Original source

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

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

Chromosome X:38212027 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS063356, CS971834

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

Variation displays