Original source

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

Alleles
AGTG/- | MAF: 0.37 (AGTG)
Location

Chromosome X:135249257-135249260 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs143563921

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

Variation displays