Original source

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

Alleles
T/C/G | Ancestral: T | Ambiguity code: B
Location

Chromosome X:38367371 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062959, CM020166

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