Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: G | Ambiguity code: R

Chromosome X:153688570 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and is associated with 1 phenotype.

Variant displays