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rs1057521882

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521882(C;C)
Make rs1057521882(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41239133
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1057521882
dbSNP (old)rs1057521882
ClinGenrs1057521882
ebirs1057521882
HLIrs1057521882
Exacrs1057521882
Gnomadrs1057521882
Varsomers1057521882
Maprs1057521882
PheGenIrs1057521882
Biobankrs1057521882
1000 genomesrs1057521882
hgdprs1057521882
ensemblrs1057521882
gopubmedrs1057521882
geneviewrs1057521882
scholarrs1057521882
googlers1057521882
pharmgkbrs1057521882
gwascentralrs1057521882
openSNPrs1057521882
23andMers1057521882
23andMe allrs1057521882
SNPshotrs1057521882
SNPdbers1057521882
MSV3drs1057521882
GWAS Ctlgrs1057521882
Max Magnitude0
ClinVar
Risk rs1057521882(C;C)
Alt rs1057521882(C;C)
Reference Rs1057521882(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41280624G>C
CLNSRC
CLNACC RCV000443498.1,