rs768922431

Orientation

plus

Stabilized

plus

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

Make rs768922431(C;T)

Make rs768922431(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

112842303

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs768922431
dbSNP (classic)	rs768922431
ClinGen	rs768922431
ebi	rs768922431
HLI	rs768922431
Exac	rs768922431
Gnomad	rs768922431
Varsome	rs768922431
LitVar	rs768922431
Map	rs768922431
PheGenI	rs768922431
Biobank	rs768922431
1000 genomes	rs768922431
hgdp	rs768922431
ensembl	rs768922431
geneview	rs768922431
scholar	rs768922431
google	rs768922431
pharmgkb	rs768922431
gwascentral	rs768922431
openSNP	rs768922431
23andMe	rs768922431
SNPshot	rs768922431
SNPdbe	rs768922431
MSV3d	rs768922431
GWAS Ctlg	rs768922431

Max Magnitude

0

ClinVar
Risk	rs768922431(A;A) rs768922431(T;T)
Alt	rs768922431(A;A) rs768922431(T;T)
Reference	Rs768922431(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	APC
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000005.9:g.112178000C>A; NC_000005.9:g.112178000C>T
CLNSRC
CLNACC	RCV000219807.1, RCV000167356.1, RCV000237046.1,