Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and 1 regulatory feature.

Variant displays