Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome X:18564539 (forward strand) | View in location tab

Co-located

with PhenCode RettBASE_c.145+17A>G (A/G)

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB 145+17A>G

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and is associated with 2 phenotypes.

Variant displays