Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 19:1213912 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature and has 9 sample genotypes.

Variant displays