rs1057519908

Orientation

plus

Stabilized

plus

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

Make rs1057519908(G;G)

Make rs1057519908(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66435105

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs1057519908
dbSNP (classic)	rs1057519908
ClinGen	rs1057519908
ebi	rs1057519908
HLI	rs1057519908
Exac	rs1057519908
Gnomad	rs1057519908
Varsome	rs1057519908
LitVar	rs1057519908
Map	rs1057519908
PheGenI	rs1057519908
Biobank	rs1057519908
1000 genomes	rs1057519908
hgdp	rs1057519908
ensembl	rs1057519908
geneview	rs1057519908
scholar	rs1057519908
google	rs1057519908
pharmgkb	rs1057519908
gwascentral	rs1057519908
openSNP	rs1057519908
23andMe	rs1057519908
SNPshot	rs1057519908
SNPdbe	rs1057519908
MSV3d	rs1057519908
GWAS Ctlg	rs1057519908

Max Magnitude

0

ClinVar
Risk	rs1057519908(G;G)
Alt	rs1057519908(G;G)
Reference	Rs1057519908(T;T)
Significance	Probable-Pathogenic
Disease	Colorectal Neoplasms Malignant melanoma of skin Adenocarcinoma of lung Adenocarcinoma of stomach
Variation	info
Gene	MAP2K1
CLNDBN	Colorectal Neoplasms Malignant melanoma of skin Adenocarcinoma of lung Adenocarcinoma of stomach
Reversed	0
HGVS	NC_000015.9:g.66727443T>G
CLNSRC
CLNACC	RCV000419468.1, RCV000430169.1, RCV000436917.1, RCV000440832.1,