Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.46 (A)
Location

Chromosome 6:39357302 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM074911

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4444 sample genotypes and is mentioned in 39 citations.

Variant displays