Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.11 (G)
Location

Chromosome X:82764042 (forward strand) | View in location tab

Co-located

with COSMIC COSM1180653 (G/C)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad

Variation displays