rs397509368

Orientation

plus

Stabilized

plus

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

Make rs397509368(C;C)

Make rs397509368(C;TTAAGAGAAGCAA)

Reference

GRCh38 38.1/141

Chromosome

7

Position

55174776

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs397509368
dbSNP (classic)	rs397509368
ClinGen	rs397509368
ebi	rs397509368
HLI	rs397509368
Exac	rs397509368
Gnomad	rs397509368
Varsome	rs397509368
LitVar	rs397509368
Map	rs397509368
PheGenI	rs397509368
Biobank	rs397509368
1000 genomes	rs397509368
hgdp	rs397509368
ensembl	rs397509368
geneview	rs397509368
scholar	rs397509368
google	rs397509368
pharmgkb	rs397509368
gwascentral	rs397509368
openSNP	rs397509368
23andMe	rs397509368
SNPshot	rs397509368
SNPdbe	rs397509368
MSV3d	rs397509368
GWAS Ctlg	rs397509368

Max Magnitude

0

ClinVar
Risk	rs397509368(C;C)
Alt	rs397509368(C;C)
Reference	Rs397509368(TTAAGAGAAGCAA;TTAAGAGAAGCAA)
Significance	Drug-response
Disease	Nonsmall cell lung cancer Tyrosine kinase inhibitor response
Variation	info
Gene	EGFR
CLNDBN	Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, somatic Tyrosine kinase inhibitor response
Reversed	0
HGVS	NC_000007.13:g.55242469_55242481delTTAAGAGAAGCAAinsC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018085.86, RCV000154240.1,