rs796052908

Orientation

minus

Stabilized

minus

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

Make rs796052908(-;-)

Make rs796052908(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89327329

Gene	MIR6766, POLG

is a	snp
is	mentioned by
dbSNP	rs796052908
dbSNP (classic)	rs796052908
ClinGen	rs796052908
ebi	rs796052908
HLI	rs796052908
Exac	rs796052908
Gnomad	rs796052908
Varsome	rs796052908
LitVar	rs796052908
Map	rs796052908
PheGenI	rs796052908
Biobank	rs796052908
1000 genomes	rs796052908
hgdp	rs796052908
ensembl	rs796052908
geneview	rs796052908
scholar	rs796052908
google	rs796052908
pharmgkb	rs796052908
gwascentral	rs796052908
openSNP	rs796052908
23andMe	rs796052908
SNPshot	rs796052908
SNPdbe	rs796052908
MSV3d	rs796052908
GWAS Ctlg	rs796052908

Max Magnitude

0

ClinVar
Risk	rs796052908(-;-)
Alt	rs796052908(-;-)
Reference	Rs796052908(CT;CT)
Significance	Pathogenic
Disease	not provided Generalized epilepsy Global developmental delay Obesity
Variation	info
Gene	MIR6766 POLG
CLNDBN	not provided Generalized epilepsy Global developmental delay Obesity
Reversed	1
HGVS	NC_000015.9:g.89870560_89870561delAG
CLNSRC
CLNACC	RCV000188674.2, RCV000449589.1,