Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.19 (C)
Location

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

Most severe consequence
Evidence status

Synonyms

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

Variation displays