rs121913467

Orientation

plus

Stabilized

plus

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

Make rs121913467(A;A)

Make rs121913467(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174730

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913467
dbSNP (classic)	rs121913467
ClinGen	rs121913467
ebi	rs121913467
HLI	rs121913467
Exac	rs121913467
Gnomad	rs121913467
Varsome	rs121913467
LitVar	rs121913467
Map	rs121913467
PheGenI	rs121913467
Biobank	rs121913467
1000 genomes	rs121913467
hgdp	rs121913467
ensembl	rs121913467
geneview	rs121913467
scholar	rs121913467
google	rs121913467
pharmgkb	rs121913467
gwascentral	rs121913467
openSNP	rs121913467
23andMe	rs121913467
SNPshot	rs121913467
SNPdbe	rs121913467
MSV3d	rs121913467
GWAS Ctlg	rs121913467

Max Magnitude

0

ClinVar
Risk	rs121913467(A;A)
Alt	rs121913467(A;A)
Reference	Rs121913467(G;G)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer
Reversed	0
HGVS	NC_000007.13:g.55242423G>A
CLNSRC
CLNACC	RCV000444748.1,