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rs78897872

From SNPedia

Orientationplus
Make rs78897872(A;A)
Make rs78897872(A;C)
Make rs78897872(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112834387
GeneAPC
is asnp
is mentioned by
dbSNPrs78897872
ebirs78897872
HLIrs78897872
Exacrs78897872
Varsomers78897872
Maprs78897872
PheGenIrs78897872
hapmaprs78897872
1000 genomesrs78897872
hgdprs78897872
ensemblrs78897872
gopubmedrs78897872
geneviewrs78897872
scholarrs78897872
googlers78897872
pharmgkbrs78897872
gwascentralrs78897872
openSNPrs78897872
23andMers78897872
23andMe allrs78897872
SNP Nexus

SNPshotrs78897872
SNPdbers78897872
MSV3drs78897872
GWAS Ctlgrs78897872
Max Magnitude
ClinVar
Risk rs78897872(C;C)
Alt rs78897872(C;C)
Reference rs78897872(A;A)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112170084A>C
CLNSRC
CLNACC RCV000074195.1,