rs137854575

Orientation

plus

Stabilized

plus

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

Make rs137854575(C;T)

Make rs137854575(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

112838399

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs137854575
dbSNP (classic)	rs137854575
ClinGen	rs137854575
ebi	rs137854575
HLI	rs137854575
Exac	rs137854575
Gnomad	rs137854575
Varsome	rs137854575
LitVar	rs137854575
Map	rs137854575
PheGenI	rs137854575
Biobank	rs137854575
1000 genomes	rs137854575
hgdp	rs137854575
ensembl	rs137854575
geneview	rs137854575
scholar	rs137854575
google	rs137854575
pharmgkb	rs137854575
gwascentral	rs137854575
openSNP	rs137854575
23andMe	rs137854575
23andMe all	rs137854575
SNPshot	rs137854575
SNPdbe	rs137854575
MSV3d	rs137854575
GWAS Ctlg	rs137854575

GMAF

0.0004591

Max Magnitude

0

OMIM	611731
Desc
Variant	0018
Related	also

ClinVar
Risk	rs137854575(A;A) rs137854575(G;G) rs137854575(T;T)
Alt	rs137854575(A;A) rs137854575(G;G) rs137854575(T;T)
Reference	Rs137854575(C;C)
Significance	Other
Disease	Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome not provided Colorectal cancer Familial multiple polyposis syndrome not specified
Variation	info
Gene	APC
CLNDBN	Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome not provided Colorectal cancer, susceptibility to Familial multiple polyposis syndrome not specified
Reversed	0
HGVS	NC_000005.9:g.112174096C>A; NC_000005.9:g.112174096C>G; NC_000005.9:g.112174096C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000848.3, RCV000129305.6, RCV000202012.2, RCV000210151.1, RCV000165582.2, RCV000202153.1, RCV000123663.5, RCV000199328.4, RCV000202773.1, RCV000211904.1,