Original source

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

Archive dbSNP rs60463436

This variant has 4 HGVS names - click the plus to show

About this variant

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

Variant displays