Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:50085987 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960309

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000084.2:c.731C>T, 6622

This variation has 9 HGVS names - click the plus to show

Variation displays