Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:153687254 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and 2 regulatory features.

Variant displays