Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.39 (A)
Location

Chromosome X:133304844 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

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

Variation displays