Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.07 (G)
Location

Chromosome 6:111580250 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 6 synonyms - click the plus to show

This variant has 14 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 2511 sample genotypes and is mentioned in 2 citations.

Variant displays