Original source

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

Clinical significance

This variant has 3 synonyms - click the plus to show

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

About this variant

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

Variant displays