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rs1064795792

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome5
Position112835069
GeneAPC
is asnp
is mentioned by
dbSNPrs1064795792
dbSNP (old)rs1064795792
ClinGenrs1064795792
ebirs1064795792
HLIrs1064795792
Exacrs1064795792
Gnomadrs1064795792
Varsomers1064795792
Maprs1064795792
PheGenIrs1064795792
Biobankrs1064795792
1000 genomesrs1064795792
hgdprs1064795792
ensemblrs1064795792
gopubmedrs1064795792
geneviewrs1064795792
scholarrs1064795792
googlers1064795792
pharmgkbrs1064795792
gwascentralrs1064795792
openSNPrs1064795792
23andMers1064795792
23andMe allrs1064795792
SNPshotrs1064795792
SNPdbers1064795792
MSV3drs1064795792
GWAS Ctlgrs1064795792
Max Magnitude0
ClinVar
Risk rs1064795792(-;-)
Alt rs1064795792(-;-)
Reference Rs1064795792(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112170766delC
CLNSRC
CLNACC RCV000479266.1,