Have questions? Visit https://www.reddit.com/r/SNPedia

rs568149455

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs568149455(A;A)
Make rs568149455(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838733
GeneAPC
is asnp
is mentioned by
dbSNPrs568149455
ebirs568149455
HLIrs568149455
Exacrs568149455
Varsomers568149455
Maprs568149455
PheGenIrs568149455
hapmaprs568149455
1000 genomesrs568149455
hgdprs568149455
ensemblrs568149455
gopubmedrs568149455
geneviewrs568149455
scholarrs568149455
googlers568149455
pharmgkbrs568149455
gwascentralrs568149455
openSNPrs568149455
23andMers568149455
23andMe allrs568149455
SNP Nexus

SNPshotrs568149455
SNPdbers568149455
MSV3drs568149455
GWAS Ctlgrs568149455
Max Magnitude0
ClinVar
Risk rs568149455(A,T;A,T)
Alt rs568149455(A,T;A,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,