rs876659676

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs876659676(A;G)

Make rs876659676(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

45332252

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs876659676
dbSNP (classic)	rs876659676
ClinGen	rs876659676
ebi	rs876659676
HLI	rs876659676
Exac	rs876659676
Gnomad	rs876659676
Varsome	rs876659676
LitVar	rs876659676
Map	rs876659676
PheGenI	rs876659676
Biobank	rs876659676
1000 genomes	rs876659676
hgdp	rs876659676
ensembl	rs876659676
geneview	rs876659676
scholar	rs876659676
google	rs876659676
pharmgkb	rs876659676
gwascentral	rs876659676
openSNP	rs876659676
23andMe	rs876659676
SNPshot	rs876659676
SNPdbe	rs876659676
MSV3d	rs876659676
GWAS Ctlg	rs876659676

Max Magnitude

0

ClinVar
Risk	rs876659676(G;G)
Alt	rs876659676(G;G)
Reference	Rs876659676(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.45797924T>C
CLNSRC
CLNACC	RCV000216419.1, RCV000479475.1,