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: 0.08 (A)
Location

Chromosome X:83509032 (forward strand) | View in location tab

Co-located

with dbSNP rs111919890 (A/-)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs58335216

This variation has 2 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays