rs121908381

Orientation

minus

Stabilized

minus

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

Make rs121908381(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

45331220

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs121908381
dbSNP (classic)	rs121908381
ClinGen	rs121908381
ebi	rs121908381
HLI	rs121908381
Exac	rs121908381
Gnomad	rs121908381
Varsome	rs121908381
LitVar	rs121908381
Map	rs121908381
PheGenI	rs121908381
Biobank	rs121908381
1000 genomes	rs121908381
hgdp	rs121908381
ensembl	rs121908381
geneview	rs121908381
scholar	rs121908381
google	rs121908381
pharmgkb	rs121908381
gwascentral	rs121908381
openSNP	rs121908381
23andMe	rs121908381
SNPshot	rs121908381
SNPdbe	rs121908381
MSV3d	rs121908381
GWAS Ctlg	rs121908381

Max Magnitude

3

OMIM	604933
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121908381(T;T)
Alt	rs121908381(T;T)
Reference	Rs121908381(G;G)
Significance	Pathogenic
Disease	MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MUTYH
CLNDBN	MYH-associated polyposis Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.45796892C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005618.6, RCV000222872.2, RCV000235388.2,