Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome X:154046529 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60248475, rs61484111

This variation has 17 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 17 transcripts, has 1360 individual genotypes and is mentioned in 13 citations.

Variation displays