rs121913418

Orientation

plus

Stabilized

plus

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

Make rs121913418(A;A)

Make rs121913418(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174818

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913418
dbSNP (classic)	rs121913418
ClinGen	rs121913418
ebi	rs121913418
HLI	rs121913418
Exac	rs121913418
Gnomad	rs121913418
Varsome	rs121913418
LitVar	rs121913418
Map	rs121913418
PheGenI	rs121913418
Biobank	rs121913418
1000 genomes	rs121913418
hgdp	rs121913418
ensembl	rs121913418
geneview	rs121913418
scholar	rs121913418
google	rs121913418
pharmgkb	rs121913418
gwascentral	rs121913418
openSNP	rs121913418
23andMe	rs121913418
SNPshot	rs121913418
SNPdbe	rs121913418
MSV3d	rs121913418
GWAS Ctlg	rs121913418

Max Magnitude

0

ClinVar
Risk	rs121913418(A;A) rs121913418(T;T)
Alt	rs121913418(A;A) rs121913418(T;T)
Reference	Rs121913418(G;G)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer not specified
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer not specified
Reversed	0
HGVS	NC_000007.13:g.55242511G>A; NC_000007.13:g.55242511G>T
CLNSRC
CLNACC	RCV000425618.1, RCV000038400.2, RCV000435465.1,