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rs1064795802

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome13
Position52024665
GeneALG11, UTP14C
is asnp
is mentioned by
dbSNPrs1064795802
dbSNP (old)rs1064795802
ClinGenrs1064795802
ebirs1064795802
HLIrs1064795802
Exacrs1064795802
Gnomadrs1064795802
Varsomers1064795802
Maprs1064795802
PheGenIrs1064795802
Biobankrs1064795802
1000 genomesrs1064795802
hgdprs1064795802
ensemblrs1064795802
gopubmedrs1064795802
geneviewrs1064795802
scholarrs1064795802
googlers1064795802
pharmgkbrs1064795802
gwascentralrs1064795802
openSNPrs1064795802
23andMers1064795802
23andMe allrs1064795802
SNPshotrs1064795802
SNPdbers1064795802
MSV3drs1064795802
GWAS Ctlgrs1064795802
Max Magnitude0
ClinVar
Risk rs1064795802(G;G)
Alt rs1064795802(G;G)
Reference Rs1064795802(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALG11 UTP14C
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.52598801A>G
CLNSRC
CLNACC RCV000485363.1,