Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: < 0.01 (T)
Location

Chromosome 19:5831880 (forward strand)|View in location tab

Most severe consequence
 
Stop gained
Evidence status

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 24 transcripts, has 2810 sample genotypes and is mentioned in 4 citations.

Variant displays