Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome X:154770804 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990479

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 28 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays