rs796052916

Orientation

minus

Stabilized

minus

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

Make rs796052916(A;G)

Make rs796052916(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89328795

Gene	MIR6766, POLG

is a	snp
is	mentioned by
dbSNP	rs796052916
dbSNP (classic)	rs796052916
ClinGen	rs796052916
ebi	rs796052916
HLI	rs796052916
Exac	rs796052916
Gnomad	rs796052916
Varsome	rs796052916
LitVar	rs796052916
Map	rs796052916
PheGenI	rs796052916
Biobank	rs796052916
1000 genomes	rs796052916
hgdp	rs796052916
ensembl	rs796052916
geneview	rs796052916
scholar	rs796052916
google	rs796052916
pharmgkb	rs796052916
gwascentral	rs796052916
openSNP	rs796052916
23andMe	rs796052916
SNPshot	rs796052916
SNPdbe	rs796052916
MSV3d	rs796052916
GWAS Ctlg	rs796052916

Max Magnitude

0

ClinVar
Risk	rs796052916(G;G)
Alt	rs796052916(G;G)
Reference	Rs796052916(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MIR6766 POLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.89872026T>C
CLNSRC
CLNACC	RCV000188692.2,