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: 0.46 (A)
Location

Chromosome X:9725303 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2074094, rs57003678

HGVS name

X:g.9725303G>A

This variation has assays on 9 chips - click the plus to show

Variation displays