Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome X:83508928 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950969

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6735, 2010_April_001_310_POU3F4_300039_0003

This variation has 4 HGVS names - click the plus to show

Variation displays