Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.26 (T)
Location

Chromosome X:72677453 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17312213, rs59912223

This variation has 6 HGVS names - click the plus to show

Variation displays