Original source

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

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

Chromosome 19:11382706 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and 1 regulatory feature.

Variant displays