Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 3:87262161 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920589

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4687, 2010_April_001_138_POU1F1_173110_0001

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

Variation displays