rs1057520037

Orientation

plus

Stabilized

plus

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

Make rs1057520037(C;C)

Make rs1057520037(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174782

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs1057520037
dbSNP (classic)	rs1057520037
ClinGen	rs1057520037
ebi	rs1057520037
HLI	rs1057520037
Exac	rs1057520037
Gnomad	rs1057520037
Varsome	rs1057520037
LitVar	rs1057520037
Map	rs1057520037
PheGenI	rs1057520037
Biobank	rs1057520037
1000 genomes	rs1057520037
hgdp	rs1057520037
ensembl	rs1057520037
geneview	rs1057520037
scholar	rs1057520037
google	rs1057520037
pharmgkb	rs1057520037
gwascentral	rs1057520037
openSNP	rs1057520037
23andMe	rs1057520037
SNPshot	rs1057520037
SNPdbe	rs1057520037
MSV3d	rs1057520037
GWAS Ctlg	rs1057520037

Max Magnitude

0

ClinVar
Risk	rs1057520037(C;C)
Alt	rs1057520037(C;C)
Reference	Rs1057520037(G;G)
Significance	Probable-Pathogenic
Disease	Lung cancer
Variation	info
Gene	EGFR
CLNDBN	Lung cancer
Reversed	0
HGVS	NC_000007.13:g.55242475G>C
CLNSRC
CLNACC	RCV000444877.1,