rs796052891

Orientation

minus

Stabilized

minus

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

Make rs796052891(A;G)

Make rs796052891(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89320907

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs796052891
dbSNP (classic)	rs796052891
ClinGen	rs796052891
ebi	rs796052891
HLI	rs796052891
Exac	rs796052891
Gnomad	rs796052891
Varsome	rs796052891
LitVar	rs796052891
Map	rs796052891
PheGenI	rs796052891
Biobank	rs796052891
1000 genomes	rs796052891
hgdp	rs796052891
ensembl	rs796052891
geneview	rs796052891
scholar	rs796052891
google	rs796052891
pharmgkb	rs796052891
gwascentral	rs796052891
openSNP	rs796052891
23andMe	rs796052891
SNPshot	rs796052891
SNPdbe	rs796052891
MSV3d	rs796052891
GWAS Ctlg	rs796052891

Max Magnitude

0

ClinVar
Risk	rs796052891(G;G)
Alt	rs796052891(G;G)
Reference	Rs796052891(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	POLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.89864138T>C
CLNSRC
CLNACC	RCV000188590.2,