Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.03 (A)
Location

Chromosome X:136144798 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.136144798G>A

About this variant

This variant overlaps 10 transcripts and has 2504 sample genotypes.

Variant displays