Original source

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

Alleles
T/C | Ambiguity code: Y | MAF: 0.02 (C)
Location

Chromosome X:38322877 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM011007 ; PhenCode RPGR_00205 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5

Variation displays