rs138929605

Orientation

plus

Stabilized

plus

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

Make rs138929605(A;A)

Make rs138929605(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89330106

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs138929605
dbSNP (classic)	rs138929605
ClinGen	rs138929605
ebi	rs138929605
HLI	rs138929605
Exac	rs138929605
Gnomad	rs138929605
Varsome	rs138929605
LitVar	rs138929605
Map	rs138929605
PheGenI	rs138929605
Biobank	rs138929605
1000 genomes	rs138929605
hgdp	rs138929605
ensembl	rs138929605
geneview	rs138929605
scholar	rs138929605
google	rs138929605
pharmgkb	rs138929605
gwascentral	rs138929605
openSNP	rs138929605
23andMe	rs138929605
SNPshot	rs138929605
SNPdbe	rs138929605
MSV3d	rs138929605
GWAS Ctlg	rs138929605

Max Magnitude

0

ClinVar
Risk	rs138929605(A;A) rs138929605(C;C)
Alt	rs138929605(A;A) rs138929605(C;C)
Reference	Rs138929605(T;T)
Significance	Probable-Pathogenic
Disease	not provided Progressive sclerosing poliodystrophy POLG-Related Spectrum Disorders
Variation	info
Gene	POLG
CLNDBN	not provided Progressive sclerosing poliodystrophy POLG-Related Spectrum Disorders
Reversed	0
HGVS	NC_000015.9:g.89873337T>A
CLNSRC
CLNACC	RCV000188643.2, RCV000231645.2, RCV000396333.1,