Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.02 (A)
Location

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

Co-located

with HGMD-PUBLIC CS113011

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays