rs587779798

Orientation

plus

Stabilized

plus

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

Make rs587779798(A;A)

Make rs587779798(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

112775742

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs587779798
dbSNP (classic)	rs587779798
ClinGen	rs587779798
ebi	rs587779798
HLI	rs587779798
Exac	rs587779798
Gnomad	rs587779798
Varsome	rs587779798
LitVar	rs587779798
Map	rs587779798
PheGenI	rs587779798
Biobank	rs587779798
1000 genomes	rs587779798
hgdp	rs587779798
ensembl	rs587779798
geneview	rs587779798
scholar	rs587779798
google	rs587779798
pharmgkb	rs587779798
gwascentral	rs587779798
openSNP	rs587779798
23andMe	rs587779798
SNPshot	rs587779798
SNPdbe	rs587779798
MSV3d	rs587779798
GWAS Ctlg	rs587779798

Max Magnitude

0

ClinVar
Risk	rs587779798(A;A) rs587779798(C;C)
Alt	rs587779798(A;A) rs587779798(C;C)
Reference	Rs587779798(G;G)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112111439G>A; NC_000005.9:g.112111439G>C
CLNSRC
CLNACC	RCV000115103.5, RCV000322468.1, RCV000491896.1,