Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.01 (T)
Location

Chromosome X:134458937 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.134458937A>T

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays