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rs761458613

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761458613(G;T)
Make rs761458613(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112828973
GeneAPC
is asnp
is mentioned by
dbSNPrs761458613
ebirs761458613
HLIrs761458613
Exacrs761458613
Varsomers761458613
Maprs761458613
PheGenIrs761458613
hapmaprs761458613
1000 genomesrs761458613
hgdprs761458613
ensemblrs761458613
gopubmedrs761458613
geneviewrs761458613
scholarrs761458613
googlers761458613
pharmgkbrs761458613
gwascentralrs761458613
openSNPrs761458613
23andMers761458613
23andMe allrs761458613
SNP Nexus

SNPshotrs761458613
SNPdbers761458613
MSV3drs761458613
GWAS Ctlgrs761458613
Max Magnitude0
ClinVar
Risk rs761458613(A,T;A,T)
Alt rs761458613(A,T;A,T)
Reference rs761458613(G;G)
Significance Probable-Pathogenic
Disease Familial adenomatous polyposis 1 Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112164670G>A; NC_000005.9:g.112164670G>T
CLNSRC
CLNACC RCV000226069.1, RCV000217961.1,