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rs79630786

From SNPedia

Orientationplus
Make rs79630786(C;C)
Make rs79630786(C;G)
Make rs79630786(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112843107
GeneAPC
is asnp
is mentioned by
dbSNPrs79630786
ebirs79630786
HLIrs79630786
Exacrs79630786
Varsomers79630786
Maprs79630786
PheGenIrs79630786
hapmaprs79630786
1000 genomesrs79630786
hgdprs79630786
ensemblrs79630786
gopubmedrs79630786
geneviewrs79630786
scholarrs79630786
googlers79630786
pharmgkbrs79630786
gwascentralrs79630786
openSNPrs79630786
23andMers79630786
23andMe allrs79630786
SNP Nexus

SNPshotrs79630786
SNPdbers79630786
MSV3drs79630786
GWAS Ctlgrs79630786
Max Magnitude
ClinVar
Risk rs79630786(G;G)
Alt rs79630786(G;G)
Reference rs79630786(C;C)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112178804C>G
CLNSRC
CLNACC RCV000073624.1,