rs869025608

Orientation

plus

Stabilized

plus

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

Make rs869025608(G;T)

Make rs869025608(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

66435117

Gene

MAP2K1

is a	snp
is	mentioned by
dbSNP	rs869025608
dbSNP (classic)	rs869025608
ClinGen	rs869025608
ebi	rs869025608
HLI	rs869025608
Exac	rs869025608
Gnomad	rs869025608
Varsome	rs869025608
LitVar	rs869025608
Map	rs869025608
PheGenI	rs869025608
Biobank	rs869025608
1000 genomes	rs869025608
hgdp	rs869025608
ensembl	rs869025608
geneview	rs869025608
scholar	rs869025608
google	rs869025608
pharmgkb	rs869025608
gwascentral	rs869025608
openSNP	rs869025608
23andMe	rs869025608
SNPshot	rs869025608
SNPdbe	rs869025608
MSV3d	rs869025608
GWAS Ctlg	rs869025608

Max Magnitude

0

ClinVar
Risk	rs869025608(C;C) rs869025608(T;T)
Alt	rs869025608(C;C) rs869025608(T;T)
Reference	Rs869025608(G;G)
Significance	Pathogenic
Disease	Malignant melanoma of skin Malignant lymphoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Malignant melanoma Adenocarcinoma of prostate Adenocarcinoma of lung Cardio-facio-cutaneous syndrome Non-small cell lung cancer
Variation	info
Gene	MAP2K1
CLNDBN	Malignant melanoma of skin Malignant lymphoma, non-Hodgkin Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Malignant melanoma Adenocarcinoma of prostate Adenocarcinoma of lung Cardio-facio-cutaneous syndrome Non-small cell lung cancer
Reversed	0
HGVS	NC_000015.9:g.66727455G>C; NC_000015.9:g.66727455G>T
CLNSRC
CLNACC	RCV000419591.1, RCV000420720.1, RCV000427279.1, RCV000429649.1, RCV000430292.1, RCV000436816.1, RCV000437917.1, RCV000208748.1, RCV000421288.1, RCV000428485.1, RCV000438528.1,