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rs863225338

From SNPedia

Orientationplus
Make rs863225338(-;-)
Make rs863225338(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838719
GeneAPC
is asnp
is mentioned by
dbSNPrs863225338
ebirs863225338
HLIrs863225338
Exacrs863225338
Varsomers863225338
Maprs863225338
PheGenIrs863225338
hapmaprs863225338
1000 genomesrs863225338
hgdprs863225338
ensemblrs863225338
gopubmedrs863225338
geneviewrs863225338
scholarrs863225338
googlers863225338
pharmgkbrs863225338
gwascentralrs863225338
openSNPrs863225338
23andMers863225338
23andMe allrs863225338
SNP Nexus

SNPshotrs863225338
SNPdbers863225338
MSV3drs863225338
GWAS Ctlgrs863225338
Max Magnitude
ClinVar
Risk rs863225338(;)
Alt rs863225338(;)
Reference rs863225338(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174416delG
CLNSRC
CLNACC RCV000202061.1,