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rs75612255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs75612255(C;C)
Make rs75612255(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112737543
GeneAPC
is asnp
is mentioned by
dbSNPrs75612255
ebirs75612255
HLIrs75612255
Exacrs75612255
Varsomers75612255
Maprs75612255
PheGenIrs75612255
hapmaprs75612255
1000 genomesrs75612255
hgdprs75612255
ensemblrs75612255
gopubmedrs75612255
geneviewrs75612255
scholarrs75612255
googlers75612255
pharmgkbrs75612255
gwascentralrs75612255
openSNPrs75612255
23andMers75612255
23andMe allrs75612255
SNP Nexus

SNPshotrs75612255
SNPdbers75612255
MSV3drs75612255
GWAS Ctlgrs75612255
Max Magnitude0
ClinVar
Risk rs75612255(C;C)
Alt rs75612255(C;C)
Reference rs75612255(T;T)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112073240T>C
CLNSRC ClinVar
CLNACC RCV000073721.1,