rs587779780

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6.5	Familial Adenomatous Polyposis

Make rs587779780(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

112819245

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs587779780
dbSNP (classic)	rs587779780
ClinGen	rs587779780
ebi	rs587779780
HLI	rs587779780
Exac	rs587779780
Gnomad	rs587779780
Varsome	rs587779780
LitVar	rs587779780
Map	rs587779780
PheGenI	rs587779780
Biobank	rs587779780
1000 genomes	rs587779780
hgdp	rs587779780
ensembl	rs587779780
geneview	rs587779780
scholar	rs587779780
google	rs587779780
pharmgkb	rs587779780
gwascentral	rs587779780
openSNP	rs587779780
23andMe	rs587779780
SNPshot	rs587779780
SNPdbe	rs587779780
MSV3d	rs587779780
GWAS Ctlg	rs587779780

Max Magnitude

6.5

ClinVar
Risk	rs587779780(T;T)
Alt	rs587779780(T;T)
Reference	Rs587779780(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Reversed	0
HGVS	NC_000005.9:g.112154942C>T
CLNSRC
CLNACC	RCV000115066.7, RCV000202096.2, RCV000234357.2,