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rs756912930

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756912930(G;T)
Make rs756912930(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840089
GeneAPC
is asnp
is mentioned by
dbSNPrs756912930
ebirs756912930
HLIrs756912930
Exacrs756912930
Varsomers756912930
Maprs756912930
PheGenIrs756912930
hapmaprs756912930
1000 genomesrs756912930
hgdprs756912930
ensemblrs756912930
gopubmedrs756912930
geneviewrs756912930
scholarrs756912930
googlers756912930
pharmgkbrs756912930
gwascentralrs756912930
openSNPrs756912930
23andMers756912930
23andMe allrs756912930
SNP Nexus

SNPshotrs756912930
SNPdbers756912930
MSV3drs756912930
GWAS Ctlgrs756912930
Max Magnitude0
ClinVar
Risk rs756912930(A,C,T;A,C,T)
Alt rs756912930(A,C,T;A,C,T)
Reference rs756912930(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene APC
CLNDBN not specified not provided
Reversed 0
HGVS NC_000005.9:g.112175786G>A; NC_000005.9:g.112175786G>T
CLNSRC
CLNACC RCV000235790.1, RCV000202036.1,