Original source

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

Alleles
G/A/T | Ambiguity code: D
Location

Chromosome X:48542796 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941405, CM941406, CM961454

Most severe consequence
Clinical significance

Synonyms

LSDB 7270, 7269

This variation has 20 HGVS names - click the plus to show

Variation displays