rs267606882

Orientation

plus

Stabilized

plus

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

Make rs267606882(A;A)

Make rs267606882(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

6264

Gene

COX1

is a	snp
is	mentioned by
dbSNP	rs267606882
dbSNP (classic)	rs267606882
ClinGen	rs267606882
ebi	rs267606882
HLI	rs267606882
Exac	rs267606882
Gnomad	rs267606882
Varsome	rs267606882
LitVar	rs267606882
Map	rs267606882
PheGenI	rs267606882
Biobank	rs267606882
1000 genomes	rs267606882
hgdp	rs267606882
ensembl	rs267606882
geneview	rs267606882
scholar	rs267606882
google	rs267606882
pharmgkb	rs267606882
gwascentral	rs267606882
openSNP	rs267606882
23andMe	rs267606882
SNPshot	rs267606882
SNPdbe	rs267606882
MSV3d	rs267606882
GWAS Ctlg	rs267606882

Max Magnitude

0

ClinVar
Risk	rs267606882(A;A)
Alt	rs267606882(A;A)
Reference	Rs267606882(G;G)
Significance	Pathogenic
Disease	Familial colorectal cancer
Variation	info
Gene	COX1
CLNDBN	Familial colorectal cancer
Reversed	0
HGVS	NC_012920.1:m.6264G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010305.2,