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rs876658214

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658214(A;G)
Make rs876658214(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112837551
GeneAPC
is asnp
is mentioned by
dbSNPrs876658214
ebirs876658214
HLIrs876658214
Exacrs876658214
Varsomers876658214
Maprs876658214
PheGenIrs876658214
hapmaprs876658214
1000 genomesrs876658214
hgdprs876658214
ensemblrs876658214
gopubmedrs876658214
geneviewrs876658214
scholarrs876658214
googlers876658214
pharmgkbrs876658214
gwascentralrs876658214
openSNPrs876658214
23andMers876658214
23andMe allrs876658214
SNP Nexus

SNPshotrs876658214
SNPdbers876658214
MSV3drs876658214
GWAS Ctlgrs876658214
Max Magnitude0
ClinVar
Risk rs876658214(G;G)
Alt rs876658214(G;G)
Reference rs876658214(A;A)
Significance Probable-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.112173248A>G
CLNSRC
CLNACC RCV000220818.1,