Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 19:5830431 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

19:g.5830431delC

About this variant

This variant overlaps 12 transcripts.

Variant displays