Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome X:38178162 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961257 ; PhenCode RISN_RPGR:c.389T>G (A/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8441, RISN-RPGR:c.389T>G

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

Variation displays