Original source

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

Alleles
TT/-/TTT/TTTTT
Location

Chromosome 1:150693848-150693849 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72035116, rs66627373

This variation has 9 HGVS names - click the plus to show

Variation displays