Original source

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

T/A | Ancestral: A | Ambiguity code: W | MAF: 0.42 (T)

Chromosome 22:35068980 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts and has 4039 sample genotypes.

Variant displays