Original source

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

Alleles
-/C
Location

Chromosome X: between 83506303 and 83506304 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts.

Variation displays