Original source

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

Clinical significance

Synonyms

LSDB 2010_April_001_150_POU1F1_173110_0015, 4701

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

Variation displays