rs121913229

Orientation

plus

Stabilized

plus

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

Make rs121913229(C;C)

Make rs121913229(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174785

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913229
dbSNP (classic)	rs121913229
ClinGen	rs121913229
ebi	rs121913229
HLI	rs121913229
Exac	rs121913229
Gnomad	rs121913229
Varsome	rs121913229
LitVar	rs121913229
Map	rs121913229
PheGenI	rs121913229
Biobank	rs121913229
1000 genomes	rs121913229
hgdp	rs121913229
ensembl	rs121913229
geneview	rs121913229
scholar	rs121913229
google	rs121913229
pharmgkb	rs121913229
gwascentral	rs121913229
openSNP	rs121913229
23andMe	rs121913229
SNPshot	rs121913229
SNPdbe	rs121913229
MSV3d	rs121913229
GWAS Ctlg	rs121913229

Max Magnitude

0

ClinVar
Risk	rs121913229(C;C)
Alt	rs121913229(C;C)
Reference	Rs121913229(G;G)
Significance	Probable-Pathogenic
Disease	not specified Non-small cell lung cancer Adenocarcinoma of lung
Variation	info
Gene	EGFR
CLNDBN	not specified Non-small cell lung cancer Adenocarcinoma of lung
Reversed	0
HGVS	NC_000007.13:g.55242478G>C
CLNSRC
CLNACC	RCV000038395.2, RCV000425827.1, RCV000442888.1,