Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R
Location

Chromosome X:2934197 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.2934197A>G

About this variant

This variant overlaps 8 transcripts.

Variant displays