rs886037891

Orientation

plus

Stabilized

plus

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

Make rs886037891(G;T)

Make rs886037891(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

55155917

Gene

EGFR

is a	snp
is	mentioned by
dbSNP	rs886037891
dbSNP (classic)	rs886037891
ClinGen	rs886037891
ebi	rs886037891
HLI	rs886037891
Exac	rs886037891
Gnomad	rs886037891
Varsome	rs886037891
LitVar	rs886037891
Map	rs886037891
PheGenI	rs886037891
Biobank	rs886037891
1000 genomes	rs886037891
hgdp	rs886037891
ensembl	rs886037891
geneview	rs886037891
scholar	rs886037891
google	rs886037891
pharmgkb	rs886037891
gwascentral	rs886037891
openSNP	rs886037891
23andMe	rs886037891
SNPshot	rs886037891
SNPdbe	rs886037891
MSV3d	rs886037891
GWAS Ctlg	rs886037891

Max Magnitude

0

ClinVar
Risk	rs886037891(T;T)
Alt	rs886037891(T;T)
Reference	Rs886037891(G;G)
Significance	Pathogenic
Disease	Cowden syndrome 1
Variation	info
Gene	EGFR
CLNDBN	Cowden syndrome 1
Reversed	0
HGVS	NC_000007.13:g.55223610G>T
CLNSRC
CLNACC	RCV000256393.1,