rs1057519888

Orientation

plus

Stabilized

plus

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

Make rs1057519888(A;G)

Make rs1057519888(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55143386

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs1057519888
dbSNP (classic)	rs1057519888
ClinGen	rs1057519888
ebi	rs1057519888
HLI	rs1057519888
Exac	rs1057519888
Gnomad	rs1057519888
Varsome	rs1057519888
LitVar	rs1057519888
Map	rs1057519888
PheGenI	rs1057519888
Biobank	rs1057519888
1000 genomes	rs1057519888
hgdp	rs1057519888
ensembl	rs1057519888
geneview	rs1057519888
scholar	rs1057519888
google	rs1057519888
pharmgkb	rs1057519888
gwascentral	rs1057519888
openSNP	rs1057519888
23andMe	rs1057519888
SNPshot	rs1057519888
SNPdbe	rs1057519888
MSV3d	rs1057519888
GWAS Ctlg	rs1057519888

Max Magnitude

0

ClinVar
Risk	rs1057519888(G;G)
Alt	rs1057519888(G;G)
Reference	Rs1057519888(A;A)
Significance	Probable-Pathogenic
Disease	Glioblastoma Neoplasm of brain Brainstem glioma
Variation	info
Gene	EGFR
CLNDBN	Glioblastoma Neoplasm of brain Brainstem glioma
Reversed	0
HGVS	NC_000007.13:g.55211079A>G
CLNSRC
CLNACC	RCV000424206.1, RCV000434481.1, RCV000440142.1,