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rs876660496

From SNPedia

Orientationplus
Geno Mag Summary
(TCAAA;TCAAA) 0 common in clinvar
Make rs876660496(-;-)
Make rs876660496(-;CAAAT)
Make rs876660496(CAAAT;CAAAT)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838473
GeneAPC
is asnp
is mentioned by
dbSNPrs876660496
ebirs876660496
HLIrs876660496
Exacrs876660496
Varsomers876660496
Maprs876660496
PheGenIrs876660496
hapmaprs876660496
1000 genomesrs876660496
hgdprs876660496
ensemblrs876660496
gopubmedrs876660496
geneviewrs876660496
scholarrs876660496
googlers876660496
pharmgkbrs876660496
gwascentralrs876660496
openSNPrs876660496
23andMers876660496
23andMe allrs876660496
SNP Nexus

SNPshotrs876660496
SNPdbers876660496
MSV3drs876660496
GWAS Ctlgrs876660496
Max Magnitude0
ClinVar
Risk rs876660496(;)
Alt rs876660496(;)
Reference rs876660496(TCAAA;TCAAA)
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.112174170_112174174delCAAAT
CLNSRC
CLNACC RCV000221207.1,