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rs1064796494

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome5
Position11384946
GeneCTNND2
is asnp
is mentioned by
dbSNPrs1064796494
dbSNP (old)rs1064796494
ClinGenrs1064796494
ebirs1064796494
HLIrs1064796494
Exacrs1064796494
Gnomadrs1064796494
Varsomers1064796494
Maprs1064796494
PheGenIrs1064796494
Biobankrs1064796494
1000 genomesrs1064796494
hgdprs1064796494
ensemblrs1064796494
gopubmedrs1064796494
geneviewrs1064796494
scholarrs1064796494
googlers1064796494
pharmgkbrs1064796494
gwascentralrs1064796494
openSNPrs1064796494
23andMers1064796494
23andMe allrs1064796494
SNPshotrs1064796494
SNPdbers1064796494
MSV3drs1064796494
GWAS Ctlgrs1064796494
Max Magnitude0
ClinVar
Risk rs1064796494(A;A)
Alt rs1064796494(A;A)
Reference Rs1064796494(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTNND2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.11385058G>T
CLNSRC
CLNACC RCV000485964.1,