Original source

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

Alleles
T/A/G|Ancestral: G|Ambiguity code: D|MAF: 0.20 (T)
Location

Chromosome 19:8977341 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4035 sample genotypes and is mentioned in 1 citation.

Variant displays