rs587780082

Orientation

minus

Stabilized

minus

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

Make rs587780082(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

45331835

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs587780082
dbSNP (classic)	rs587780082
ClinGen	rs587780082
ebi	rs587780082
HLI	rs587780082
Exac	rs587780082
Gnomad	rs587780082
Varsome	rs587780082
LitVar	rs587780082
Map	rs587780082
PheGenI	rs587780082
Biobank	rs587780082
1000 genomes	rs587780082
hgdp	rs587780082
ensembl	rs587780082
geneview	rs587780082
scholar	rs587780082
google	rs587780082
pharmgkb	rs587780082
gwascentral	rs587780082
openSNP	rs587780082
23andMe	rs587780082
SNPshot	rs587780082
SNPdbe	rs587780082
MSV3d	rs587780082
GWAS Ctlg	rs587780082

Max Magnitude

3

ClinVar
Risk	rs587780082(T;T)
Alt	rs587780082(T;T)
Reference	Rs587780082(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis
Reversed	1
HGVS	NC_000001.10:g.45797507G>A
CLNSRC
CLNACC	RCV000115753.7, RCV000212713.2, RCV000465024.1,