Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/TTTG | MAF: 0.02 (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

About this variant

This variant overlaps 3 transcripts and has 2504 individual genotypes.

Variation displays