rs1057519728

Orientation

plus

Stabilized

plus

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

Make rs1057519728(C;C)

Make rs1057519728(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66435103

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs1057519728
dbSNP (classic)	rs1057519728
ClinGen	rs1057519728
ebi	rs1057519728
HLI	rs1057519728
Exac	rs1057519728
Gnomad	rs1057519728
Varsome	rs1057519728
LitVar	rs1057519728
Map	rs1057519728
PheGenI	rs1057519728
Biobank	rs1057519728
1000 genomes	rs1057519728
hgdp	rs1057519728
ensembl	rs1057519728
geneview	rs1057519728
scholar	rs1057519728
google	rs1057519728
pharmgkb	rs1057519728
gwascentral	rs1057519728
openSNP	rs1057519728
23andMe	rs1057519728
SNPshot	rs1057519728
SNPdbe	rs1057519728
MSV3d	rs1057519728
GWAS Ctlg	rs1057519728

Max Magnitude

0

ClinVar
Risk	rs1057519728(A;A) rs1057519728(C;C) rs1057519728(G;G)
Alt	rs1057519728(A;A) rs1057519728(C;C) rs1057519728(G;G)
Reference	Rs1057519728(T;T)
Significance	Pathogenic
Disease	Colorectal Neoplasms Adenocarcinoma of lung Adenocarcinoma of stomach Malignant melanoma of skin Malignant melanoma
Variation	info
Gene	MAP2K1
CLNDBN	Colorectal Neoplasms Adenocarcinoma of lung Adenocarcinoma of stomach Malignant melanoma of skin Malignant melanoma
Reversed	0
HGVS	NC_000015.9:g.66727441T>A; NC_000015.9:g.66727441T>C; NC_000015.9:g.66727441T>G
CLNSRC
CLNACC	RCV000421374.1, RCV000431446.1, RCV000432046.1, RCV000442281.1, RCV000435966.1, RCV000421852.1, RCV000422476.1, RCV000429056.1, RCV000439716.1,