rs796052911

Orientation

minus

Stabilized

minus

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

Make rs796052911(C;C)

Make rs796052911(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89319031

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs796052911
dbSNP (classic)	rs796052911
ClinGen	rs796052911
ebi	rs796052911
HLI	rs796052911
Exac	rs796052911
Gnomad	rs796052911
Varsome	rs796052911
LitVar	rs796052911
Map	rs796052911
PheGenI	rs796052911
Biobank	rs796052911
1000 genomes	rs796052911
hgdp	rs796052911
ensembl	rs796052911
geneview	rs796052911
scholar	rs796052911
google	rs796052911
pharmgkb	rs796052911
gwascentral	rs796052911
openSNP	rs796052911
23andMe	rs796052911
SNPshot	rs796052911
SNPdbe	rs796052911
MSV3d	rs796052911
GWAS Ctlg	rs796052911

Max Magnitude

0

ClinVar
Risk	rs796052911(C;C)
Alt	rs796052911(C;C)
Reference	Rs796052911(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	POLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.89862262A>G
CLNSRC
CLNACC	RCV000188679.1,