rs121913427

Orientation

plus

Stabilized

plus

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

Make rs121913427(A;A)

Make rs121913427(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174773

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913427
dbSNP (classic)	rs121913427
ClinGen	rs121913427
ebi	rs121913427
HLI	rs121913427
Exac	rs121913427
Gnomad	rs121913427
Varsome	rs121913427
LitVar	rs121913427
Map	rs121913427
PheGenI	rs121913427
Biobank	rs121913427
1000 genomes	rs121913427
hgdp	rs121913427
ensembl	rs121913427
geneview	rs121913427
scholar	rs121913427
google	rs121913427
pharmgkb	rs121913427
gwascentral	rs121913427
openSNP	rs121913427
23andMe	rs121913427
SNPshot	rs121913427
SNPdbe	rs121913427
MSV3d	rs121913427
GWAS Ctlg	rs121913427

Max Magnitude

0

ClinVar
Risk	rs121913427(A;A) rs121913427(C;C)
Alt	rs121913427(A;A) rs121913427(C;C)
Reference	Rs121913427(G;G)
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.55242466G>A; NC_000007.13:g.55242466G>C
CLNSRC
CLNACC	RCV000424472.1, RCV000154381.1,