Original source

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

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

Chromosome X:38367361 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920533, CM971095

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 10 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 6 transcripts, is associated with 4 phenotypes and is mentioned in 2 citations.

Variant displays