Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.02 (G)
Location

Chromosome X:134458535 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.134458535T>G

About this variant

This variant overlaps 2 transcripts and has 2925 sample genotypes.

Variant displays