rs876660774

Orientation

minus

Stabilized

minus

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

Make rs876660774(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

45331187

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs876660774
dbSNP (classic)	rs876660774
ClinGen	rs876660774
ebi	rs876660774
HLI	rs876660774
Exac	rs876660774
Gnomad	rs876660774
Varsome	rs876660774
LitVar	rs876660774
Map	rs876660774
PheGenI	rs876660774
Biobank	rs876660774
1000 genomes	rs876660774
hgdp	rs876660774
ensembl	rs876660774
geneview	rs876660774
scholar	rs876660774
google	rs876660774
pharmgkb	rs876660774
gwascentral	rs876660774
openSNP	rs876660774
23andMe	rs876660774
SNPshot	rs876660774
SNPdbe	rs876660774
MSV3d	rs876660774
GWAS Ctlg	rs876660774

Max Magnitude

3

ClinVar
Risk	rs876660774(T;T)
Alt	rs876660774(T;T)
Reference	Rs876660774(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000001.10:g.45796859T>A
CLNSRC
CLNACC	RCV000219128.1,