Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:154768338 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52791944

This variation has 16 HGVS names - click the plus to show

Genotyping chips

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

Variation displays