rs863225362

Orientation

plus

Stabilized

plus

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

Make rs863225362(C;T)

Make rs863225362(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

112775693

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs863225362
dbSNP (classic)	rs863225362
ClinGen	rs863225362
ebi	rs863225362
HLI	rs863225362
Exac	rs863225362
Gnomad	rs863225362
Varsome	rs863225362
LitVar	rs863225362
Map	rs863225362
PheGenI	rs863225362
Biobank	rs863225362
1000 genomes	rs863225362
hgdp	rs863225362
ensembl	rs863225362
geneview	rs863225362
scholar	rs863225362
google	rs863225362
pharmgkb	rs863225362
gwascentral	rs863225362
openSNP	rs863225362
23andMe	rs863225362
SNPshot	rs863225362
SNPdbe	rs863225362
MSV3d	rs863225362
GWAS Ctlg	rs863225362

Max Magnitude

0

ClinVar
Risk	rs863225362(T;T)
Alt	rs863225362(T;T)
Reference	Rs863225362(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	APC
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.112111390C>T
CLNSRC
CLNACC	RCV000202083.1,