Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.25 (A)
Location

Chromosome 17:17229304 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs3890038

This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts and has 2512 individual genotypes.

Variation displays