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rs587783097

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783097(C;T)
Make rs587783097(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position25339193
GeneUBE3A
is asnp
is mentioned by
dbSNPrs587783097
ebirs587783097
HLIrs587783097
Exacrs587783097
Varsomers587783097
Maprs587783097
PheGenIrs587783097
hapmaprs587783097
1000 genomesrs587783097
hgdprs587783097
ensemblrs587783097
gopubmedrs587783097
geneviewrs587783097
scholarrs587783097
googlers587783097
pharmgkbrs587783097
gwascentralrs587783097
openSNPrs587783097
23andMers587783097
23andMe allrs587783097
SNP Nexus

SNPshotrs587783097
SNPdbers587783097
MSV3drs587783097
GWAS Ctlgrs587783097
Max Magnitude0
ClinVar
Risk rs587783097(T;T)
Alt rs587783097(T;T)
Reference rs587783097(C;C)
Significance Probable-Pathogenic
Disease not provided Angelman syndrome
Variation info
Gene UBE3A
CLNDBN not provided Angelman syndrome
Reversed 1
HGVS NC_000015.9:g.25584340G>A
CLNSRC
CLNACC RCV000144763.1, RCV000147882.1,