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

rs587781201

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781201(A;A)
Make rs587781201(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position25370743
GeneUBE3A
is asnp
is mentioned by
dbSNPrs587781201
ebirs587781201
HLIrs587781201
Exacrs587781201
Varsomers587781201
Maprs587781201
PheGenIrs587781201
hapmaprs587781201
1000 genomesrs587781201
hgdprs587781201
ensemblrs587781201
gopubmedrs587781201
geneviewrs587781201
scholarrs587781201
googlers587781201
pharmgkbrs587781201
gwascentralrs587781201
openSNPrs587781201
23andMers587781201
23andMe allrs587781201
SNP Nexus

SNPshotrs587781201
SNPdbers587781201
MSV3drs587781201
GWAS Ctlgrs587781201
Max Magnitude0
ClinVar
Risk rs587781201(A;A)
Alt rs587781201(A;A)
Reference rs587781201(T;T)
Significance Pathogenic
Disease Angelman syndrome
Variation info
Gene UBE3A
CLNDBN Angelman syndrome
Reversed 1
HGVS NC_000015.9:g.25615890A>T
CLNSRC
CLNACC RCV000144275.1,