Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome X:48898806 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs72149965

This variant has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 32 transcripts and 1 regulatory feature.

Variant displays