Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome X:48523858 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990494

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_083_EBP_300205_0001, 6912

This variation has 9 HGVS names - click the plus to show

Variation displays