Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520730

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520730(A;A)
Make rs1057520730(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41234194
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1057520730
dbSNP (old)rs1057520730
ClinGenrs1057520730
ebirs1057520730
HLIrs1057520730
Exacrs1057520730
Gnomadrs1057520730
Varsomers1057520730
Maprs1057520730
PheGenIrs1057520730
Biobankrs1057520730
1000 genomesrs1057520730
hgdprs1057520730
ensemblrs1057520730
gopubmedrs1057520730
geneviewrs1057520730
scholarrs1057520730
googlers1057520730
pharmgkbrs1057520730
gwascentralrs1057520730
openSNPrs1057520730
23andMers1057520730
23andMe allrs1057520730
SNPshotrs1057520730
SNPdbers1057520730
MSV3drs1057520730
GWAS Ctlgrs1057520730
Max Magnitude0
ClinVar
Risk rs1057520730(A;A)
Alt rs1057520730(A;A)
Reference Rs1057520730(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41275685T>A
CLNSRC
CLNACC RCV000442337.1,