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rs587781244

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781244(A;A)
Make rs587781244(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position25356893
GeneUBE3A
is asnp
is mentioned by
dbSNPrs587781244
ebirs587781244
HLIrs587781244
Exacrs587781244
Varsomers587781244
Maprs587781244
PheGenIrs587781244
hapmaprs587781244
1000 genomesrs587781244
hgdprs587781244
ensemblrs587781244
gopubmedrs587781244
geneviewrs587781244
scholarrs587781244
googlers587781244
pharmgkbrs587781244
gwascentralrs587781244
openSNPrs587781244
23andMers587781244
23andMe allrs587781244
SNP Nexus

SNPshotrs587781244
SNPdbers587781244
MSV3drs587781244
GWAS Ctlgrs587781244
Max Magnitude0
ClinVar
Risk rs587781244(A;A)
Alt rs587781244(A;A)
Reference rs587781244(T;T)
Significance Probable-Pathogenic
Disease not specified Angelman syndrome
Variation info
Gene UBE3A
CLNDBN not specified Angelman syndrome
Reversed 1
HGVS NC_000015.9:g.25602040A>C; NC_000015.9:g.25602040A>T
CLNSRC
CLNACC RCV000201268.1, RCV000144321.1,