rs876660665

Orientation

plus

Stabilized

plus

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

Make rs876660665(A;T)

Make rs876660665(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

112841538

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs876660665
dbSNP (classic)	rs876660665
ClinGen	rs876660665
ebi	rs876660665
HLI	rs876660665
Exac	rs876660665
Gnomad	rs876660665
Varsome	rs876660665
LitVar	rs876660665
Map	rs876660665
PheGenI	rs876660665
Biobank	rs876660665
1000 genomes	rs876660665
hgdp	rs876660665
ensembl	rs876660665
geneview	rs876660665
scholar	rs876660665
google	rs876660665
pharmgkb	rs876660665
gwascentral	rs876660665
openSNP	rs876660665
23andMe	rs876660665
SNPshot	rs876660665
SNPdbe	rs876660665
MSV3d	rs876660665
GWAS Ctlg	rs876660665

Max Magnitude

0

ClinVar
Risk	rs876660665(T;T)
Alt	rs876660665(T;T)
Reference	Rs876660665(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112177235A>T
CLNSRC
CLNACC	RCV000217699.1,