Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.45 (G)
Location

Chromosome X:2934910 (forward strand) | View in location tab

Co-located

with dbSNP rs74787451 (G/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3747398, rs3175224

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays