Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.02 (G)
Location

Chromosome 19:38620326 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 13 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts and has 2837 sample genotypes.

Variant displays