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

rs876659452

From SNPedia

Orientationplus
Geno Mag Summary
(TTGTC;TTGTC) 0 common in clinvar
Make rs876659452(-;-)
Make rs876659452(-;TCTTG)
Make rs876659452(TCTTG;TCTTG)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112828883
GeneAPC
is asnp
is mentioned by
dbSNPrs876659452
ebirs876659452
HLIrs876659452
Exacrs876659452
Varsomers876659452
Maprs876659452
PheGenIrs876659452
hapmaprs876659452
1000 genomesrs876659452
hgdprs876659452
ensemblrs876659452
gopubmedrs876659452
geneviewrs876659452
scholarrs876659452
googlers876659452
pharmgkbrs876659452
gwascentralrs876659452
openSNPrs876659452
23andMers876659452
23andMe allrs876659452
SNP Nexus

SNPshotrs876659452
SNPdbers876659452
MSV3drs876659452
GWAS Ctlgrs876659452
Max Magnitude0
ClinVar
Risk rs876659452(;)
Alt rs876659452(;)
Reference rs876659452(TTGTC;TTGTC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112164580_112164584delTCTTG
CLNSRC
CLNACC RCV000217935.1,