Original source

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

Alleles
C/A | Ambiguity code: M
Location

Chromosome X:38322921 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971311 ; PhenCode RISN_RPGR:c.179G>T (C/A), RPGR_00004 (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8446, RISN-RPGR:c.179G>T

This variation has 12 HGVS names - click the plus to show

Variation displays