Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome X:48684407 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961454, CM941406, CM941405

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7270, 7269

This variation has 20 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and is associated with 4 phenotypes.

Variation displays