Original source

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

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

Chromosome 13: between 48231521 and 48231522 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.48231521_48231522insTTTG

Variation displays