Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.21 (G)
Location

Chromosome 1:39639142 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386613579, rs58515555

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

Variant displays