rs139590686

Orientation

plus

Stabilized

plus

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

Make rs139590686(G;G)

Make rs139590686(G;T)

Reference

GRCh38.p7 38.3/149

Chromosome

15

Position

89321007

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs139590686
dbSNP (classic)	rs139590686
ClinGen	rs139590686
ebi	rs139590686
HLI	rs139590686
Exac	rs139590686
Gnomad	rs139590686
Varsome	rs139590686
LitVar	rs139590686
Map	rs139590686
PheGenI	rs139590686
Biobank	rs139590686
1000 genomes	rs139590686
hgdp	rs139590686
ensembl	rs139590686
geneview	rs139590686
scholar	rs139590686
google	rs139590686
pharmgkb	rs139590686
gwascentral	rs139590686
openSNP	rs139590686
23andMe	rs139590686
SNPshot	rs139590686
SNPdbe	rs139590686
MSV3d	rs139590686
GWAS Ctlg	rs139590686

Max Magnitude

0

ClinVar
Risk	rs139590686(G;G)
Alt	rs139590686(G;G)
Reference	Rs139590686(T;T)
Significance	Pathogenic
Disease	POLG-Related Spectrum Disorders not provided
Variation	info
Gene	POLG
CLNDBN	POLG-Related Spectrum Disorders not provided
Reversed	0
HGVS	NC_000015.9:g.89864238T>G
CLNSRC	Illumina
CLNACC	RCV000306622.1, RCV000321917.2,