Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:38367347 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910274

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7392, OTC_AAA0000029

This variation has 5 HGVS names - click the plus to show

Variation displays