rs752892262

Orientation

plus

Stabilized

plus

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

Make rs752892262(A;A)

Make rs752892262(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89333267

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs752892262
dbSNP (classic)	rs752892262
ClinGen	rs752892262
ebi	rs752892262
HLI	rs752892262
Exac	rs752892262
Gnomad	rs752892262
Varsome	rs752892262
LitVar	rs752892262
Map	rs752892262
PheGenI	rs752892262
Biobank	rs752892262
1000 genomes	rs752892262
hgdp	rs752892262
ensembl	rs752892262
geneview	rs752892262
scholar	rs752892262
google	rs752892262
pharmgkb	rs752892262
gwascentral	rs752892262
openSNP	rs752892262
23andMe	rs752892262
SNPshot	rs752892262
SNPdbe	rs752892262
MSV3d	rs752892262
GWAS Ctlg	rs752892262

Max Magnitude

0

ClinVar
Risk	rs752892262(A;A)
Alt	rs752892262(A;A)
Reference	Rs752892262(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	POLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.89876498G>A
CLNSRC
CLNACC	RCV000188636.1,