Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033596

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033596(A;C)
Make rs111033596(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position25371798
GeneUBE3A
is asnp
is mentioned by
dbSNPrs111033596
ebirs111033596
HLIrs111033596
Exacrs111033596
Varsomers111033596
Maprs111033596
PheGenIrs111033596
hapmaprs111033596
1000 genomesrs111033596
hgdprs111033596
ensemblrs111033596
gopubmedrs111033596
geneviewrs111033596
scholarrs111033596
googlers111033596
pharmgkbrs111033596
gwascentralrs111033596
openSNPrs111033596
23andMers111033596
23andMe allrs111033596
SNP Nexus

SNPshotrs111033596
SNPdbers111033596
MSV3drs111033596
GWAS Ctlgrs111033596
Max Magnitude0
OMIM601623
Desc
Variant0006
Relatedalso
ClinVar
Risk rs111033596(C;C)
Alt rs111033596(C;C)
Reference rs111033596(A;A)
Significance Pathogenic
Disease Angelman syndrome
Variation info
Gene UBE3A
CLNDBN Angelman syndrome
Reversed 1
HGVS NC_000015.9:g.25616945T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008432.2,