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rs876659647

From SNPedia

Orientationplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs876659647(-;-)
Make rs876659647(-;GAAA)
Make rs876659647(GAAA;GAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112839519
GeneAPC
is asnp
is mentioned by
dbSNPrs876659647
ebirs876659647
HLIrs876659647
Exacrs876659647
Varsomers876659647
Maprs876659647
PheGenIrs876659647
hapmaprs876659647
1000 genomesrs876659647
hgdprs876659647
ensemblrs876659647
gopubmedrs876659647
geneviewrs876659647
scholarrs876659647
googlers876659647
pharmgkbrs876659647
gwascentralrs876659647
openSNPrs876659647
23andMers876659647
23andMe allrs876659647
SNP Nexus

SNPshotrs876659647
SNPdbers876659647
MSV3drs876659647
GWAS Ctlgrs876659647
Max Magnitude0
ClinVar
Risk rs876659647(;)
Alt rs876659647(;)
Reference rs876659647(AAAG;AAAG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175216_112175219delGAAA
CLNSRC
CLNACC RCV000221539.1, RCV000232837.1,