Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome X:153694424 (forward strand) | View in location tab

Co-located

with COSMIC COSM3235790 (C/T) ; HGMD-PUBLIC CM065469

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6721

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts and is associated with 2 phenotypes.

Variation displays