rs121913443

Orientation

plus

Stabilized

plus

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

Make rs121913443(A;A)

Make rs121913443(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55191821

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913443
dbSNP (classic)	rs121913443
ClinGen	rs121913443
ebi	rs121913443
HLI	rs121913443
Exac	rs121913443
Gnomad	rs121913443
Varsome	rs121913443
LitVar	rs121913443
Map	rs121913443
PheGenI	rs121913443
Biobank	rs121913443
1000 genomes	rs121913443
hgdp	rs121913443
ensembl	rs121913443
geneview	rs121913443
scholar	rs121913443
google	rs121913443
pharmgkb	rs121913443
gwascentral	rs121913443
openSNP	rs121913443
23andMe	rs121913443
SNPshot	rs121913443
SNPdbe	rs121913443
MSV3d	rs121913443
GWAS Ctlg	rs121913443

Max Magnitude

0

ClinVar
Risk	rs121913443(A;A) rs121913443(T;T)
Alt	rs121913443(A;A) rs121913443(T;T)
Reference	Rs121913443(C;C)
Significance	Probable-Pathogenic
Disease	not specified Non-small cell lung cancer
Variation	info
Gene	EGFR
CLNDBN	not specified Non-small cell lung cancer
Reversed	0
HGVS	NC_000007.13:g.55259514C>A; NC_000007.13:g.55259514C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000038439.2, RCV000431153.1, RCV000038440.2,