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rs730881247

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881247(C;G)
Make rs730881247(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839196
GeneAPC
is asnp
is mentioned by
dbSNPrs730881247
ebirs730881247
HLIrs730881247
Exacrs730881247
Varsomers730881247
Maprs730881247
PheGenIrs730881247
hapmaprs730881247
1000 genomesrs730881247
hgdprs730881247
ensemblrs730881247
gopubmedrs730881247
geneviewrs730881247
scholarrs730881247
googlers730881247
pharmgkbrs730881247
gwascentralrs730881247
openSNPrs730881247
23andMers730881247
23andMe allrs730881247
SNP Nexus

SNPshotrs730881247
SNPdbers730881247
MSV3drs730881247
GWAS Ctlgrs730881247
Max Magnitude0
ClinVar
Risk rs730881247(A,G;A,G)
Alt rs730881247(A,G;A,G)
Reference rs730881247(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174893C>A; NC_000005.9:g.112174893C>G
CLNSRC
CLNACC RCV000202226.1, RCV000159551.1,