Original source

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

C/G | Ancestral: G | Ambiguity code: S

Chromosome X:48578119 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs235828, rs57895036, rs3174406

This variation has 3 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts and has 1242 individual genotypes.

Variation displays