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rs1064794465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Chromosome13
Position52024716
GeneALG11, UTP14C
is asnp
is mentioned by
dbSNPrs1064794465
dbSNP (classic)rs1064794465
ClinGenrs1064794465
ebirs1064794465
HLIrs1064794465
Exacrs1064794465
Gnomadrs1064794465
Varsomers1064794465
LitVarrs1064794465
Maprs1064794465
PheGenIrs1064794465
Biobankrs1064794465
1000 genomesrs1064794465
hgdprs1064794465
ensemblrs1064794465
geneviewrs1064794465
scholarrs1064794465
googlers1064794465
pharmgkbrs1064794465
gwascentralrs1064794465
openSNPrs1064794465
23andMers1064794465
23andMe allrs1064794465
SNPshotrs1064794465
SNPdbers1064794465
MSV3drs1064794465
GWAS Ctlgrs1064794465
Max Magnitude0
ClinVar
Risk rs1064794465(-;-)
Alt rs1064794465(-;-)
Reference Rs1064794465(AAG;AAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALG11 UTP14C
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.52598852_52598854delAGA
CLNSRC
CLNACC RCV000484706.1,