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rs786203760

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs786203760(-;-)
Make rs786203760(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839401
GeneAPC
is asnp
is mentioned by
dbSNPrs786203760
ebirs786203760
HLIrs786203760
Exacrs786203760
Varsomers786203760
Maprs786203760
PheGenIrs786203760
hapmaprs786203760
1000 genomesrs786203760
hgdprs786203760
ensemblrs786203760
gopubmedrs786203760
geneviewrs786203760
scholarrs786203760
googlers786203760
pharmgkbrs786203760
gwascentralrs786203760
openSNPrs786203760
23andMers786203760
23andMe allrs786203760
SNP Nexus

SNPshotrs786203760
SNPdbers786203760
MSV3drs786203760
GWAS Ctlgrs786203760
Max Magnitude0
ClinVar
Risk rs786203760(;)
Alt rs786203760(;)
Reference rs786203760(AT;AT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000005.9:g.112175098_112175099delAT
CLNSRC
CLNACC RCV000167206.1, RCV000202002.1,