rs2953983
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2953983(C;C) |
Make rs2953983(C;T) |
Make rs2953983(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 42355738 |
Gene | POLB |
is a | snp |
is | mentioned by |
dbSNP | rs2953983 |
dbSNP (classic) | rs2953983 |
ClinGen | rs2953983 |
ebi | rs2953983 |
HLI | rs2953983 |
Exac | rs2953983 |
Gnomad | rs2953983 |
Varsome | rs2953983 |
LitVar | rs2953983 |
Map | rs2953983 |
PheGenI | rs2953983 |
Biobank | rs2953983 |
1000 genomes | rs2953983 |
hgdp | rs2953983 |
ensembl | rs2953983 |
geneview | rs2953983 |
scholar | rs2953983 |
rs2953983 | |
pharmgkb | rs2953983 |
gwascentral | rs2953983 |
openSNP | rs2953983 |
23andMe | rs2953983 |
SNPshot | rs2953983 |
SNPdbe | rs2953983 |
MSV3d | rs2953983 |
GWAS Ctlg | rs2953983 |
GMAF | 0.2433 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22406557] Human longevity and variation in GH/IGF-1/insulin signaling, DNA damage signaling and repair and pro/antioxidant pathway genes: Cross sectional and longitudinal studies.
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.
[PMID 18778477] Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.
[PMID 19167932] Population-specific variation in haplotype composition and heterozygosity at the POLB locus.