rs568149455

Orientation

plus

Stabilized

plus

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

Make rs568149455(A;A)

Make rs568149455(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

112838733

Gene

APC

is a	snp
is	mentioned by
dbSNP	rs568149455
dbSNP (classic)	rs568149455
ClinGen	rs568149455
ebi	rs568149455
HLI	rs568149455
Exac	rs568149455
Gnomad	rs568149455
Varsome	rs568149455
LitVar	rs568149455
Map	rs568149455
PheGenI	rs568149455
Biobank	rs568149455
1000 genomes	rs568149455
hgdp	rs568149455
ensembl	rs568149455
geneview	rs568149455
scholar	rs568149455
google	rs568149455
pharmgkb	rs568149455
gwascentral	rs568149455
openSNP	rs568149455
23andMe	rs568149455
SNPshot	rs568149455
SNPdbe	rs568149455
MSV3d	rs568149455
GWAS Ctlg	rs568149455

Max Magnitude

0

ClinVar
Risk	rs568149455(A;A) rs568149455(T;T)
Alt	rs568149455(A;A) rs568149455(T;T)
Reference	Rs568149455(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	APC
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.112174430G>T
CLNSRC
CLNACC	RCV000201963.1,