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rs1064795803

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome13
Position52028334
GeneALG11, UTP14C
is asnp
is mentioned by
dbSNPrs1064795803
dbSNP (old)rs1064795803
ClinGenrs1064795803
ebirs1064795803
HLIrs1064795803
Exacrs1064795803
Gnomadrs1064795803
Varsomers1064795803
LitVarrs1064795803
Maprs1064795803
PheGenIrs1064795803
Biobankrs1064795803
1000 genomesrs1064795803
hgdprs1064795803
ensemblrs1064795803
gopubmedrs1064795803
geneviewrs1064795803
scholarrs1064795803
googlers1064795803
pharmgkbrs1064795803
gwascentralrs1064795803
openSNPrs1064795803
23andMers1064795803
23andMe allrs1064795803
SNPshotrs1064795803
SNPdbers1064795803
MSV3drs1064795803
GWAS Ctlgrs1064795803
Max Magnitude0
ClinVar
Risk rs1064795803(G;G)
Alt rs1064795803(G;G)
Reference Rs1064795803(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALG11 UTP14C
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.52602470T>G
CLNSRC
CLNACC RCV000480080.1,