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rs483352717

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483352717(A;A)
Make rs483352717(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position41225561
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs483352717
ebirs483352717
HLIrs483352717
Exacrs483352717
Varsomers483352717
Maprs483352717
PheGenIrs483352717
hapmaprs483352717
1000 genomesrs483352717
hgdprs483352717
ensemblrs483352717
gopubmedrs483352717
geneviewrs483352717
scholarrs483352717
googlers483352717
pharmgkbrs483352717
gwascentralrs483352717
openSNPrs483352717
23andMers483352717
23andMe allrs483352717
SNP Nexus

SNPshotrs483352717
SNPdbers483352717
MSV3drs483352717
GWAS Ctlgrs483352717
Max Magnitude0
ClinVar
Risk rs483352717(A;A)
Alt rs483352717(A;A)
Reference rs483352717(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41267052G>A
CLNSRC
CLNACC RCV000087198.2,