Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 3:87264294 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM024144

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 4697, 2010_April_001_147_POU1F1_173110_0011

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays