Original source

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

Alleles
-/TT/TTTT
Location

Chromosome 5: between 132869132 and 132869133 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34655494

This variation has 2 HGVS names - click the plus to show

Variation displays