Original source

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

C/A | Ancestral: C | Ambiguity code: M

Chromosome 6:111605452 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 7 transcripts and 1 regulatory feature.

Variant displays