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rs797044875

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044875(A;A)
Make rs797044875(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position41235763
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs797044875
ebirs797044875
HLIrs797044875
Exacrs797044875
Varsomers797044875
Maprs797044875
PheGenIrs797044875
hapmaprs797044875
1000 genomesrs797044875
hgdprs797044875
ensemblrs797044875
gopubmedrs797044875
geneviewrs797044875
scholarrs797044875
googlers797044875
pharmgkbrs797044875
gwascentralrs797044875
openSNPrs797044875
23andMers797044875
23andMe allrs797044875
SNP Nexus

SNPshotrs797044875
SNPdbers797044875
MSV3drs797044875
GWAS Ctlgrs797044875
Max Magnitude0
ClinVar
Risk rs797044875(A;A)
Alt rs797044875(A;A)
Reference rs797044875(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CTNNB1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.41277254G>A
CLNSRC
CLNACC RCV000190686.1,