rs876658868

Orientation

plus

Stabilized

plus

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

Make rs876658868(C;T)

Make rs876658868(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

112827116

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs876658868
dbSNP (classic)	rs876658868
ClinGen	rs876658868
ebi	rs876658868
HLI	rs876658868
Exac	rs876658868
Gnomad	rs876658868
Varsome	rs876658868
LitVar	rs876658868
Map	rs876658868
PheGenI	rs876658868
Biobank	rs876658868
1000 genomes	rs876658868
hgdp	rs876658868
ensembl	rs876658868
geneview	rs876658868
scholar	rs876658868
google	rs876658868
pharmgkb	rs876658868
gwascentral	rs876658868
openSNP	rs876658868
23andMe	rs876658868
SNPshot	rs876658868
SNPdbe	rs876658868
MSV3d	rs876658868
GWAS Ctlg	rs876658868

Max Magnitude

0

ClinVar
Risk	rs876658868(T;T)
Alt	rs876658868(T;T)
Reference	Rs876658868(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112162813C>T
CLNSRC
CLNACC	RCV000219498.2,