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rs1057518120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518120(A;G)
Make rs1057518120(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position11397173
GeneCTNND2
is asnp
is mentioned by
dbSNPrs1057518120
dbSNP (old)rs1057518120
ClinGenrs1057518120
ebirs1057518120
HLIrs1057518120
Exacrs1057518120
Gnomadrs1057518120
Varsomers1057518120
LitVarrs1057518120
Maprs1057518120
PheGenIrs1057518120
Biobankrs1057518120
1000 genomesrs1057518120
hgdprs1057518120
ensemblrs1057518120
gopubmedrs1057518120
geneviewrs1057518120
scholarrs1057518120
googlers1057518120
pharmgkbrs1057518120
gwascentralrs1057518120
openSNPrs1057518120
23andMers1057518120
23andMe allrs1057518120
SNPshotrs1057518120
SNPdbers1057518120
MSV3drs1057518120
GWAS Ctlgrs1057518120
Max Magnitude0
ClinVar
Risk rs1057518120(G;G)
Alt rs1057518120(G;G)
Reference Rs1057518120(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CTNND2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.11397285T>C
CLNSRC
CLNACC RCV000413978.1,