rs397517086

Orientation

plus

Stabilized

plus

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

Make rs397517086(-;-)

Make rs397517086(-;AAC)

Reference

GRCh38 38.1/141

Chromosome

7

Position

55173986

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs397517086
dbSNP (classic)	rs397517086
ClinGen	rs397517086
ebi	rs397517086
HLI	rs397517086
Exac	rs397517086
Gnomad	rs397517086
Varsome	rs397517086
LitVar	rs397517086
Map	rs397517086
PheGenI	rs397517086
Biobank	rs397517086
1000 genomes	rs397517086
hgdp	rs397517086
ensembl	rs397517086
geneview	rs397517086
scholar	rs397517086
google	rs397517086
pharmgkb	rs397517086
gwascentral	rs397517086
openSNP	rs397517086
23andMe	rs397517086
SNPshot	rs397517086
SNPdbe	rs397517086
MSV3d	rs397517086
GWAS Ctlg	rs397517086

Max Magnitude

0

ClinVar
Risk	rs397517086(-;-)
Alt	rs397517086(-;-)
Reference	Rs397517086(AAC;AAC)
Significance	Pathogenic
Disease	Non-small cell lung cancer
Variation	info
Gene	EGFR
CLNDBN	Non-small cell lung cancer
Reversed	0
HGVS	NC_000007.13:g.55241679_55241681delAAC
CLNSRC	COSMIC
CLNACC	RCV000038375.2,