Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.48 (T)
Location

Chromosome X:153311980 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60248475, rs61484111

This variation has 11 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

Variation displays