rs121913231

Orientation

plus

Stabilized

plus

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

Make rs121913231(C;T)

Make rs121913231(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174794

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913231
dbSNP (classic)	rs121913231
ClinGen	rs121913231
ebi	rs121913231
HLI	rs121913231
Exac	rs121913231
Gnomad	rs121913231
Varsome	rs121913231
LitVar	rs121913231
Map	rs121913231
PheGenI	rs121913231
Biobank	rs121913231
1000 genomes	rs121913231
hgdp	rs121913231
ensembl	rs121913231
geneview	rs121913231
scholar	rs121913231
google	rs121913231
pharmgkb	rs121913231
gwascentral	rs121913231
openSNP	rs121913231
23andMe	rs121913231
SNPshot	rs121913231
SNPdbe	rs121913231
MSV3d	rs121913231
GWAS Ctlg	rs121913231

Max Magnitude

0

ClinVar
Risk	rs121913231(T;T)
Alt	rs121913231(T;T)
Reference	Rs121913231(C;C)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer Head and Neck Neoplasms
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer Head and Neck Neoplasms
Reversed	0
HGVS	NC_000007.13:g.55242487C>T
CLNSRC
CLNACC	RCV000436542.1, RCV000441908.1,