Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:38163999 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961262 ; PhenCode RISN_RPGR:c.823G>A (C/T), RPGR_00020 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8443, RISN-RPGR:c.823G>A

This variation has 21 HGVS names - click the plus to show

Variation displays