Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.34 (T)
Location

Chromosome X:48523786 (forward strand) | View in location tab

Co-located

with COSMIC COSM150788 (G/T)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

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

Variation displays