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rs1064796757

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome11
Position72402994
GeneCLPB
is asnp
is mentioned by
dbSNPrs1064796757
dbSNP (old)rs1064796757
ClinGenrs1064796757
ebirs1064796757
HLIrs1064796757
Exacrs1064796757
Gnomadrs1064796757
Varsomers1064796757
Maprs1064796757
PheGenIrs1064796757
Biobankrs1064796757
1000 genomesrs1064796757
hgdprs1064796757
ensemblrs1064796757
gopubmedrs1064796757
geneviewrs1064796757
scholarrs1064796757
googlers1064796757
pharmgkbrs1064796757
gwascentralrs1064796757
openSNPrs1064796757
23andMers1064796757
23andMe allrs1064796757
SNPshotrs1064796757
SNPdbers1064796757
MSV3drs1064796757
GWAS Ctlgrs1064796757
Max Magnitude0
ClinVar
Risk rs1064796757(C;C)
Alt rs1064796757(C;C)
Reference Rs1064796757(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLPB
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.72114038T>G
CLNSRC
CLNACC RCV000478888.1,