Original source

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

Alleles
A/-
Location

Chromosome 12:52287337 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and 2 regulatory features.

Variant displays