rs397517085

Orientation

plus

Stabilized

plus

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

Make rs397517085(A;C)

Make rs397517085(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

55173985

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs397517085
dbSNP (classic)	rs397517085
ClinGen	rs397517085
ebi	rs397517085
HLI	rs397517085
Exac	rs397517085
Gnomad	rs397517085
Varsome	rs397517085
LitVar	rs397517085
Map	rs397517085
PheGenI	rs397517085
Biobank	rs397517085
1000 genomes	rs397517085
hgdp	rs397517085
ensembl	rs397517085
geneview	rs397517085
scholar	rs397517085
google	rs397517085
pharmgkb	rs397517085
gwascentral	rs397517085
openSNP	rs397517085
23andMe	rs397517085
SNPshot	rs397517085
SNPdbe	rs397517085
MSV3d	rs397517085
GWAS Ctlg	rs397517085

Max Magnitude

0

ClinVar
Risk	rs397517085(C;C) rs397517085(G;G) rs397517085(T;T)
Alt	rs397517085(C;C) rs397517085(G;G) rs397517085(T;T)
Reference	Rs397517085(A;A)
Significance	Drug-response
Disease	not specified Lung cancer Tyrosine kinase inhibitor response
Variation	info
Gene	EGFR
CLNDBN	not specified Lung cancer Tyrosine kinase inhibitor response
Reversed	0
HGVS	NC_000007.13:g.55241678A>C; NC_000007.13:g.55241678A>G; NC_000007.13:g.55241678A>T
CLNSRC	UniProtKB (protein) UniProtKB (variants)
CLNACC	RCV000038374.2, RCV000206908.1, RCV000150615.1, RCV000207006.1, RCV000154197.1,