Original source

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

Alleles
-/T/TT/TTT
Location

Chromosome 1: between 43336293 and 43336294 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs67970479, rs67970478

This variation has 6 HGVS names - click the plus to show

Variation displays