Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
Evidence status

Synonyms

Archive dbSNP rs59522690

HGVS names

This variant has 2 HGVS names - Hide

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

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

Variant displays