Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 19:49064554 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays