Original source

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

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

Chromosome X:82764332 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM950972

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6737, 2010_April_001_312_POU3F4_300039_0005

This variation has 3 HGVS names - click the plus to show

Variation displays