Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.19 (A)
Location

Chromosome 4:3485424 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs59436970

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2527 individual genotypes.

Variation displays