Original source

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

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

Chromosome X:48901944 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061925

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7421, 2010_April_001_315_PQBP1_300463_0007

This variation has 25 HGVS names - click the plus to show

Variation displays