rs121913430

Orientation

plus

Stabilized

plus

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

Make rs121913430(A;A)

Make rs121913430(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174740

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913430
dbSNP (classic)	rs121913430
ClinGen	rs121913430
ebi	rs121913430
HLI	rs121913430
Exac	rs121913430
Gnomad	rs121913430
Varsome	rs121913430
LitVar	rs121913430
Map	rs121913430
PheGenI	rs121913430
Biobank	rs121913430
1000 genomes	rs121913430
hgdp	rs121913430
ensembl	rs121913430
geneview	rs121913430
scholar	rs121913430
google	rs121913430
pharmgkb	rs121913430
gwascentral	rs121913430
openSNP	rs121913430
23andMe	rs121913430
SNPshot	rs121913430
SNPdbe	rs121913430
MSV3d	rs121913430
GWAS Ctlg	rs121913430

Max Magnitude

0

ClinVar
Risk	rs121913430(A;A)
Alt	rs121913430(A;A)
Reference	Rs121913430(G;G)
Significance	Probable-Pathogenic
Disease	Non-small cell lung cancer Prostatic Neoplasms
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer Prostatic Neoplasms
Reversed	0
HGVS	NC_000007.13:g.55242433G>A
CLNSRC
CLNACC	RCV000434054.1, RCV000442962.1,