Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome X:134475197 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM900133, CM830001

Most severe consequence
Clinical significance

Synonyms

LSDB 8292, 8293

This variation has 10 HGVS names - click the plus to show

Variation displays