Original source

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

Alleles
G/T | Ambiguity code: K
Location

Chromosome X:38321041 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992210 ; PhenCode RISN_RPGR:c.296C>A (G/T), RPGR_00006 (G/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8449, RISN-RPGR:c.296C>A

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

Variation displays