Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 19:1220503 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Stop gained
Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and 1 regulatory feature.

Variant displays