rs796052890

Orientation

minus

Stabilized

minus

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

Make rs796052890(A;A)

Make rs796052890(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89320998

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs796052890
dbSNP (classic)	rs796052890
ClinGen	rs796052890
ebi	rs796052890
HLI	rs796052890
Exac	rs796052890
Gnomad	rs796052890
Varsome	rs796052890
LitVar	rs796052890
Map	rs796052890
PheGenI	rs796052890
Biobank	rs796052890
1000 genomes	rs796052890
hgdp	rs796052890
ensembl	rs796052890
geneview	rs796052890
scholar	rs796052890
google	rs796052890
pharmgkb	rs796052890
gwascentral	rs796052890
openSNP	rs796052890
23andMe	rs796052890
SNPshot	rs796052890
SNPdbe	rs796052890
MSV3d	rs796052890
GWAS Ctlg	rs796052890

Max Magnitude

0

ClinVar
Risk	rs796052890(A;A)
Alt	rs796052890(A;A)
Reference	Rs796052890(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	POLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.89864229C>T
CLNSRC
CLNACC	RCV000188587.1,