rs786205621

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CTC;CTC)	0	common in clinvar

Make rs786205621(-;-)

Make rs786205621(-;CTC)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

109509662

Gene

UBE3B

is a	snp
is	mentioned by
dbSNP	rs786205621
dbSNP (classic)	rs786205621
ClinGen	rs786205621
ebi	rs786205621
HLI	rs786205621
Exac	rs786205621
Gnomad	rs786205621
Varsome	rs786205621
LitVar	rs786205621
Map	rs786205621
PheGenI	rs786205621
Biobank	rs786205621
1000 genomes	rs786205621
hgdp	rs786205621
ensembl	rs786205621
geneview	rs786205621
scholar	rs786205621
google	rs786205621
pharmgkb	rs786205621
gwascentral	rs786205621
openSNP	rs786205621
23andMe	rs786205621
SNPshot	rs786205621
SNPdbe	rs786205621
MSV3d	rs786205621
GWAS Ctlg	rs786205621

Max Magnitude

0

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,