Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R
Location

Chromosome X:135983290 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60088348

HGVS name

X:g.135983290G>A

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1523 sample genotypes.

Variant displays