rs121913464

Orientation

plus

Stabilized

plus

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

Make rs121913464(A;A)

Make rs121913464(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174792

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913464
dbSNP (classic)	rs121913464
ClinGen	rs121913464
ebi	rs121913464
HLI	rs121913464
Exac	rs121913464
Gnomad	rs121913464
Varsome	rs121913464
LitVar	rs121913464
Map	rs121913464
PheGenI	rs121913464
Biobank	rs121913464
1000 genomes	rs121913464
hgdp	rs121913464
ensembl	rs121913464
geneview	rs121913464
scholar	rs121913464
google	rs121913464
pharmgkb	rs121913464
gwascentral	rs121913464
openSNP	rs121913464
23andMe	rs121913464
SNPshot	rs121913464
SNPdbe	rs121913464
MSV3d	rs121913464
GWAS Ctlg	rs121913464

Max Magnitude

0

ClinVar
Risk	rs121913464(A;A)
Alt	rs121913464(A;A)
Reference	Rs121913464(C;C)
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.55242485C>A
CLNSRC
CLNACC	RCV000432149.1,