rs376213437

Orientation

plus

Stabilized

plus

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

Make rs376213437(C;C)

Make rs376213437(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

112767256

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs376213437
dbSNP (classic)	rs376213437
ClinGen	rs376213437
ebi	rs376213437
HLI	rs376213437
Exac	rs376213437
Gnomad	rs376213437
Varsome	rs376213437
LitVar	rs376213437
Map	rs376213437
PheGenI	rs376213437
Biobank	rs376213437
1000 genomes	rs376213437
hgdp	rs376213437
ensembl	rs376213437
geneview	rs376213437
scholar	rs376213437
google	rs376213437
pharmgkb	rs376213437
gwascentral	rs376213437
openSNP	rs376213437
23andMe	rs376213437
SNPshot	rs376213437
SNPdbe	rs376213437
MSV3d	rs376213437
GWAS Ctlg	rs376213437

Max Magnitude

0

ClinVar
Risk	rs376213437(A;A) rs376213437(C;C) rs376213437(G;G)
Alt	rs376213437(A;A) rs376213437(C;C) rs376213437(G;G)
Reference	Rs376213437(T;T)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 not specified
Variation	info
Gene	APC
CLNDBN	not provided Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 not specified
Reversed	0
HGVS	NC_000005.9:g.112102953T>A; NC_000005.9:g.112102953T>C; NC_000005.9:g.112102953T>G
CLNSRC
CLNACC	RCV000159585.2, RCV000165334.1, RCV000205434.2, RCV000427257.1, RCV000202141.1, RCV000491545.1,