Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.45 (A)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60248475, rs61484111

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 16 transcripts, 1 regulatory feature, has 3864 sample genotypes and is mentioned in 13 citations.

Variant displays