rs121913433

Orientation

plus

Stabilized

plus

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

Make rs121913433(A;G)

Make rs121913433(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

55174771

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs121913433
dbSNP (classic)	rs121913433
ClinGen	rs121913433
ebi	rs121913433
HLI	rs121913433
Exac	rs121913433
Gnomad	rs121913433
Varsome	rs121913433
LitVar	rs121913433
Map	rs121913433
PheGenI	rs121913433
Biobank	rs121913433
1000 genomes	rs121913433
hgdp	rs121913433
ensembl	rs121913433
geneview	rs121913433
scholar	rs121913433
google	rs121913433
pharmgkb	rs121913433
gwascentral	rs121913433
openSNP	rs121913433
23andMe	rs121913433
SNPshot	rs121913433
SNPdbe	rs121913433
MSV3d	rs121913433
GWAS Ctlg	rs121913433

Max Magnitude

0

ClinVar
Risk	rs121913433(G;G)
Alt	rs121913433(G;G)
Reference	Rs121913433(A;A)
Significance	Probable-Pathogenic
Disease	Squamous cell carcinoma of the head and neck
Variation	info
Gene	EGFR
CLNDBN	Squamous cell carcinoma of the head and neck
Reversed	0
HGVS	NC_000007.13:g.55242464A>G
CLNSRC
CLNACC	RCV000433245.1,