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rs1057520556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520556(A;T)
Make rs1057520556(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41225766
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1057520556
dbSNP (old)rs1057520556
ClinGenrs1057520556
ebirs1057520556
HLIrs1057520556
Exacrs1057520556
Gnomadrs1057520556
Varsomers1057520556
Maprs1057520556
PheGenIrs1057520556
Biobankrs1057520556
1000 genomesrs1057520556
hgdprs1057520556
ensemblrs1057520556
gopubmedrs1057520556
geneviewrs1057520556
scholarrs1057520556
googlers1057520556
pharmgkbrs1057520556
gwascentralrs1057520556
openSNPrs1057520556
23andMers1057520556
23andMe allrs1057520556
SNPshotrs1057520556
SNPdbers1057520556
MSV3drs1057520556
GWAS Ctlgrs1057520556
Max Magnitude0
ClinVar
Risk rs1057520556(T;T)
Alt rs1057520556(T;T)
Reference Rs1057520556(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41267257A>T
CLNSRC
CLNACC RCV000422243.1,