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

rs587781196

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781196(C;T)
Make rs587781196(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position25370913
GeneUBE3A
is asnp
is mentioned by
dbSNPrs587781196
ebirs587781196
HLIrs587781196
Exacrs587781196
Varsomers587781196
Maprs587781196
PheGenIrs587781196
hapmaprs587781196
1000 genomesrs587781196
hgdprs587781196
ensemblrs587781196
gopubmedrs587781196
geneviewrs587781196
scholarrs587781196
googlers587781196
pharmgkbrs587781196
gwascentralrs587781196
openSNPrs587781196
23andMers587781196
23andMe allrs587781196
SNP Nexus

SNPshotrs587781196
SNPdbers587781196
MSV3drs587781196
GWAS Ctlgrs587781196
Max Magnitude0
ClinVar
Risk rs587781196(T;T)
Alt rs587781196(T;T)
Reference rs587781196(C;C)
Significance Pathogenic
Disease Angelman syndrome
Variation info
Gene UBE3A
CLNDBN Angelman syndrome
Reversed 1
HGVS NC_000015.9:g.25616060G>A
CLNSRC
CLNACC RCV000144270.1,