Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
 
Missense variant
Evidence status

Clinical significance

Synonyms

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

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

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays