Original source

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

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

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

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

Synonyms

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