Original source

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

Alleles
AA/-
Location

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 4 sample genotypes.

Variant displays