rs1057519760

Orientation

plus

Stabilized

plus

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

Make rs1057519760(A;G)

Make rs1057519760(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55160314

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs1057519760
dbSNP (classic)	rs1057519760
ClinGen	rs1057519760
ebi	rs1057519760
HLI	rs1057519760
Exac	rs1057519760
Gnomad	rs1057519760
Varsome	rs1057519760
LitVar	rs1057519760
Map	rs1057519760
PheGenI	rs1057519760
Biobank	rs1057519760
1000 genomes	rs1057519760
hgdp	rs1057519760
ensembl	rs1057519760
geneview	rs1057519760
scholar	rs1057519760
google	rs1057519760
pharmgkb	rs1057519760
gwascentral	rs1057519760
openSNP	rs1057519760
23andMe	rs1057519760
SNPshot	rs1057519760
SNPdbe	rs1057519760
MSV3d	rs1057519760
GWAS Ctlg	rs1057519760

Max Magnitude

0

ClinVar
Risk	rs1057519760(G;G)
Alt	rs1057519760(G;G)
Reference	Rs1057519760(A;A)
Significance	Probable-Pathogenic
Disease	Colorectal Neoplasms
Variation	info
Gene	EGFR
CLNDBN	Colorectal Neoplasms
Reversed	0
HGVS	NC_000007.13:g.55228007A>G
CLNSRC
CLNACC	RCV000429440.1,