rs869312771

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CAGGGAGGAGAGCTCTGCC;CAGGGAGGAGAGCTCTGCC)	0	common in clinvar
(CAGGGAGGAGAGCTCTGCCA;CAGGGAGGAGAGCTCTGCCA)	0	common in clinvar

Make rs869312771(-;-)

Make rs869312771(-;CAGGGAGGAGAGCTCTGCC)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

45331728

Gene

MUTYH

is a	snp
is	mentioned by
dbSNP	rs869312771
dbSNP (classic)	rs869312771
ClinGen	rs869312771
ebi	rs869312771
HLI	rs869312771
Exac	rs869312771
Gnomad	rs869312771
Varsome	rs869312771
LitVar	rs869312771
Map	rs869312771
PheGenI	rs869312771
Biobank	rs869312771
1000 genomes	rs869312771
hgdp	rs869312771
ensembl	rs869312771
geneview	rs869312771
scholar	rs869312771
google	rs869312771
pharmgkb	rs869312771
gwascentral	rs869312771
openSNP	rs869312771
23andMe	rs869312771
SNPshot	rs869312771
SNPdbe	rs869312771
MSV3d	rs869312771
GWAS Ctlg	rs869312771

Max Magnitude

0

ClinVar
Risk	rs869312771(-;-)
Alt	rs869312771(-;-)
Reference	Rs869312771(CAGGGAGGAGAGCTCTGCC;CAGGGAGGAGAGCTCTGCC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MUTYH
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000001.10:g.45797400_45797418del19
CLNSRC
CLNACC	RCV000210110.1,