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rs1064795688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome5
Position112841163
GeneAPC
is asnp
is mentioned by
dbSNPrs1064795688
dbSNP (classic)rs1064795688
ClinGenrs1064795688
ebirs1064795688
HLIrs1064795688
Exacrs1064795688
Gnomadrs1064795688
Varsomers1064795688
LitVarrs1064795688
Maprs1064795688
PheGenIrs1064795688
Biobankrs1064795688
1000 genomesrs1064795688
hgdprs1064795688
ensemblrs1064795688
geneviewrs1064795688
scholarrs1064795688
googlers1064795688
pharmgkbrs1064795688
gwascentralrs1064795688
openSNPrs1064795688
23andMers1064795688
23andMe allrs1064795688
SNPshotrs1064795688
SNPdbers1064795688
MSV3drs1064795688
GWAS Ctlgrs1064795688
Max Magnitude0
ClinVar
Risk rs1064795688(-;-)
Alt rs1064795688(-;-)
Reference Rs1064795688(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112176860delT
CLNSRC
CLNACC RCV000487142.1,