Original source

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

Alleles
-/G
Location

Chromosome X: between 83506268 and 83506269 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays