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rs758987855

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs758987855(G;T)
Make rs758987855(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112840581
GeneAPC
is asnp
is mentioned by
dbSNPrs758987855
ebirs758987855
HLIrs758987855
Exacrs758987855
Varsomers758987855
Maprs758987855
PheGenIrs758987855
hapmaprs758987855
1000 genomesrs758987855
hgdprs758987855
ensemblrs758987855
gopubmedrs758987855
geneviewrs758987855
scholarrs758987855
googlers758987855
pharmgkbrs758987855
gwascentralrs758987855
openSNPrs758987855
23andMers758987855
23andMe allrs758987855
SNP Nexus

SNPshotrs758987855
SNPdbers758987855
MSV3drs758987855
GWAS Ctlgrs758987855
Max Magnitude0
ClinVar
Risk rs758987855(A,T;A,T)
Alt rs758987855(A,T;A,T)
Reference rs758987855(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112176278G>A; NC_000005.9:g.112176278G>T
CLNSRC
CLNACC RCV000195952.1, RCV000227078.1,