Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H
Location

Chromosome 6:158170467 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant

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

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts and 1 regulatory feature.

Variant displays