Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:83509274 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950971

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_311_POU3F4_300039_0004, 6736

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