Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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