Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome X:38297424 (forward strand) | View in location tab

Co-located

with PhenCode RISN_RPGR:c.1274G>A (C/T), RPGR_00212 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2 individual genotypes and is associated with 1 phenotype.

Variation displays