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rs775981553

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775981553(G;T)
Make rs775981553(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position109483612
GeneUBE3B
is asnp
is mentioned by
dbSNPrs775981553
ebirs775981553
HLIrs775981553
Exacrs775981553
Varsomers775981553
Maprs775981553
PheGenIrs775981553
hapmaprs775981553
1000 genomesrs775981553
hgdprs775981553
ensemblrs775981553
gopubmedrs775981553
geneviewrs775981553
scholarrs775981553
googlers775981553
pharmgkbrs775981553
gwascentralrs775981553
openSNPrs775981553
23andMers775981553
23andMe allrs775981553
SNP Nexus

SNPshotrs775981553
SNPdbers775981553
MSV3drs775981553
GWAS Ctlgrs775981553
Max Magnitude0
ClinVar
Risk rs775981553(T;T)
Alt rs775981553(T;T)
Reference rs775981553(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene UBE3B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000012.11:g.109921417G>T
CLNSRC
CLNACC RCV000210716.1,