Original source

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

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

Chromosome X:135984769 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.135984769G>T

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts and has 268 sample genotypes.

Variant displays