Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 22:50526717 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 20 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 32 transcripts and 1 regulatory feature.

Variant displays