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rs1064796961

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TCA;TCA) 0 common in clinvar
Chromosome11
Position72294105
GeneCLPB
is asnp
is mentioned by
dbSNPrs1064796961
dbSNP (old)rs1064796961
ClinGenrs1064796961
ebirs1064796961
HLIrs1064796961
Exacrs1064796961
Gnomadrs1064796961
Varsomers1064796961
Maprs1064796961
PheGenIrs1064796961
Biobankrs1064796961
1000 genomesrs1064796961
hgdprs1064796961
ensemblrs1064796961
gopubmedrs1064796961
geneviewrs1064796961
scholarrs1064796961
googlers1064796961
pharmgkbrs1064796961
gwascentralrs1064796961
openSNPrs1064796961
23andMers1064796961
23andMe allrs1064796961
SNPshotrs1064796961
SNPdbers1064796961
MSV3drs1064796961
GWAS Ctlgrs1064796961
Max Magnitude0
ClinVar
Risk rs1064796961(-;-)
Alt rs1064796961(-;-)
Reference Rs1064796961(TCA;TCA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLPB
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.72005149_72005151delTGA
CLNSRC
CLNACC RCV000483573.1,