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rs1064796646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position41234302
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1064796646
dbSNP (old)rs1064796646
ClinGenrs1064796646
ebirs1064796646
HLIrs1064796646
Exacrs1064796646
Gnomadrs1064796646
Varsomers1064796646
LitVarrs1064796646
Maprs1064796646
PheGenIrs1064796646
Biobankrs1064796646
1000 genomesrs1064796646
hgdprs1064796646
ensemblrs1064796646
gopubmedrs1064796646
geneviewrs1064796646
scholarrs1064796646
googlers1064796646
pharmgkbrs1064796646
gwascentralrs1064796646
openSNPrs1064796646
23andMers1064796646
23andMe allrs1064796646
SNPshotrs1064796646
SNPdbers1064796646
MSV3drs1064796646
GWAS Ctlgrs1064796646
Max Magnitude0
ClinVar
Risk rs1064796646(C;C)
Alt rs1064796646(C;C)
Reference Rs1064796646(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41275793G>C
CLNSRC
CLNACC RCV000478309.1,