rs1057519821

Orientation

plus

Stabilized

plus

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

Make rs1057519821(C;C)

Make rs1057519821(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66436814

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs1057519821
dbSNP (classic)	rs1057519821
ClinGen	rs1057519821
ebi	rs1057519821
HLI	rs1057519821
Exac	rs1057519821
Gnomad	rs1057519821
Varsome	rs1057519821
LitVar	rs1057519821
Map	rs1057519821
PheGenI	rs1057519821
Biobank	rs1057519821
1000 genomes	rs1057519821
hgdp	rs1057519821
ensembl	rs1057519821
geneview	rs1057519821
scholar	rs1057519821
google	rs1057519821
pharmgkb	rs1057519821
gwascentral	rs1057519821
openSNP	rs1057519821
23andMe	rs1057519821
SNPshot	rs1057519821
SNPdbe	rs1057519821
MSV3d	rs1057519821
GWAS Ctlg	rs1057519821

Max Magnitude

0

ClinVar
Risk	rs1057519821(C;C) rs1057519821(T;T)
Alt	rs1057519821(C;C) rs1057519821(T;T)
Reference	Rs1057519821(G;G)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	MAP2K1
CLNDBN	Neoplasm
Reversed	0
HGVS	NC_000015.9:g.66729152G>C; NC_000015.9:g.66729152G>T
CLNSRC
CLNACC	RCV000433785.1, RCV000439225.1,