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rs864309577

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309577(C;T)
Make rs864309577(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position41236412
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs864309577
ebirs864309577
HLIrs864309577
Exacrs864309577
Varsomers864309577
Maprs864309577
PheGenIrs864309577
hapmaprs864309577
1000 genomesrs864309577
hgdprs864309577
ensemblrs864309577
gopubmedrs864309577
geneviewrs864309577
scholarrs864309577
googlers864309577
pharmgkbrs864309577
gwascentralrs864309577
openSNPrs864309577
23andMers864309577
23andMe allrs864309577
SNP Nexus

SNPshotrs864309577
SNPdbers864309577
MSV3drs864309577
GWAS Ctlgrs864309577
Max Magnitude0
ClinVar
Risk rs864309577(T;T)
Alt rs864309577(T;T)
Reference rs864309577(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CTNNB1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.41277903C>T
CLNSRC
CLNACC RCV000203130.1,