This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
T/A/C/G|Ancestral: G|Ambiguity code: N|MAF: 0.32 (T)
Location

Chromosome 8:132888007 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 7 synonyms - Show

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4301 sample genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays