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rs1064796453

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position41235799
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1064796453
dbSNP (old)rs1064796453
ClinGenrs1064796453
ebirs1064796453
HLIrs1064796453
Exacrs1064796453
Gnomadrs1064796453
Varsomers1064796453
Maprs1064796453
PheGenIrs1064796453
Biobankrs1064796453
1000 genomesrs1064796453
hgdprs1064796453
ensemblrs1064796453
gopubmedrs1064796453
geneviewrs1064796453
scholarrs1064796453
googlers1064796453
pharmgkbrs1064796453
gwascentralrs1064796453
openSNPrs1064796453
23andMers1064796453
23andMe allrs1064796453
SNPshotrs1064796453
SNPdbers1064796453
MSV3drs1064796453
GWAS Ctlgrs1064796453
Max Magnitude0
ClinVar
Risk rs1064796453(T;T)
Alt rs1064796453(T;T)
Reference Rs1064796453(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41277290C>T
CLNSRC
CLNACC RCV000486133.1,