Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.10 (T)
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 1095 individual genotypes and is associated with 1 phenotype.

Variation displays