Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/T | Ancestral: C | Ambiguity code: K
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs524885

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2 individual genotypes.

Variation displays