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rs730881227

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881227(A;A)
Make rs730881227(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112779849
GeneAPC
is asnp
is mentioned by
dbSNPrs730881227
ebirs730881227
HLIrs730881227
Exacrs730881227
Varsomers730881227
Maprs730881227
PheGenIrs730881227
hapmaprs730881227
1000 genomesrs730881227
hgdprs730881227
ensemblrs730881227
gopubmedrs730881227
geneviewrs730881227
scholarrs730881227
googlers730881227
pharmgkbrs730881227
gwascentralrs730881227
openSNPrs730881227
23andMers730881227
23andMe allrs730881227
SNP Nexus

SNPshotrs730881227
SNPdbers730881227
MSV3drs730881227
GWAS Ctlgrs730881227
Max Magnitude0
ClinVar
Risk rs730881227(A;A)
Alt rs730881227(A;A)
Reference rs730881227(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.112115546G>A
CLNSRC
CLNACC RCV000159516.1,