Variant: rs28834970

Variant information

Location
8:27337604
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
-
Minor allele
-
MAF
-
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations

Variant and
risk allele
P-value P-value
annotation
RAF OR Beta CI Mapped gene Reported trait Trait(s) Background
trait(s)
Study accession First Author PubMed ID Location