Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 17:56594242 (forward strand) | View in location tab

Most severe consequence
 
Frameshift variant

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and 1 regulatory feature.

Variant displays