Original source

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

Alleles
-/TGTT
Location

Chromosome 1: between 183524638 and 183524639 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140052983, rs34919085

This variation has 3 HGVS names - click the plus to show

Variation displays