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rs786202995

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202995(G;T)
Make rs786202995(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838565
GeneAPC
is asnp
is mentioned by
dbSNPrs786202995
ebirs786202995
HLIrs786202995
Exacrs786202995
Varsomers786202995
Maprs786202995
PheGenIrs786202995
hapmaprs786202995
1000 genomesrs786202995
hgdprs786202995
ensemblrs786202995
gopubmedrs786202995
geneviewrs786202995
scholarrs786202995
googlers786202995
pharmgkbrs786202995
gwascentralrs786202995
openSNPrs786202995
23andMers786202995
23andMe allrs786202995
SNP Nexus

SNPshotrs786202995
SNPdbers786202995
MSV3drs786202995
GWAS Ctlgrs786202995
Max Magnitude0
ClinVar
Risk rs786202995(T;T)
Alt rs786202995(T;T)
Reference rs786202995(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174262G>T
CLNSRC
CLNACC RCV000166096.1,