Original source

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

Alleles
-/CACCTT/CACCTTCACCTT
Location

Chromosome 13: between 113296617 and 113296618 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 3 transcripts and has 1 individual genotype.

Variation displays