rs121913446

Orientation

plus

Stabilized

plus

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

Make rs121913446(C;T)

Make rs121913446(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174735

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913446
dbSNP (classic)	rs121913446
ClinGen	rs121913446
ebi	rs121913446
HLI	rs121913446
Exac	rs121913446
Gnomad	rs121913446
Varsome	rs121913446
LitVar	rs121913446
Map	rs121913446
PheGenI	rs121913446
Biobank	rs121913446
1000 genomes	rs121913446
hgdp	rs121913446
ensembl	rs121913446
geneview	rs121913446
scholar	rs121913446
google	rs121913446
pharmgkb	rs121913446
gwascentral	rs121913446
openSNP	rs121913446
23andMe	rs121913446
SNPshot	rs121913446
SNPdbe	rs121913446
MSV3d	rs121913446
GWAS Ctlg	rs121913446

Max Magnitude

0

ClinVar
Risk	rs121913446(T;T)
Alt	rs121913446(T;T)
Reference	Rs121913446(C;C)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer Esophageal Squamous Cell Carcinoma
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer Esophageal Squamous Cell Carcinoma
Reversed	0
HGVS	NC_000007.13:g.55242428C>T
CLNSRC
CLNACC	RCV000428149.1, RCV000441469.1,