rs796052892

Orientation

minus

Stabilized

minus

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

Make rs796052892(A;A)

Make rs796052892(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89319356

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs796052892
dbSNP (classic)	rs796052892
ClinGen	rs796052892
ebi	rs796052892
HLI	rs796052892
Exac	rs796052892
Gnomad	rs796052892
Varsome	rs796052892
LitVar	rs796052892
Map	rs796052892
PheGenI	rs796052892
Biobank	rs796052892
1000 genomes	rs796052892
hgdp	rs796052892
ensembl	rs796052892
geneview	rs796052892
scholar	rs796052892
google	rs796052892
pharmgkb	rs796052892
gwascentral	rs796052892
openSNP	rs796052892
23andMe	rs796052892
SNPshot	rs796052892
SNPdbe	rs796052892
MSV3d	rs796052892
GWAS Ctlg	rs796052892

Max Magnitude

0

ClinVar
Risk	rs796052892(A;A)
Alt	rs796052892(A;A)
Reference	Rs796052892(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	POLG
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.89862587G>T
CLNSRC
CLNACC	RCV000188596.1,