Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.05 (A)
Location

Chromosome 4:87982622 (forward strand)|View in location tab

Co-located variant

dbSNP rs772321959 (G/-)

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

Variant displays