Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 3:87262138 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM066184

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_150_POU1F1_173110_0015, 4701

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

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays