rs185154886

Orientation

plus

Stabilized

plus

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

Make rs185154886(C;C)

Make rs185154886(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

112780831

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs185154886
dbSNP (classic)	rs185154886
ClinGen	rs185154886
ebi	rs185154886
HLI	rs185154886
Exac	rs185154886
Gnomad	rs185154886
Varsome	rs185154886
LitVar	rs185154886
Map	rs185154886
PheGenI	rs185154886
Biobank	rs185154886
1000 genomes	rs185154886
hgdp	rs185154886
ensembl	rs185154886
geneview	rs185154886
scholar	rs185154886
google	rs185154886
pharmgkb	rs185154886
gwascentral	rs185154886
openSNP	rs185154886
23andMe	rs185154886
SNPshot	rs185154886
SNPdbe	rs185154886
MSV3d	rs185154886
GWAS Ctlg	rs185154886

Max Magnitude

0

ClinVar
Risk	rs185154886(A;A) rs185154886(C;C)
Alt	rs185154886(A;A) rs185154886(C;C)
Reference	Rs185154886(T;T)
Significance	Probable-Pathogenic
Disease	not provided Familial adenomatous polyposis 1 APC-Associated Polyposis Disorders not specified
Variation	info
Gene	APC
CLNDBN	not provided Familial adenomatous polyposis 1 APC-Associated Polyposis Disorders not specified
Reversed	0
HGVS	NC_000005.9:g.112116528T>A; NC_000005.9:g.112116528T>C
CLNSRC	Illumina
CLNACC	RCV000255000.1, RCV000197836.3, RCV000309947.1, RCV000426052.1,