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rs79619757

From SNPedia

Orientationplus
Make rs79619757(G;G)
Make rs79619757(G;T)
Make rs79619757(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112843567
GeneAPC
is asnp
is mentioned by
dbSNPrs79619757
ebirs79619757
HLIrs79619757
Exacrs79619757
Varsomers79619757
Maprs79619757
PheGenIrs79619757
hapmaprs79619757
1000 genomesrs79619757
hgdprs79619757
ensemblrs79619757
gopubmedrs79619757
geneviewrs79619757
scholarrs79619757
googlers79619757
pharmgkbrs79619757
gwascentralrs79619757
openSNPrs79619757
23andMers79619757
23andMe allrs79619757
SNP Nexus

SNPshotrs79619757
SNPdbers79619757
MSV3drs79619757
GWAS Ctlgrs79619757
Max Magnitude
ClinVar
Risk rs79619757(T;T)
Alt rs79619757(T;T)
Reference rs79619757(G;G)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112179264G>T
CLNSRC
CLNACC RCV000074245.1,