Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:48386675 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002589

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6921, 2010_April_001_087_EBP_300205_0010

This variation has 5 HGVS names - click the plus to show

Variation displays