Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/T | Ancestral: A | Ambiguity code: D | MAF: 0.02 (A)

Chromosome 8:39919023 (forward strand) | View in location tab


with HGMD-PUBLIC CS113011

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 22 transcripts, has 2758 sample genotypes and is mentioned in 1 citation.

Variant displays