rs181860632

Orientation

plus

Stabilized

plus

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

Make rs181860632(A;A)

Make rs181860632(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

89319065

Gene

POLG

is a	snp
is	mentioned by
dbSNP	rs181860632
dbSNP (classic)	rs181860632
ClinGen	rs181860632
ebi	rs181860632
HLI	rs181860632
Exac	rs181860632
Gnomad	rs181860632
Varsome	rs181860632
LitVar	rs181860632
Map	rs181860632
PheGenI	rs181860632
Biobank	rs181860632
1000 genomes	rs181860632
hgdp	rs181860632
ensembl	rs181860632
geneview	rs181860632
scholar	rs181860632
google	rs181860632
pharmgkb	rs181860632
gwascentral	rs181860632
openSNP	rs181860632
23andMe	rs181860632
SNPshot	rs181860632
SNPdbe	rs181860632
MSV3d	rs181860632
GWAS Ctlg	rs181860632

Max Magnitude

0

ClinVar
Risk	rs181860632(A;A)
Alt	rs181860632(A;A)
Reference	Rs181860632(G;G)
Significance	Other
Disease	not provided
Variation	info
Gene	POLG
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.89862296G>A
CLNSRC
CLNACC	RCV000188603.3,