rs57875989

Orientation

plus

Stabilized

plus

Make rs57875989(-;-)

Make rs57875989(-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC)

Make rs57875989(GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC)

Reference

GRCh38 38.1/141

Chromosome

1

Position

7829993

Gene

PER3

is a	snp
is	mentioned by
dbSNP	rs57875989
dbSNP (classic)	rs57875989
ClinGen	rs57875989
ebi	rs57875989
HLI	rs57875989
Exac	rs57875989
Gnomad	rs57875989
Varsome	rs57875989
LitVar	rs57875989
Map	rs57875989
PheGenI	rs57875989
Biobank	rs57875989
1000 genomes	rs57875989
hgdp	rs57875989
ensembl	rs57875989
geneview	rs57875989
scholar	rs57875989
google	rs57875989
pharmgkb	rs57875989
gwascentral	rs57875989
openSNP	rs57875989
23andMe	rs57875989
SNPshot	rs57875989
SNPdbe	rs57875989
MSV3d	rs57875989
GWAS Ctlg	rs57875989

Max Magnitude

0

[PMID 24860629] Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian Sample

[PMID 24866331] Period3 VNTR polymorphism influences the time-of-day pain onset of acute myocardial infarction with ST elevation

[PMID 24892753] PER2 rs2304672, CLOCK rs1801260, and PER3 rs57875989 polymorphisms are not associated with juvenile myoclonic epilepsy

[PMID 25798540] Differences in planning performance, a neurocognitive endophenotype, are associated with a functional variant in PER3 gene