rs145945630

Orientation

plus

Stabilized

plus

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

Make rs145945630(C;T)

Make rs145945630(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

112754960

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs145945630
dbSNP (classic)	rs145945630
ClinGen	rs145945630
ebi	rs145945630
HLI	rs145945630
Exac	rs145945630
Gnomad	rs145945630
Varsome	rs145945630
LitVar	rs145945630
Map	rs145945630
PheGenI	rs145945630
Biobank	rs145945630
1000 genomes	rs145945630
hgdp	rs145945630
ensembl	rs145945630
geneview	rs145945630
scholar	rs145945630
google	rs145945630
pharmgkb	rs145945630
gwascentral	rs145945630
openSNP	rs145945630
23andMe	rs145945630
SNPshot	rs145945630
SNPdbe	rs145945630
MSV3d	rs145945630
GWAS Ctlg	rs145945630

Max Magnitude

0

ClinVar
Risk	rs145945630(T;T)
Alt	rs145945630(T;T)
Reference	Rs145945630(C;C)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 not provided
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 not provided
Reversed	0
HGVS	NC_000005.9:g.112090657C>T
CLNSRC
CLNACC	RCV000164002.3, RCV000227124.2, RCV000482864.1,