Original source

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

Alleles
TTTT/-
Location

Chromosome 2:112838692-112838695 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs142617044, rs35745590

HGVS name

2:g.112838692_112838695delTTTT

Variation displays