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rs786201118

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs786201118(-;-)
Make rs786201118(-;AT)
Make rs786201118(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840263
GeneAPC
is asnp
is mentioned by
dbSNPrs786201118
ebirs786201118
HLIrs786201118
Exacrs786201118
Varsomers786201118
Maprs786201118
PheGenIrs786201118
hapmaprs786201118
1000 genomesrs786201118
hgdprs786201118
ensemblrs786201118
gopubmedrs786201118
geneviewrs786201118
scholarrs786201118
googlers786201118
pharmgkbrs786201118
gwascentralrs786201118
openSNPrs786201118
23andMers786201118
23andMe allrs786201118
SNP Nexus

SNPshotrs786201118
SNPdbers786201118
MSV3drs786201118
GWAS Ctlgrs786201118
Max Magnitude0
ClinVar
Risk rs786201118(;)
Alt rs786201118(;)
Reference rs786201118(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.112175960_112175961delAT
CLNSRC
CLNACC RCV000162703.1,