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rs414098

From SNPedia

Orientationplus
Make rs414098(A;A)
Make rs414098(A;G)
Make rs414098(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112778075
GeneAPC
is asnp
is mentioned by
dbSNPrs414098
ebirs414098
HLIrs414098
Exacrs414098
Varsomers414098
Maprs414098
PheGenIrs414098
hapmaprs414098
1000 genomesrs414098
hgdprs414098
ensemblrs414098
gopubmedrs414098
geneviewrs414098
scholarrs414098
googlers414098
pharmgkbrs414098
gwascentralrs414098
openSNPrs414098
23andMers414098
23andMe allrs414098
SNP Nexus

SNPshotrs414098
SNPdbers414098
MSV3drs414098
GWAS Ctlgrs414098
Max Magnitude
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs414098(A;A)
Alt rs414098(A;A)
Reference rs414098(G;G)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112113772G>A
CLNSRC
CLNACC RCV000073916.1,