Original source

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

Alleles
T/A/G|Ancestral: T|Ambiguity code: D
Location

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

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 8 HGVS names - 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