Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome X:48898800 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72149965

This variation has 18 HGVS names - click the plus to show

Variation displays