Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome X:38169943 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961260 ; PhenCode RISN_RPGR:c.703C>T (G/A), RPGR_00016 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB RISN-RPGR:c.703C>T, 8442

This variation has 20 HGVS names - click the plus to show

Variation displays