Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome X:19343843 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs7059222

HGVS name

X:g.19343843G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays