Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 19:10292262 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 6 synonyms - Show

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2567 sample genotypes and is mentioned in 3 citations.

Variant displays