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:136045293 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1256 individual genotypes.

Variation displays