rs5744760

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common/normal
(A;G)	1	Likely benign variant

Make rs5744760(G;G)

Reference

GRCh38.p7 38.3/151

Chromosome

12

Position

132676107

Gene

POLE

is a	snp
is	mentioned by
dbSNP	rs5744760
dbSNP (classic)	rs5744760
ClinGen	rs5744760
ebi	rs5744760
HLI	rs5744760
Exac	rs5744760
Gnomad	rs5744760
Varsome	rs5744760
LitVar	rs5744760
Map	rs5744760
PheGenI	rs5744760
Biobank	rs5744760
1000 genomes	rs5744760
hgdp	rs5744760
ensembl	rs5744760
geneview	rs5744760
scholar	rs5744760
google	rs5744760
pharmgkb	rs5744760
gwascentral	rs5744760
openSNP	rs5744760
23andMe	rs5744760
SNPshot	rs5744760
SNPdbe	rs5744760
MSV3d	rs5744760
GWAS Ctlg	rs5744760

Max Magnitude

1

c.1007A>G, p.Asn336Ser

?	(A;A) (A;G) (G;G)	28

ClinVar consensus is that this variant, rs5744760(G), is likely to be benign.