Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 6:52438563 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 5 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2510 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays