Original source

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

Alleles
-/AAT
Location

Chromosome X: between 151400348 and 151400349 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays