rs376561094

Orientation

plus

Stabilized

plus

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

Make rs376561094(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

45332636

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs376561094
dbSNP (classic)	rs376561094
ClinGen	rs376561094
ebi	rs376561094
HLI	rs376561094
Exac	rs376561094
Gnomad	rs376561094
Varsome	rs376561094
LitVar	rs376561094
Map	rs376561094
PheGenI	rs376561094
Biobank	rs376561094
1000 genomes	rs376561094
hgdp	rs376561094
ensembl	rs376561094
geneview	rs376561094
scholar	rs376561094
google	rs376561094
pharmgkb	rs376561094
gwascentral	rs376561094
openSNP	rs376561094
23andMe	rs376561094
SNPshot	rs376561094
SNPdbe	rs376561094
MSV3d	rs376561094
GWAS Ctlg	rs376561094

Max Magnitude

3

ClinVar
Risk	rs376561094(A;A)
Alt	rs376561094(A;A)
Reference	Rs376561094(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000001.10:g.45798308G>A
CLNSRC
CLNACC	RCV000223123.1, RCV000426595.1,