Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variant

HGMD-PUBLIC CM950972

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 6737, 2010_April_001_312_POU3F4_300039_0005

HGVS names

This variant has 3 HGVS names - Show

About this variant

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

Variant displays