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rs76601225

From SNPedia

Orientationplus
Make rs76601225(A;A)
Make rs76601225(A;C)
Make rs76601225(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112811070
GeneAPC
is asnp
is mentioned by
dbSNPrs76601225
ebirs76601225
HLIrs76601225
Exacrs76601225
Varsomers76601225
Maprs76601225
PheGenIrs76601225
hapmaprs76601225
1000 genomesrs76601225
hgdprs76601225
ensemblrs76601225
gopubmedrs76601225
geneviewrs76601225
scholarrs76601225
googlers76601225
pharmgkbrs76601225
gwascentralrs76601225
openSNPrs76601225
23andMers76601225
23andMe allrs76601225
SNP Nexus

SNPshotrs76601225
SNPdbers76601225
MSV3drs76601225
GWAS Ctlgrs76601225
Max Magnitude
ClinVar
Risk rs76601225(C;C)
Alt rs76601225(C;C)
Reference rs76601225(A;A)
Significance Other
Disease Familial colorectal cancer
Variation info
Gene APC
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_000005.9:g.112146767A>C
CLNSRC
CLNACC RCV000073532.1,