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
Synonyms

Archive dbSNP rs72149965

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

About this variant

This variant overlaps 33 transcripts.

Variation displays