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rs786202276

From SNPedia

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Geno Mag Summary
(ACCA;ACCA) 0 common in clinvar
Make rs786202276(ACCA;TAC)
Make rs786202276(TAC;TAC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840418
GeneAPC
is asnp
is mentioned by
dbSNPrs786202276
ebirs786202276
HLIrs786202276
Exacrs786202276
Varsomers786202276
Maprs786202276
PheGenIrs786202276
hapmaprs786202276
1000 genomesrs786202276
hgdprs786202276
ensemblrs786202276
gopubmedrs786202276
geneviewrs786202276
scholarrs786202276
googlers786202276
pharmgkbrs786202276
gwascentralrs786202276
openSNPrs786202276
23andMers786202276
23andMe allrs786202276
SNP Nexus

SNPshotrs786202276
SNPdbers786202276
MSV3drs786202276
GWAS Ctlgrs786202276
Max Magnitude0
ClinVar
Risk rs786202276(TAC;TAC)
Alt rs786202276(TAC;TAC)
Reference rs786202276(ACCA;ACCA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112176115_112176118delACCAinsTAC
CLNSRC
CLNACC RCV000165005.1,