Original source

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

Alleles
TTG/- | MAF: 0.29 (-)
Location

Chromosome X:150566881-150566883 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146948708

This variation has 4 HGVS names - click the plus to show

Variation displays