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rs786202348

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs786202348(-;-)
Make rs786202348(-;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839080
GeneAPC
is asnp
is mentioned by
dbSNPrs786202348
ebirs786202348
HLIrs786202348
Exacrs786202348
Varsomers786202348
Maprs786202348
PheGenIrs786202348
hapmaprs786202348
1000 genomesrs786202348
hgdprs786202348
ensemblrs786202348
gopubmedrs786202348
geneviewrs786202348
scholarrs786202348
googlers786202348
pharmgkbrs786202348
gwascentralrs786202348
openSNPrs786202348
23andMers786202348
23andMe allrs786202348
SNP Nexus

SNPshotrs786202348
SNPdbers786202348
MSV3drs786202348
GWAS Ctlgrs786202348
Max Magnitude0
ClinVar
Risk rs786202348(;)
Alt rs786202348(;)
Reference rs786202348(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174777_112174778delTA
CLNSRC
CLNACC RCV000165111.1,