rs1057519887

Orientation

plus

Stabilized

plus

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

Make rs1057519887(AA;AA)

Make rs1057519887(AA;GC)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55154128

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs1057519887
dbSNP (classic)	rs1057519887
ClinGen	rs1057519887
ebi	rs1057519887
HLI	rs1057519887
Exac	rs1057519887
Gnomad	rs1057519887
Varsome	rs1057519887
LitVar	rs1057519887
Map	rs1057519887
PheGenI	rs1057519887
Biobank	rs1057519887
1000 genomes	rs1057519887
hgdp	rs1057519887
ensembl	rs1057519887
geneview	rs1057519887
scholar	rs1057519887
google	rs1057519887
pharmgkb	rs1057519887
gwascentral	rs1057519887
openSNP	rs1057519887
23andMe	rs1057519887
SNPshot	rs1057519887
SNPdbe	rs1057519887
MSV3d	rs1057519887
GWAS Ctlg	rs1057519887

Max Magnitude

0

ClinVar
Risk	rs1057519887(AA;AA) rs1057519887(AT;AT)
Alt	rs1057519887(AA;AA) rs1057519887(AT;AT)
Reference	Rs1057519887(GC;GC)
Significance	Probable-Pathogenic
Disease	Glioblastoma Squamous cell carcinoma of the head and neck Neoplasm of brain
Variation	info
Gene	EGFR
CLNDBN	Glioblastoma Squamous cell carcinoma of the head and neck Neoplasm of brain
Reversed	0
HGVS	NC_000007.13:g.55221821_55221822delGCinsAA; NC_000007.13:g.55221821_55221822delGCinsAT
CLNSRC
CLNACC	RCV000424975.1, RCV000437629.1, RCV000442544.1, RCV000417429.1, RCV000429429.1, RCV000435251.1,