Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 3:87260082 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021317

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 4698, 2010_April_001_148_POU1F1_173110_0012

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, 2 regulatory features and is associated with 2 phenotypes.

Variant displays