rs146795390

Orientation

plus

Stabilized

plus

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

Make rs146795390(A;A)

Make rs146795390(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55191776

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs146795390
dbSNP (classic)	rs146795390
ClinGen	rs146795390
ebi	rs146795390
HLI	rs146795390
Exac	rs146795390
Gnomad	rs146795390
Varsome	rs146795390
LitVar	rs146795390
Map	rs146795390
PheGenI	rs146795390
Biobank	rs146795390
1000 genomes	rs146795390
hgdp	rs146795390
ensembl	rs146795390
geneview	rs146795390
scholar	rs146795390
google	rs146795390
pharmgkb	rs146795390
gwascentral	rs146795390
openSNP	rs146795390
23andMe	rs146795390
SNPshot	rs146795390
SNPdbe	rs146795390
MSV3d	rs146795390
GWAS Ctlg	rs146795390

Max Magnitude

0

ClinVar
Risk	rs146795390(A;A)
Alt	rs146795390(A;A)
Reference	Rs146795390(G;G)
Significance	Probable-Pathogenic
Disease	Head and Neck Neoplasms
Variation	info
Gene	EGFR
CLNDBN	Head and Neck Neoplasms
Reversed	0
HGVS	NC_000007.13:g.55259469G>A
CLNSRC
CLNACC	RCV000426205.1,