rs199759055

Orientation

plus

Stabilized

plus

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

Make rs199759055(A;A)

Make rs199759055(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89328699

Gene	MIR6766, POLG

is a	snp
is	mentioned by
dbSNP	rs199759055
dbSNP (classic)	rs199759055
ClinGen	rs199759055
ebi	rs199759055
HLI	rs199759055
Exac	rs199759055
Gnomad	rs199759055
Varsome	rs199759055
LitVar	rs199759055
Map	rs199759055
PheGenI	rs199759055
Biobank	rs199759055
1000 genomes	rs199759055
hgdp	rs199759055
ensembl	rs199759055
geneview	rs199759055
scholar	rs199759055
google	rs199759055
pharmgkb	rs199759055
gwascentral	rs199759055
openSNP	rs199759055
23andMe	rs199759055
SNPshot	rs199759055
SNPdbe	rs199759055
MSV3d	rs199759055
GWAS Ctlg	rs199759055

Max Magnitude

0

ClinVar
Risk	rs199759055(A;A)
Alt	rs199759055(A;A)
Reference	Rs199759055(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	MIR6766 POLG
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000015.9:g.89871930G>A
CLNSRC
CLNACC	RCV000188650.3, RCV000374911.1,