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rs869312766

From SNPedia

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Geno Mag Summary
(TGAA;TGAA) 0 common in clinvar
Make rs869312766(-;-)
Make rs869312766(-;TGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position138783266
GeneCTNNA1
is asnp
is mentioned by
dbSNPrs869312766
ebirs869312766
HLIrs869312766
Exacrs869312766
Varsomers869312766
Maprs869312766
PheGenIrs869312766
hapmaprs869312766
1000 genomesrs869312766
hgdprs869312766
ensemblrs869312766
gopubmedrs869312766
geneviewrs869312766
scholarrs869312766
googlers869312766
pharmgkbrs869312766
gwascentralrs869312766
openSNPrs869312766
23andMers869312766
23andMe allrs869312766
SNP Nexus

SNPshotrs869312766
SNPdbers869312766
MSV3drs869312766
GWAS Ctlgrs869312766
Max Magnitude0
ClinVar
Risk rs869312766(;)
Alt rs869312766(;)
Reference rs869312766(TGAA;TGAA)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CTNNA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.138118955_138118958delTGAA
CLNSRC
CLNACC RCV000210185.1,