Original source

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

Alleles
-/AA
Location

Chromosome 1: between 225409160 and 225409161 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays