Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.48 (A)
Location

Chromosome 19:34817436 (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 rs59522690

This variation has 2 HGVS names - click the plus to show

19:g.34817436A>T
ENST00000590963.1:n.798T>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 2880 individual genotypes and is mentioned in 1 citation.

Variation displays