Original source

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

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

Chromosome X:134458663 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.134458663G>A

About this variant

This variant overlaps 2 transcripts.

Variation displays