Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome 19:33387137 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and has 5 sample genotypes.

Variant displays