Original source

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

TTTG/- | MAF: 0.02 (-)

Chromosome 22:33276286-33276289 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2504 sample genotypes.

Variant displays