rs730880502

Orientation

plus

Stabilized

plus

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

Make rs730880502(G;G)

Make rs730880502(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

66436762

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs730880502
dbSNP (classic)	rs730880502
ClinGen	rs730880502
ebi	rs730880502
HLI	rs730880502
Exac	rs730880502
Gnomad	rs730880502
Varsome	rs730880502
LitVar	rs730880502
Map	rs730880502
PheGenI	rs730880502
Biobank	rs730880502
1000 genomes	rs730880502
hgdp	rs730880502
ensembl	rs730880502
geneview	rs730880502
scholar	rs730880502
google	rs730880502
pharmgkb	rs730880502
gwascentral	rs730880502
openSNP	rs730880502
23andMe	rs730880502
SNPshot	rs730880502
SNPdbe	rs730880502
MSV3d	rs730880502
GWAS Ctlg	rs730880502

Max Magnitude

0

ClinVar
Risk	rs730880502(A;A) rs730880502(G;G)
Alt	rs730880502(A;A) rs730880502(G;G)
Reference	Rs730880502(T;T)
Significance	Probable-Pathogenic
Disease	Neoplasm not specified
Variation	info
Gene	MAP2K1
CLNDBN	Neoplasm not specified
Reversed	0
HGVS	NC_000015.9:g.66729100T>A; NC_000015.9:g.66729100T>G
CLNSRC
CLNACC	RCV000429680.1, RCV000158006.1,