Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 1:7773966 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 3 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3694 sample genotypes and is associated with 1 phenotype.

Variant displays