rs587782885

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	3	Carrier of a MUTYH-related familial adenomatous polyposis mutation
(C;T)	3	Carrier of a MUTYH-related familial adenomatous polyposis mutation

Make rs587782885(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

45332440

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs587782885
dbSNP (classic)	rs587782885
ClinGen	rs587782885
ebi	rs587782885
HLI	rs587782885
Exac	rs587782885
Gnomad	rs587782885
Varsome	rs587782885
LitVar	rs587782885
Map	rs587782885
PheGenI	rs587782885
Biobank	rs587782885
1000 genomes	rs587782885
hgdp	rs587782885
ensembl	rs587782885
geneview	rs587782885
scholar	rs587782885
google	rs587782885
pharmgkb	rs587782885
gwascentral	rs587782885
openSNP	rs587782885
23andMe	rs587782885
SNPshot	rs587782885
SNPdbe	rs587782885
MSV3d	rs587782885
GWAS Ctlg	rs587782885

Max Magnitude

3

ClinVar
Risk	rs587782885(T;T)
Alt	rs587782885(T;T)
Reference	Rs587782885(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Carcinoma of colon not provided
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome Carcinoma of colon not provided
Reversed	1
HGVS	NC_000001.10:g.45798112G>A
CLNSRC
CLNACC	RCV000132522.4, RCV000144630.1, RCV000236829.1,