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rs79707630

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs79707630(A;A)
Make rs79707630(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position112727897
GeneAPC
is asnp
is mentioned by
dbSNPrs79707630
ebirs79707630
HLIrs79707630
Exacrs79707630
Varsomers79707630
Maprs79707630
PheGenIrs79707630
hapmaprs79707630
1000 genomesrs79707630
hgdprs79707630
ensemblrs79707630
gopubmedrs79707630
geneviewrs79707630
scholarrs79707630
googlers79707630
pharmgkbrs79707630
gwascentralrs79707630
openSNPrs79707630
23andMers79707630
23andMe allrs79707630
SNP Nexus

SNPshotrs79707630
SNPdbers79707630
MSV3drs79707630
GWAS Ctlgrs79707630
Max Magnitude0
ClinVar
Risk rs79707630(A,T;A,T)
Alt rs79707630(A,T;A,T)
Reference rs79707630(G;G)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112063594G>A; NC_000005.9:g.112063594G>T
CLNSRC ClinVar
CLNACC RCV000073685.1, RCV000073277.1,