rs1057519732

Orientation

plus

Stabilized

plus

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

Make rs1057519732(C;T)

Make rs1057519732(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66436824

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs1057519732
dbSNP (classic)	rs1057519732
ClinGen	rs1057519732
ebi	rs1057519732
HLI	rs1057519732
Exac	rs1057519732
Gnomad	rs1057519732
Varsome	rs1057519732
LitVar	rs1057519732
Map	rs1057519732
PheGenI	rs1057519732
Biobank	rs1057519732
1000 genomes	rs1057519732
hgdp	rs1057519732
ensembl	rs1057519732
geneview	rs1057519732
scholar	rs1057519732
google	rs1057519732
pharmgkb	rs1057519732
gwascentral	rs1057519732
openSNP	rs1057519732
23andMe	rs1057519732
SNPshot	rs1057519732
SNPdbe	rs1057519732
MSV3d	rs1057519732
GWAS Ctlg	rs1057519732

Max Magnitude

0

ClinVar
Risk	rs1057519732(T;T)
Alt	rs1057519732(T;T)
Reference	Rs1057519732(C;C)
Significance	Pathogenic
Disease	Transitional cell carcinoma of the bladder Malignant melanoma Malignant neoplasm of body of uterus Malignant melanoma of skin Colorectal Neoplasms not provided
Variation	info
Gene	MAP2K1
CLNDBN	Transitional cell carcinoma of the bladder Malignant melanoma Malignant neoplasm of body of uterus Malignant melanoma of skin Colorectal Neoplasms not provided
Reversed	0
HGVS	NC_000015.9:g.66729162C>T
CLNSRC
CLNACC	RCV000426713.1, RCV000433235.1, RCV000433927.1, RCV000443916.1, RCV000444865.1, RCV000482718.1,