Original source

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

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

Chromosome 4:3503721 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

This variant has 2 HGVS names - click the plus to show

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 3972 sample genotypes and is mentioned in 1 citation.

Variant displays