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rs539407162

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs539407162(A;A)
Make rs539407162(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109533533
GeneUBE3B
is asnp
is mentioned by
dbSNPrs539407162
ebirs539407162
HLIrs539407162
Exacrs539407162
Varsomers539407162
Maprs539407162
PheGenIrs539407162
hapmaprs539407162
1000 genomesrs539407162
hgdprs539407162
ensemblrs539407162
gopubmedrs539407162
geneviewrs539407162
scholarrs539407162
googlers539407162
pharmgkbrs539407162
gwascentralrs539407162
openSNPrs539407162
23andMers539407162
23andMe allrs539407162
SNP Nexus

SNPshotrs539407162
SNPdbers539407162
MSV3drs539407162
GWAS Ctlgrs539407162
Max Magnitude0
ClinVar
Risk rs539407162(A;A)
Alt rs539407162(A;A)
Reference rs539407162(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene UBE3B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000012.11:g.109971338G>C
CLNSRC
CLNACC RCV000190746.1,