Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.01 (T)
Location

Chromosome X:135984665 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.135984665G>T

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays