Original source

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

Alleles
AA/-
Location

Chromosome 4:174511216-174511217 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 4 sample genotypes.

Variant displays