rs137854569

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	6.5	Familial Adenomatous Polyposis

Make rs137854569(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

112815499

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs137854569
dbSNP (classic)	rs137854569
ClinGen	rs137854569
ebi	rs137854569
HLI	rs137854569
Exac	rs137854569
Gnomad	rs137854569
Varsome	rs137854569
LitVar	rs137854569
Map	rs137854569
PheGenI	rs137854569
Biobank	rs137854569
1000 genomes	rs137854569
hgdp	rs137854569
ensembl	rs137854569
geneview	rs137854569
scholar	rs137854569
google	rs137854569
pharmgkb	rs137854569
gwascentral	rs137854569
openSNP	rs137854569
23andMe	rs137854569
SNPshot	rs137854569
SNPdbe	rs137854569
MSV3d	rs137854569
GWAS Ctlg	rs137854569

Max Magnitude

6.5

OMIM	611731
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137854569(G;G) rs137854569(T;T)
Alt	rs137854569(G;G) rs137854569(T;T)
Reference	Rs137854569(C;C)
Significance	Pathogenic
Disease	Gardner syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	APC
CLNDBN	Gardner syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.112151196C>G; NC_000005.9:g.112151196C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000836.5, RCV000218327.1,