Original source

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

Alleles
TGTGTGTG/-
Location

Chromosome X:37795899-37795906 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs36208183

This variation has 5 HGVS names - click the plus to show

Variation displays