Original source

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

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

Chromosome X:153687224 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

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

About this variant

This variant overlaps 15 transcripts and 2 regulatory features.

Variant displays