Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome X:120426275 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

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

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays