rs146639652

Orientation

plus

Stabilized

plus

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

Make rs146639652(A;A)

Make rs146639652(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

132675752

Gene

POLE

is a	snp
is	mentioned by
dbSNP	rs146639652
dbSNP (classic)	rs146639652
ClinGen	rs146639652
ebi	rs146639652
HLI	rs146639652
Exac	rs146639652
Gnomad	rs146639652
Varsome	rs146639652
LitVar	rs146639652
Map	rs146639652
PheGenI	rs146639652
Biobank	rs146639652
1000 genomes	rs146639652
hgdp	rs146639652
ensembl	rs146639652
geneview	rs146639652
scholar	rs146639652
google	rs146639652
pharmgkb	rs146639652
gwascentral	rs146639652
openSNP	rs146639652
23andMe	rs146639652
SNPshot	rs146639652
SNPdbe	rs146639652
MSV3d	rs146639652
GWAS Ctlg	rs146639652

Max Magnitude

0

ClinVar
Risk	rs146639652(A;A) rs146639652(C;C)
Alt	rs146639652(A;A) rs146639652(C;C)
Reference	Rs146639652(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	POLE
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000012.11:g.133252338G>A; NC_000012.11:g.133252338G>C
CLNSRC
CLNACC	RCV000430369.1, RCV000485372.1,