Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.04 (G)
Location

Chromosome X:152952825 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59978887

This variation has 8 HGVS names - click the plus to show

Variation displays