Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome X:83509324 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950972

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 6737, 2010_April_001_312_POU3F4_300039_0005

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and is associated with 2 phenotypes.

Variant displays