rs876658724

Orientation

plus

Stabilized

plus

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

Make rs876658724(-;A)

Make rs876658724(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

112838661

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs876658724
dbSNP (classic)	rs876658724
ClinGen	rs876658724
ebi	rs876658724
HLI	rs876658724
Exac	rs876658724
Gnomad	rs876658724
Varsome	rs876658724
LitVar	rs876658724
Map	rs876658724
PheGenI	rs876658724
Biobank	rs876658724
1000 genomes	rs876658724
hgdp	rs876658724
ensembl	rs876658724
geneview	rs876658724
scholar	rs876658724
google	rs876658724
pharmgkb	rs876658724
gwascentral	rs876658724
openSNP	rs876658724
23andMe	rs876658724
SNPshot	rs876658724
SNPdbe	rs876658724
MSV3d	rs876658724
GWAS Ctlg	rs876658724

Max Magnitude

0

ClinVar
Risk	rs876658724(A;A)
Alt	rs876658724(A;A)
Reference	Rs876658724(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112174358dupA
CLNSRC
CLNACC	RCV000214795.1,