Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance

Synonyms

LSDB 4697, 2010_April_001_147_POU1F1_173110_0011

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

Variation displays