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rs863225341

From SNPedia

Orientationplus
Make rs863225341(-;-)
Make rs863225341(-;TCTC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838892
GeneAPC
is asnp
is mentioned by
dbSNPrs863225341
ebirs863225341
HLIrs863225341
Exacrs863225341
Varsomers863225341
Maprs863225341
PheGenIrs863225341
hapmaprs863225341
1000 genomesrs863225341
hgdprs863225341
ensemblrs863225341
gopubmedrs863225341
geneviewrs863225341
scholarrs863225341
googlers863225341
pharmgkbrs863225341
gwascentralrs863225341
openSNPrs863225341
23andMers863225341
23andMe allrs863225341
SNP Nexus

SNPshotrs863225341
SNPdbers863225341
MSV3drs863225341
GWAS Ctlgrs863225341
Max Magnitude
ClinVar
Risk rs863225341(;)
Alt rs863225341(;)
Reference rs863225341(TCTC;TCTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174589_112174592delTCTC
CLNSRC
CLNACC RCV000202195.1,