rs121913466

Orientation

plus

Stabilized

plus

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

Make rs121913466(C;C)

Make rs121913466(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174762

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913466
dbSNP (classic)	rs121913466
ClinGen	rs121913466
ebi	rs121913466
HLI	rs121913466
Exac	rs121913466
Gnomad	rs121913466
Varsome	rs121913466
LitVar	rs121913466
Map	rs121913466
PheGenI	rs121913466
Biobank	rs121913466
1000 genomes	rs121913466
hgdp	rs121913466
ensembl	rs121913466
geneview	rs121913466
scholar	rs121913466
google	rs121913466
pharmgkb	rs121913466
gwascentral	rs121913466
openSNP	rs121913466
23andMe	rs121913466
SNPshot	rs121913466
SNPdbe	rs121913466
MSV3d	rs121913466
GWAS Ctlg	rs121913466

Max Magnitude

0

ClinVar
Risk	rs121913466(C;C)
Alt	rs121913466(C;C)
Reference	Rs121913466(T;T)
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.55242455T>C
CLNSRC
CLNACC	RCV000423407.1,