Original source

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

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

Chromosome X:43603735 (forward strand) | View in location tab

Co-located

with COSMIC COSM1121508 (A/C)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_014796

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays