Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.09 (G)
Location

Chromosome X:100988470 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60295890

This variation has 7 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays