Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/T|Ancestral: C|Ambiguity code: K|MAF: 0.48 (T)
Location

Chromosome X:151397088 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs524885

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays