Original source

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

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

Chromosome X:48684407 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961454, CM941406, CM941405

Most severe consequence
Clinical significance

Synonyms

LSDB 7270, 7269

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

Variation displays