Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.10 (A)
Location

Chromosome 19:33391316 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms
HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 14 transcripts, has 3663 sample genotypes and is mentioned in 1 citation.

Variant displays