Original source

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

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

Chromosome X:38352697 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062983, CM971091

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Variation displays