Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.24 (A)
Location

Chromosome 16:3590273 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 4154 sample genotypes and is mentioned in 1 citation.

Variant displays