rs199474826

Orientation

plus

Stabilized

plus

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

Make rs199474826(A;A)

Make rs199474826(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

8009

Gene

COX2

is a	snp
is	mentioned by
dbSNP	rs199474826
dbSNP (classic)	rs199474826
ClinGen	rs199474826
ebi	rs199474826
HLI	rs199474826
Exac	rs199474826
Gnomad	rs199474826
Varsome	rs199474826
LitVar	rs199474826
Map	rs199474826
PheGenI	rs199474826
Biobank	rs199474826
1000 genomes	rs199474826
hgdp	rs199474826
ensembl	rs199474826
geneview	rs199474826
scholar	rs199474826
google	rs199474826
pharmgkb	rs199474826
gwascentral	rs199474826
openSNP	rs199474826
23andMe	rs199474826
SNPshot	rs199474826
SNPdbe	rs199474826
MSV3d	rs199474826
GWAS Ctlg	rs199474826

Max Magnitude

0

ClinVar
Risk	rs199474826(A;A)
Alt	rs199474826(A;A)
Reference	Rs199474826(G;G)
Significance	Pathogenic
Disease	Familial colorectal cancer
Variation	info
Gene	COX2
CLNDBN	Familial colorectal cancer
Reversed	0
HGVS	NC_012920.1:m.8009G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010295.2,