNP	rs1057519805
23andMe	rs1057519805
SNPshot	rs1057519805
SNPdbe	rs1057519805
MSV3d	rs1057519805
GWAS Ctlg	rs1057519805

Max Magnitude

0

ClinVar
Risk	rs1057519805(C;C)
Alt	rs1057519805(C;C)
Reference	Rs1057519805(T;T)
Significance	Probable-Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	MAP2K1
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000015.9:g.66729177T>C
CLNSRC
CLNACC	RCV000422377.1,