Original source

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

Alleles
-/TTTG | MAF: 0.03 (TTTG)
Location

Chromosome 13: between 48805657 and 48805658 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.48805657_48805658insTTTG

Variation displays