rs121913428

Orientation

plus

Stabilized

plus

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

Make rs121913428(C;C)

Make rs121913428(C;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

55174015

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913428
dbSNP (classic)	rs121913428
ClinGen	rs121913428
ebi	rs121913428
HLI	rs121913428
Exac	rs121913428
Gnomad	rs121913428
Varsome	rs121913428
LitVar	rs121913428
Map	rs121913428
PheGenI	rs121913428
Biobank	rs121913428
1000 genomes	rs121913428
hgdp	rs121913428
ensembl	rs121913428
geneview	rs121913428
scholar	rs121913428
google	rs121913428
pharmgkb	rs121913428
gwascentral	rs121913428
openSNP	rs121913428
23andMe	rs121913428
SNPshot	rs121913428
SNPdbe	rs121913428
MSV3d	rs121913428
GWAS Ctlg	rs121913428

Max Magnitude

0

ClinVar
Risk	rs121913428(A;A) rs121913428(C;C)
Alt	rs121913428(A;A) rs121913428(C;C)
Reference	Rs121913428(G;G)
Significance	Pathogenic
Disease	Non-small cell lung cancer Squamous cell carcinoma of lung Glioblastoma Adenocarcinoma of lung
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer Squamous cell carcinoma of lung Glioblastoma Adenocarcinoma of lung
Reversed	0
HGVS	NC_000007.13:g.55241708G>A; NC_000007.13:g.55241708G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000418583.1, RCV000420993.1, RCV000428419.1, RCV000439067.1, RCV000038381.3, RCV000426037.1, RCV000436293.1,