Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/T | MAF: < 0.01 (-)
Location

Chromosome 22: between 23252624 and 23252625 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2513 sample genotypes.

Variant displays