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rs786205621

From SNPedia

Orientationplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs786205621(-;-)
Make rs786205621(-;CTC)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position109509662
GeneUBE3B
is asnp
is mentioned by
dbSNPrs786205621
ebirs786205621
HLIrs786205621
Exacrs786205621
Varsomers786205621
Maprs786205621
PheGenIrs786205621
hapmaprs786205621
1000 genomesrs786205621
hgdprs786205621
ensemblrs786205621
gopubmedrs786205621
geneviewrs786205621
scholarrs786205621
googlers786205621
pharmgkbrs786205621
gwascentralrs786205621
openSNPrs786205621
23andMers786205621
23andMe allrs786205621
SNP Nexus

SNPshotrs786205621
SNPdbers786205621
MSV3drs786205621
GWAS Ctlgrs786205621
Max Magnitude0
ClinVar
Risk rs786205621(;)
Alt rs786205621(;)
Reference rs786205621(CTC;CTC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene UBE3B
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.109947467_109947469delCTC
CLNSRC
CLNACC RCV000171471.1,