Original source

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

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

Chromosome X:136167098-136167101 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs143563921

This variation has 8 HGVS names - click the plus to show

Variation displays