Original source

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

Alleles
-/T
Location

Chromosome X: between 48690989 and 48690990 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts.

Variant displays