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rs587781191

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781191(C;T)
Make rs587781191(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position25371153
GeneUBE3A
is asnp
is mentioned by
dbSNPrs587781191
ebirs587781191
HLIrs587781191
Exacrs587781191
Varsomers587781191
Maprs587781191
PheGenIrs587781191
hapmaprs587781191
1000 genomesrs587781191
hgdprs587781191
ensemblrs587781191
gopubmedrs587781191
geneviewrs587781191
scholarrs587781191
googlers587781191
pharmgkbrs587781191
gwascentralrs587781191
openSNPrs587781191
23andMers587781191
23andMe allrs587781191
SNP Nexus

SNPshotrs587781191
SNPdbers587781191
MSV3drs587781191
GWAS Ctlgrs587781191
Max Magnitude0
ClinVar
Risk rs587781191(T;T)
Alt rs587781191(T;T)
Reference rs587781191(C;C)
Significance Pathogenic
Disease Angelman syndrome
Variation info
Gene UBE3A
CLNDBN Angelman syndrome
Reversed 1
HGVS NC_000015.9:g.25616300G>A
CLNSRC
CLNACC RCV000144265.1,