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rs387906236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs387906236(-;-)
Make rs387906236(-;AG)
ReferenceGRCh38 38.1/141
Chromosome5
Position112840205
GeneAPC
is asnp
is mentioned by
dbSNPrs387906236
ebirs387906236
HLIrs387906236
Exacrs387906236
Varsomers387906236
Maprs387906236
PheGenIrs387906236
hapmaprs387906236
1000 genomesrs387906236
hgdprs387906236
ensemblrs387906236
gopubmedrs387906236
geneviewrs387906236
scholarrs387906236
googlers387906236
pharmgkbrs387906236
gwascentralrs387906236
openSNPrs387906236
23andMers387906236
23andMe allrs387906236
SNP Nexus

SNPshotrs387906236
SNPdbers387906236
MSV3drs387906236
GWAS Ctlgrs387906236
Max Magnitude0
ClinVar
Risk rs387906236(;)
Alt rs387906236(;)
Reference rs387906236(AG;AG)
Significance Pathogenic
Disease Gardner syndrome
Variation info
Gene APC
CLNDBN Gardner syndrome
Reversed 0
HGVS NC_000005.9:g.112175902_112175903delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000866.3,