Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.42 (T)
Location

Chromosome X:46858276 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59286713, rs17323126

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

Variation displays