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: 0.08 (A)
Location

Chromosome X:135983290 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60088348

HGVS name

X:g.135983290G>A

This variation has assays on 7 chips - click the plus to show

Variation displays