Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 3:87264323 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961137

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4693, 2010_April_001_144_POU1F1_173110_0007

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

Variation displays