Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)
Location

Chromosome 8:89970586 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB Broad13929723

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 6 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays