Original source

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

Alleles
T/-
Location

Chromosome X:48756083 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72149965

This variation has 19 HGVS names - click the plus to show

Variation displays