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

rs876660130

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660130(C;T)
Make rs876660130(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112837593
GeneAPC
is asnp
is mentioned by
dbSNPrs876660130
ebirs876660130
HLIrs876660130
Exacrs876660130
Varsomers876660130
Maprs876660130
PheGenIrs876660130
hapmaprs876660130
1000 genomesrs876660130
hgdprs876660130
ensemblrs876660130
gopubmedrs876660130
geneviewrs876660130
scholarrs876660130
googlers876660130
pharmgkbrs876660130
gwascentralrs876660130
openSNPrs876660130
23andMers876660130
23andMe allrs876660130
SNP Nexus

SNPshotrs876660130
SNPdbers876660130
MSV3drs876660130
GWAS Ctlgrs876660130
Max Magnitude0
ClinVar
Risk rs876660130(T;T)
Alt rs876660130(T;T)
Reference rs876660130(C;C)
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.112173290C>T
CLNSRC
CLNACC RCV000213199.1,