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rs876660174

From SNPedia

Orientationplus
Geno Mag Summary
(GTTT;GTTT) 0 common in clinvar
Make rs876660174(-;-)
Make rs876660174(-;GTTT)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112841653
GeneAPC
is asnp
is mentioned by
dbSNPrs876660174
ebirs876660174
HLIrs876660174
Exacrs876660174
Varsomers876660174
Maprs876660174
PheGenIrs876660174
hapmaprs876660174
1000 genomesrs876660174
hgdprs876660174
ensemblrs876660174
gopubmedrs876660174
geneviewrs876660174
scholarrs876660174
googlers876660174
pharmgkbrs876660174
gwascentralrs876660174
openSNPrs876660174
23andMers876660174
23andMe allrs876660174
SNP Nexus

SNPshotrs876660174
SNPdbers876660174
MSV3drs876660174
GWAS Ctlgrs876660174
Max Magnitude0
ClinVar
Risk rs876660174(;)
Alt rs876660174(;)
Reference rs876660174(GTTT;GTTT)
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.112177350_112177353delGTTT
CLNSRC
CLNACC RCV000216176.1,